Publications prior to 2010

2009

[338] Asymmetric pentenylation of aldehydes: A new benchmark for the preparation of ethyl-substituted homoallylic alcohol. R. P. Sonawane, S. R. Joolakanti, S. Arseniyadis, J. Cossy Synlett 2009, 213-216.

[337] Highly enantioselective synthesis of linear beta-amino alcohols. T. X. Metro, D. Gomez Pardo, J. Cossy Chemistry - A Eur. J. 2009, 15, 1064-1070.

[336] A versatile route to the tulearin class of macrolactones: Synthesis of a stereoisomer of tulearin A. A. L. Mandel, V. Bellosta, D. P. Curran, J. Cossy Org. Lett. 2009, 11, 3282-3285.

[335] Straightforward synthesis of the near-infrared fluorescent voltage-sensitive dye
RH1691 and analogues thereof
. R. Lebeuf, I. Ferezou, J. Rossier, S. Arseniyadis, J. Cossy Org. Lett. 2009, 11, 4822-4825.

[334] Daucus carota-mediated reduction of cyclic 3-oxo-amines. R. Lacheretz, D. Gomez Pardo, J. Cossy Org. Lett. 2009, 11, 1245-1248.

[333] Enantioselective organocatalytic conjugate reduction of beta-azole-containing alpha,beta-unsaturated aldehydes. T. J. Hoffman, J. Dash, J. H. Rigby, S. Arseniyadis, J. Cossy Org. Lett. 2009, 11, 2756-2759.

[332] Diastereodivergent addition of allenylzincs to aryl glyoxylates. T. Hameury, J. Guillemont, L. Van Hijfte, V. Bellosta, J. Cossy Org. Lett. 2009, 11, 2397-2400.

[331] Acryloyl chloride: An excellent substrate for cross-metathesis. A one-pot sequence for the synthesis of substituted alpha,beta-unsaturated carbonyl derivatives. L. Ferrie, S. BouzBouz, J. Cossy Org. Lett. 2009, 11, 5446-5448.

[330] Rearrangement of N-alkyl 1,2-amino alcohols. Synthesis of (S)-toliprolol and (S)-propanolol. B. Duthion, T. X. Metro, D. Gomez Pardo, J. Cossy Tetrahedron 2009, 65, 6696-6706.

[329] A convergent approach toward the C1-C11 subunit of phoslactomycins and formal synthesis of phoslactomycin B. V. Druais, M. J. Hall, C. Corsi, S. V. Wendeborn, C. Meyer, J. Cossy Org. Lett. 2009, 11, 935-938.

[328] Gold-catalyzed cycloisomerizations of ene-ynamides. S. Couty, C. Meyer, J. Cossy Tetrahedron 2009, 65, 1809-1832.

[327] Convergent synthesis of the C18-C30 fragment of amphidinol 3. J. Cossy, T. Tsuchiya, S. Reymond, T. Kreuzer, F. Colobert, I. E. Marko Synlett 2009, 2706-2710.

[326] Rearrangement of beta-amino alcohols and application to the synthesis of biologically active compounds. J. Cossy, D. Gomez Pardo, C. Dumas, O. Mirguet, I. Dechamps, T. X. Metro, B. Burger, R. Roudeau, J. Appenzeller, A. Cochi Chirality 2009, 21, 850-856.

[325] Enantioselective ring expansion of prolinols: An efficient and short synthesis of 2-phenylpiperidin-3-ol derivatives and 3-hydroxypipecolic acids. A. Cochi, B. Burger, C. Navarro, D. Gomez Pardo, J. Cossy, Y. Zhao, T. Cohen Synlett 2009, 2157-2161.

[324] Iron trichloride-promoted cyclization of o-alkynylaryl isocyanates: Synthesis of 3-(chloromethylene)oxindoles. G. Cantagrel, B. de Carne-Carnavalet, C. Meyer, J. Cossy Org. Lett. 2009, 11, 4262-4265.

[323] One-pot hydrosilylation-RCM-protodesilylation: Application to the synthesis of omega-alkenyl alpha,beta-unsaturated lactones. C. Bressy, F. Bargiggia, M. Guyonnet, S. Arseniyadis, J. Cossy Synlett 2009, 565-568.

[322] Simple synthesis of conjugated all-(E)-polyenic aldehydes, ketones, and esters using chemoselective cross-metathesis and an iterative sequence of reactions: Application to the synthesis of navenone B. S. BouzBouz, C. Roche, J. Cossy Synlett 2009, 803-807.

[321] FeCl3-catalyzed Ritter reaction. Synthesis of amides. B. Anxionnat, A. Guérinot, S. Reymond, J. Cossy Tetrahedron Lett. 2009, 50, 3470-3473.

[320] Synthesis of two bioactive natural products: FR252921 and pseudotrienic acid B. D. Amans, V. Bellosta, J. Cossy Chemistry - A Eur. J. 2009, 15, 3457-3473.

[319] Synthesis of the monomeric counterpart of marinomycin A. D. Amans, L. Bareille, V. Bellosta, J. Cossy J. Org. Chem. 2009, 74, 7665-7674.

2008

[318] Une source potentielle d’anticancéreux : Les produits naturels et leurs analogues. Extraction, caractérisation, activité biologique et synthèse. J. Cossy Comptes Rendus Chimie 2008, 11, 1303-1305.

[317] A convergent total synthesis of (+)-febrifugine. B. Sieng, O. L. Ventura, V. Bellosta, J. Cossy Synlett 2008, 1216-1218.

[316] Synthetic studies toward cytostatin, a natural product inhibitor of protein phosphatase 2A. A. F. Salit, C. Meyer, J. Cossy, B. Delouvrie, L. Hennequin Tetrahedron 2008, 64, 6684-6697.

[315] Synthesis of gamma-alkylidene alpha,beta-unsaturated delta-lactones by ring-closing metathesis: Application to the synthesis of the C1-C8 subunit of biselide E. A. F. Salit, M. Barbazanges, F. Miege, M. H. Larraufie, C. Meyer, J. Cossy Synlett 2008, 2583-2586.

[314] Chemoselective reactions: Toward the synthesis of biologically active natural products with anticancer activities. S. Reymond, L. Ferrie, A. Guérinot, P. Capdevielle, J. Cossy Pure and Applied Chemistry 2008, 80, 1683-1691.

[313] Copper-catalyzed Diels-Alder reactions. S. Reymond, J. Cossy Chem. Rev. 2008, 108, 5359-5406.

[312] Migrastatin and analogues: New anti-metastatic agents. S. Reymond, J. Cossy Comptes Rendus Chimie 2008, 11, 1447-1462.

[311] Formal synthesis of leustroducsin B. J. Moise,R. P. Sonawane, C. Corsi, S. V. Wendeborn, S. Arseniyadis, J. Cossy Synlett 2008, 2617-2620.

[310] Syntheses of (S,S)-reboxetine via a catalytic stereospecific rearrangement of beta-amino alcohols. T. X. Metro, D. Gomez Pardo, J. Cossy J. Org. Chem. 2008, 73, 707-710.

[309] Synthesis of vinyl-functionalized oxazoles by olefin cross-metathesis. T. J. Hoffman, J. H. Rigby, S. Arseniyadis, J. Cossy J. Org. Chem. 2008, 73, 2400-2403.

[308] [1,2]-Wittig rearrangement of (benzyloxy)acetamides. T. Hameury, J. Guillemont, L. Van Hijfte, V. Bellosta, J. Cossy Synlett 2008, 2345-2347.

[307] Facile synthesis of the C1-C13 fragment of lyngbouilloside. J. Gebauer, S. Arseniyadis, J. Cossy Synlett 2008, 712-714.

[306] Total synthesis of cystothiazole a by microwave-assisted olefin cross-metathesis. J. Gebauer, S. Arseniyadis, J. Cossy Eur. J. Org. Chem. 2008, 2701-2704.

[305] Neopeltolide, a new promising antitumoral agent. J. Gallon, S. Reymond, J. Cossy Comptes Rendus Chimie 2008, 11, 1463-1476.

[304] Synthetic efforts toward the macrolactone core of leucascandrolide A. L. Ferrie, L Boulard, F. Pradaux, S. BouzBouz, S. Reymond, P. Capdevielle, J. Cossy J. Org. Chem. 2008, 73, 1864-1880.

[303] Total Synthesis of (+)-Dodoneine. A. Dittoo, V. Bellosta, J. Cossy Synlett 2008, 2459-2460.

[302] Synthetic efforts toward the synthesis of octalactins. M. T. Dinh, S. BouzBouz, J. L. Peglion, J. Cossy Tetrahedron 2008, 64, 5703-5710.

[301] Exiguolide, a simplified analogue of the bryostatins by Nature ? J. Cossy Comptes Rendus Chimie 2008, 11, 1477-1482.

[300] A potential source for anticancer agents: Natural products and analogues. Extraction, characterization, biological activity and synthesis. J. Cossy Comptes Rendus Chimie 2008, 11, 1303-1305.

[299] Asymmetric total synthesis of the immunosuppressant (-)-pironetin. C. Bressy, J. P. Vors, S. Hillebrand, S. Arseniyadis, J. Cossy Angew. Chem., Int. Ed. 2008, 47, 10137-10140.

[298] Synthesis of optically enriched 1,2-amino alcohols by [2,3]-Wittig rearrangements of 3-aza-allylic alcohol derivatives. M. Barbazanges, C. Meyer, J. Cossy Tetrahedron Lett. 2008, 49, 2902-2906.

[297] Total Synthesis of Amphidinolide J. M. Barbazanges, C. Meyer, J. Cossy Org. Lett. 2008, 10, 4489-4492.

2007

[296] Synthesis of 3-oxooxa- and 3-oxoazacycloalk-4-enes by ring-closing metathesis. Application to the synthesis of an inhibitor of cathepsin K. C. Taillier, T. Hameury, V. Bellosta, J. Cossy Tetrahedron 2007, 63, 4472-4490.

[295] Formal synthesis of cytostatin by a convergent approach. A. F. Salit, C. Meyer, J. Cossy Synlett 2007, 934-938.

[294] Synthesis of migrastatin and its macrolide core. S. Reymond, J. Cossy Tetrahedron 2007, 63, 5918-5929.

[293] Cross-metathesis between α-methylene-γ-butyrolactone and olefins: A dramatic additive effect. J. Moise, S. Arseniyadis, J. Cossy Org. Lett. 2007, 9, 1695-1698.

[292] Highly enantioselective synthesis of β-amino alcohols:  A catalytic version. T. X. Metro, D. Gomez Pardo, J. Cossy J. Org. Chem. 2007, 72, 6556-6561.

[291] Stereospecific rearrangement of beta-amino alcohols catalyzed by H2SO4. T. X. Metro, D. Gomez Pardo, J. Cossy Synlett 2007, 2888-2890.

[290] Studies on enol carbonate chemistry: Stereoselective construction of vicinal quaternary benzylic centers in the bis-oxindole series. C. Menozzi, P. I. Dalko, J. Cossy Heterocycles 2007, 72, 199-205.

[289] Iron-catalyzed cross-coupling of alkyl halides with alkenyl Grignard reagents. A. Guérinot, S. Reymond, J. Cossy Angew. Chem., Int. Ed. 2007, 46, 6521-6524.

[288] A concise total synthesis of melithiazole C. J. Gebauer, S. Arseniyadis, J. Cossy Org. Lett. 2007, 9, 3425-3427.

[287] Formal chemoselective synthesis of leucascandrolide A. L. Ferrie, S. Reymond, P. Capdevielle, J. Cossy Org. Lett. 2007, 9, 2461-2464.

[286] Concise total synthesis of (-)-muricatacin and (-)-iso-cladospolide B using chemoselective cross-metathesis. L. Ferrie, S. Reymond, P. Capdevielle, J. Cossy Synlett 2007, 2891-2893.

[285] Synthesis of optically active substituted 3-fluoropiperidines from prolinols by Using DAST. I. Dechamps, D. Gomez Pardo, J. Cossy Synlett 2007, 263-267.

[284] Enantioselective ring expansion of prolinols and ring-closing metathesis: formal synthesis of (-)-swainsonine. I. Dechamps, D. Gomez Pardo, J. Cossy Arkivoc 2007, 38-45.

[283] Ring expansion induced by DAST: Synthesis of substituted 3-fluoropiperidines from prolinols and 3-fluoroazepanes from 2-hydroxymethylpiperidines. I. Dechamps, D. Gomez Pardo, J. Cossy Eur. J. Org. Chem. 2007, 4224-4234.

[282] Enantioselective ring expansion of prolinol derivatives. Two formal syntheses of (-)-swainsonine. I. Dechamps, D. Gomez Pardo, J. Cossy Tetrahedron 2007, 63, 9082-9091.

[281] Synthesis of vinyl-functionalized thiazoles by cross-metathesis and tandem Stille coupling/cross-metathesis. J. Dash, S. Arseniyadis, J. Cossy Adv. Synth. & Catal. 2007, 349, 152-156.

[280] Chemoselective epoxidation of ene-ynamides: Intramolecular cyclopropanation induced by the intermediate α-oxocarbene. S. Couty, C. Meyer, J. Cossy Synlett 2007, 2819-2822.

[279] Efficient syntheses of the polyene fragments present in amphidinols. J. Cossy, T. Tsuchiya, L. Ferrie, S. Reymond, T. Kreuzer, F. Colobert, P. Jourdain, I. E. Marko Synlett 2007, 2286-2288.

[278] Stereoselective synthesis of the C53-C67 polyene fragment of amphidinol 3. F. Colobert, T. Kreuzer, J. Cossy, S. Reymond, T. Tsuchiya, L. Ferrie, I. E. Marko, P. Jourdain Synlett 2007, 2351-2354.

[277] Synthetic studies towards the marine natural product palmerolide A: synthesis of the C3-C15 and C16-C23 fragments. G. Cantagrel, C. Meyer, J. Cossy Synlett 2007, 2983-2986.

[276] Total synthesis of herbimycin A. S. Canova, V. Bellosta, A. Bigot, P. Mailliet, S. Mignani, J. Cossy Org. Lett. 2007, 9, 145-148.

[275] Ruthenium-catalyzed cross-metathesis between diallylsilanes and electron-deficient Olefins. S. BouzBouz, L. Boulard, J. Cossy Org. Lett. 2007, 9, 3765-3768.

[274] Synthesis of the C1-C13 fragment of (+)-callipeltoside A. L. Boulard, S. BouzBouz, J. M. Paris, J. Cossy Synlett 2007, 1461-1463.

[273] Highly diastereoselective addition of phenyllithium on cis-substituted C-cyclopropylaldimines. D. Belotti, N. Noujeim, J. Cossy Synlett 2007, 259-262.

[272] Stereoselective synthesis of 1,2-aminoalcohols by [2,3]-Wittig rearrangements. M. Barbazanges, C. Meyer, J. Cossy Org. Lett. 2007, 9, 3245-3248.

[271] Synthesis of an analog of mycothiazole and total synthesis of pseudotrienic acid B. D. Amans, A. Le Flohic, V. Bellosta, C. Meyer, J. Cossy Pure and Applied Chemistry 2007, 79, 677-684.

[270] An efficient and stereoselective synthesis of the monomeric counterpart of marinomycin A. D. Amans, V. Bellosta, J. Cossy Org. Lett. 2007, 9, 1453-1456.

[269] Synthesis of a promising immunosuppressant: FR252921. D. Amans, V. Bellosta, J. Cossy Org. Lett. 2007, 9, 4761-4764.

[268] A short and highly diastereoselective synthesis of verbalactone. F. Allais, M. C. Louvel, J. Cossy Synlett 2007, 451-452.

2006

[267] Synthesis of 3-oxoazacyclohept-4-enes by ring-closing metathesis. Application to the synthesis of an inhibitor of cathepsin K. C. Taillier, T. Hameury, V. Bellosta, J. Cossy Heterocycles 2006, 67, 549-554.

[266] Enantioselective diethylzinc addition to aromatic and aliphatic aldehydes using (3R,5R)-dihydroxypiperidine derivatives catalyst. R. D. Roudeau, Gomez Pardo, J. Cossy Tetrahedron 2006, 62, 2388-2394.

[265] Total synthesis of (+)-migrastatin. S. Reymond, J. Cossy Eur. J. Org. Chem. 2006, 4800-4804.

[264] Highly enantioselective synthesis of beta-amino alcohols. T. X. Metro, J. Appenzeller, D. Gomez Pardo, J. Cossy Org. Lett. 2006, 8, 3509-3512.

[263] Concise synthesis of the (+/-)-N-b-desmethyl-meso-chimonanthine. C. Menozzi, P. I. Dalko, J. Cossy. Chem. Commun. 2006, 4638-4640.

[262] Ring expansion of functionalized octahydroindoles to enantiopure cis-decahydroquinolines. M. Mena, J. Bonjoch, D. Gomez Pardo, J. Cossy J. Org. Chem. 2006, 71, 5930-5935.

[261] Reactivity of unsaturated sultones synthesized from unsaturated alcohols by ring-closing metathesis. Application to the racemic synthesis of the originally proposed structure of mycothiazole. A. Le Flohic, C. Meyer, J. Cossy Tetrahedron 2006, 62, 9017-9037.

[260] Total synthesis of (-)-spongidepsin. L. Ferrie, S. Reymond, P. Capdevielle, J. Cossy Org. Lett. 2006, 8, 3441-3443.

[259] Chemoselective cross-metathesis reaction between electron-deficient 1,3-dienes and olefins. L. Ferrie, D. Amans, S. Reymond, V. Bellosta, P. Capdevielle, J. Cossy J. Organomet. Chem. 2006, 691, 5456-5465.

[258] A short synthesis of lennoxamine via ynamides. S. Couty, C. Meyer, J. Cossy Tetrahedron Lett. 2006, 47, 767-769.

[257] Diastereoselective gold-catalyzed cycloisomerizations of ene-ynamides. S. Couty, C. Meyer, J. Cossy Angew. Chem., Int. Ed. 2006, 45, 6726-6730.

[256] Synthesis of 3-(arylmethylene)isoindolin-1-ones from ynamides by Heck-Suzuki-Miyaura domino reactions. Application to the synthesis of lennoxamine. S. Couty, B. Liegault, C. Meyer, J. Cossy Tetrahedron 2006, 62, 3882-3895.

[255] Biological evaluation of newly synthesized quinoline-5,8-quinones as Cdc25B inhibitors. J. Cossy, D. Belotti, M. Brisson, J. J. Skoko, P. Widf, J. S. Lazo Bioorg. Med. Chem. 2006, 14, 6283-6287.

[254] Generation of ketyl radical anions by photoinduced electron transfer (PET) between ketones and amines. Synthetic applications. J. Cossy, D. Belotti Tetrahedron 2006, 62, 6459-6470.

[253] Jean Rigaudy (1921-2005) - Hommage. J. Cossy Actualite Chimique 2006, 136-136.

[252] Rearrangement of homoallylic alcohols induced by DAST. S. Canova, V. Bellosta, S. Mignani, A. Bigot, J. Cossy Org. Lett. 2006, 8, 2091-2094.

[251] A short and efficient synthesis of (-)-diospongin A. C. Bressy, F. Allais, J. Cossy Synlett 2006, 3455-3456.

[250] Two approaches for efficient synthesis of (-)-colletol. S. BouzBouz, J. Cossy Tetrahedron Lett. 2006, 47, 901-904.

[249] Desymmetrization of substituted 1,3-diketones: A formal synthesis of (+)-stemoamide. N. Bogliotti, P. I. Dalko, J. Cossy Synlett 2006, 2664-2666.

[248] Free-radical approaches to stemoamide and analogues. N. Bogliotti, P. I. Dalko, J. Cossy J. Org. Chem. 2006, 71, 9528-9531.

[247] Total synthesis of pseudotrienic acid B: A bioactive metabolite from Pseudomonas sp MF 381-IODS. D. Amans, V. Bellosta, J. Cossy Angew. Chem., Int. Ed. 2006, 45, 5870-5874.

[246] Enantio- and diastereoselective allylmetalations: An easy and efficient access to the AB spiroketal of spongistatin. F. Allais, J. Cossy Org. Lett. 2006, 8, 3655-3657.

2005

[245] Hydrosilylation of terminal alkynes with alkylidene ruthenium complexes and silanes. C. Menozzi, P. I. Dalko, J. Cossy J. Org. Chem. 2005, 70, 10717-10719.

[244] In memoriam to Anne Ghosez-Giese. C. Chatgilialoglu, J. Cossy, D. P. Curran, K. B. Sharpless, and H. Yamamoto Synlett 2005, 2835-2835.

[243] A short and efficient stereoselective synthesis of the octalactin lactone using enantioselective crotyltitanations and a cross-metathesis reaction
M. T. Dinh, S. BouzBouz, J. L. Peglion, J. Cossy Synlett 2005, 2851-2853.

[242] Short synthesis of the selective Rho-kinase inhibitor Y-27632 and of its enantiomer. D. Belotti, J. L. Peglion, J. Cossy Lett. Org. Chem. 2005, 2, 634-636.

[241] Reduction of olefins using ruthenium carbene catalysts and silanes.
C. Menozzi, P. I. Dalko, J. Cossy Synlett 2005, 2449-2452.

[240] A one-pot process for the enantioselective preparation of saturated secondary alcohols from propargyl ketones under hydrogen transfer conditions.
N. Bogliotti, P. I. Dalko, J. Cossy Tetrahedron Lett. 2005, 46, 6915-6918.

[239] Regioselective synthesis of 1,2-and 1,3-diols from omega-hydroxy allyl acetates and carbonates via Pd complexes using boric acid and trialkyl borates. J. Cluzeau, P. Capdevielle, J. Cossy Tetrahedron Lett. 2005, 46, 6945-6948.

[238] Synthesis of polypropionate subunits from cyclopropanes. M. Defosseux, N. Blanchard, C. Meyer, J. Cossy Tetrahedron 2005, 61, 7632-7653.

[237] A short and enantioselective synthesis of colletodiol. L. Ferrie, P. Capdevielle, J. Cossy Synlett 2005, 1933-1935.

[236] Total synthesis of zincophorin. J. Cossy, C. Meyer, M. Defosseux, N. Blanchard Pure and Applied Chemistry 2005, 77, 1131-1137.

[235] Efficient enantioselective formal synthesis of Ro 67-8867, a NMDA 2B receptor antagonist. I. Dechamps, D. G. Pardo, P. Karoyan, J. Cossy Synlett 2005, 1170-1172.

[234] Palladium-catalyzed Suzuki-Miyaura coupling reactions involving beta,beta-dihaloenamides: Application to the synthesis of disubstituted ynamides. S. Couty, M. Barbazanges, C. Meyer, J. Cossy Synlett 2005, 905-910.

[233] Synthetic approaches and total synthesis of natural zoapatanol. C. Taillier, B. Gille, V. Bellosta, J. Cossy J. Org. Chem. 2005, 70, 2097-2108.

[232] A very short and efficient synthesis of preclamol. A. de Filippis, D. Gomez Pardo, J. Cossy Lett. Org. Chem. 2005, 2, 136-138.

[231] A radical approach for the construction of the tricyclic core of stemoamide. N. Bogliotti, P. I. Dalko, J. Cossy Synlett 2005, 349-351.

[230] A one-pot Reformatsky/cyclopropanation sequence induced by diethylzinc. M. F. Laroche, D. Belotti, J. Cossy Org. Lett. 2005, 7, 171-173.

[229] Total synthesis of ((+)(-))-mycothiazole and formal enantioselective approach. A. Le Flohic, C. Meyer, J. Cossy Org. Lett. 2005, 7, 339-342.

[228] Selective methodologies for the synthesis of biologically active piperidinic compounds. J. Cossy Chemical Records 2005, 5, 70-80.

[227] Metathesis reactions. General considerations. P. Van de Weghe, J. Eustache, J. Cossy Current Topics in Medicinal Chemistry 2005, 5, 1461-1472.

[226] Hydrogenation versus hydrogenolysis with a safe, selective and reusable catalyst: palladium black on Teflon (R). D. Belotti, G. Cantagrel, C. Combellas, J. Cossy, F. Kanoufi, S. Nunige New J. Chem. 2005, 29, 761-764.

2004

[225] Simple preparation of 3-aryl 2-piperidinones. A. de Filippis, D. Gomez Pardo, J. Cossy Synthesis 2004, 2930-2933.

[224] Palladium-catalyzed alpha-arylation of N-protected 2-piperidinones. A. de Filippis, D. Gomez Pardo, J. Cossy Tetrahedron 2004, 60, 9757-9767.

[223] Regioselective cross-metathesis reaction induced by steric hindrance. S. BouzBouz, R. Simmons, J. Cossy Org. Lett. 2004, 6, 3465-3467.

[222] Tetrafibricin: Synthesis of the C1-C13, C15-C25, and C27-C40 fragments. S. BouzBouz, J. Cossy Org. Lett. 2004, 6, 3469-3472.

[221] Stereoselective synthesis of the C15-C24 fragment of discodermolide by desymmetrization of a meso dialdehyde. S. BouzBouz, J. Cossy Synlett 2004, 2034-2036.

[220] Two successive one-pot reactions leading to the expeditious synthesis of (-)-centrolobine. L. Boulard, S. BouzBouz, J. Cossy, X. Franck, B. Figadere Tetrahedron Lett. 2004, 45, 6603-6605.

[219] Total synthesis of (+)-preussin: Control of the stereogenic centers by enantioselective allyltitanations. S. Canova, V. Bellosta, J. Cossy Synlett, 2004, 10, 1811-1813.

[218] Heck-Suzuki-Miyaura domino reactions involving ynamides. An efficient access to 3-(Arylmethylene)isoindolinones. S. Couty, B. Liegault, C. Meyer, J. Cossy Org. Lett. 2004, 6, 2511-2514.

[217] Total synthesis of zincophorin and its methyl ester. M. Defosseux, N. Blanchard, C. Meyer, J. Cossy J. Org. Chem. 2004, 69, 4626-4647.

[216] Synthesis of omega-hydroxy ketones from omega-benzyloxy Weinreb amides by using a chemoselective nucleophilic addition/birch reduction process. C. Taillier, V. Bellosta, C. Meyer, J. Cossy Org. Lett. 2004, 6, 2145-2147.

[215] Total synthesis of natural (+)-(2’S,3’R)-zoapatanol. C. Taillier, V. Bellosta, J. Cossy Org. Lett. 2004, 6, 2149-2151.

[214] Natural (5 ’-oxoheptene-1 ’ E,3 ’ E-dienyl)-5,6-dihydro-2H-pyran-2-one: total synthesis and revision of its absolute configuration. S. BouzBouz, E. de Lemos, J. Cossy, J. Saez, X. Franck, B. Figadere Tetrahedron Lett. 2004, 45, 2615-2617.

[213] Modular ligands in asymmetric synthesis. Copper-mediated cyclopropanation. D. Tepfenhart, L. Moisan, P. I. Dalko, J. Cossy Tetrahedron Lett. 2004, 45, 1781-1783.

2003

[212] Synthesis of the C14-C25 Subunit of Bafilomycin A1. F. Eustache, P. I. Dalko, J. Cossy J. Org. Chem. 2003, 68, 9994.

[211] Base effect on the palladium catalyzed a-arylation of N-benzyl-2-piperidinones. J. Cossy, A. de Filippis, D. Gomez Pardo Synlett 2003, 2171.

[210] Enantioselective monoreduction of 2-alkyl 1,3-diketones using chiral ruthenium catalysts. Synthesis of the C14-C25 fragment of bafilomycin A1. F. Eustache, P. I. Dalko, J. Cossy Tetrahedron Lett. 2003, 44, 8823.

[209] Stereoselective synthesis of polypropionate units and heterocyclic compounds by cyclopropylcarbinol ring-opening with Mercury(II) salts. C. Meyer, N. Blanchard, M. Deffosseux, J. Cossy Acc. Chem. Res. 2003, 36, 766.

[208] Solid phase synthesis of amides by the Beckmann rearrangement of ketoxime carbonates. S. His, C. Meyer, J. Cossy, G. Emeric, A. Greiner Tetrahedron Lett. 2003, 44, 8581.

[207] Synthesis of unsaturated [1,2]oxazines by using sigmatropic rearrangements and the ring-closing metathesis reaction. A. Le Flohic, C. Meyer, J. Cossy, J. R. Desmurs Tetrahedron Lett. 2003, 44, 8577.

[206] Total synthesis of zincophorin methyl ester. M. Defosseux, N. Blanchard, C. Meyer, J. Cossy Org. Lett. 2003, 5, 4037.

[205] Stereo- and enantioselective reactions. Application to the synthesis of biologically active compounds. J. Cossy, S. BouzBouz, M. Popkin Comptes Rendus Chimie 2003, 6, 547.

[204] Synthesis of indatraline using a Suzuki cross-coupling reaction and a chemoselective hydrogenation: A versatile approach. J. Cossy, D. Belotti, A. Maguer Synlett 2003, 1515.

[203] Stereoselective synthesis of the C1-C13 fragment of (+)-discodermolide using asymmetric allyltitanations. S. BouzBouz, J. Cossy Org. Lett. 2003, 5, 3029.

[202] Palladium-catalyzed intermolecular alpha-arylation of N-protected 2-piperidinones. J. Cossy, A. De Filippis, D. Gomez Pardo Org. Lett. 2003, 5, 3037.

[201] Enantioselective allyltitanations: synthesis of the proposed structures for passifloricin A. S. BouzBouz, J. Cossy Tetrahedron Lett. 2003, 44, 4471.

[200] Total synthesis of (+)-strictifolione. S. BouzBouz, J. Cossy Org. Lett. 2003, 5, 1995.

[199] Unsaturated sultones from unsaturated sulfonates: Synthesis by ring-closing metathesis and reactivity. A. Le Flohic, C. Meyer, J. Cossy, J. R. Desmurs, J. C. Galland Synlett 2003, 667.

[198] [2,3]-Wittig sigmatropic rearrangement of gamma-allyloxy-beta-enaminoesters. I. Pevet, C. Meyer, J. Cossy Synlett 2003, 663.

[197] Radical reactions. Synthesis of heterocyclic compounds. J. Cossy Bulletin de l’Union des Physiciens 2003, 97(851, Cahier 2), 29.

[196] Degradation of aldehydes to one carbon lower homologs. D. Belotti, G. Andreatta, F. Pradaux, S. BouzBouz, J. Cossy Tetrahedron Lett. 2003, 44, 3613.

[195] Tandem cross-metathesis/hydrogenation/cyclization reactions by using compatible catalysts. J. Cossy, F. Bargiggia, S. BouzBouz Org. Lett. 2003, 5, 459.

[194] Diastereoselective conjugate addition of organocuprates to chiral racemic olefinic amido esters. Formal total synthesis of paroxetine. J. Cossy, O. Mirguet, D. Gomez Pardo, J. R. Desmurs New Journal of Chemistry 2003, 27, 475.

2002

[193] A new nitrone from C2 symmetric piperidine for the synthesis of hydroxylated indolizidinone. A. Brandi, S. Cicchi, V. Paschetta, D. Gomez Pardo, J. Cossy Tetrahedron Lett. 2002, 43, 9357.

[192] Synthesis of 3-oxo oxacycloalkenes by ring closing metathesis. J. Cossy, C. Taillier, V. Bellosta Tetrahedron Lett. 2002, 43, 7263.

[191] Regioselective ring opening of epoxides by nucleophiles mediated by lithium bistrifluoromethanesulfonimide. J. Cossy, V. Bellosta, C. Hamoir, J. R. Desmurs Tetrahedron Lett. 2002, 43, 7083.

[190] Tandem reaction by using compatible catalysts: cross-metathesis reaction and hydrogenation. J. Cossy, F. C. Bargiggia, S. BouzBouz Tetrahedron Lett. 2002, 43, 6715.

[189] Formal total synthesis of (+)-methynolide. J. Cossy, D. Bauer, V. Bellosta Tetrahedron 2002, 58, 5909.

[188] Free-radical hydroxylation reactions of alkylboronates. C. Cadot, P. I. Dalko, J. Cossy, C. Ollivier, R. Chuard, P. Renaud J. Org. Chem. 2002, 67, 7193.

[187] A formal synthesis of (-)-paroxetine by enantioselective ring enlargement of a trisubstituted prolinol. J. Cossy, O. Mirguet, D. G. Pardo, J. R. Desmurs Eur. J. Org. Chem. 2002, 3543.

[186] Aromatization of enamines promoted by a catalytic amount of Pd/C. Synthesis of aromatic amines. J. Cossy, D. Belotti Org. Lett. 2002, 4, 2557.

[185] Lithium bistrifluoromethanesulfonimidate-mediated regioselective ring opening of aziridines by amines. J. Cossy, V. Bellosta, V. Alauze, J. R. Desmurs Synthesis 2002, 2211.

[184] A synthetic approach towards the C1-C9 subunit of zincophorin. J. Cossy, N. Blanchard, M. Defosseux, C. Meyer Angew. Chem., Int. Ed. 2002, 41, 2144.

[183] Stereoselective oxymercuration of cyclopropylcarbinols with anchimeric assistance by aromatic groups. J. Cossy, N. Blanchard, C. Meyer Tetrahedron Lett. 2002, 43, 1801.

[182] Olefin isomerization by a ruthenium carbenoid complex. Cleavage of allyl and homoallyl groups. C. Cadot, P. I. Dalko, J. Cossy Tetrahedron Lett. 2002, 43, 1839.

[181] Chiral titanium complexes. Synthesis of optically active unsaturated alcohols, diols, polypropionates and their use in the synthesis of biologically active compounds. J. Cossy, S. BouzBouz, F. Pradaux, C. Willis, V. Bellosta Synlett 2002, 1595.

[180] Enantioselective monoreduction of 2-alkyl-1,3-diketones mediated by chiral ruthenium catalysts. Dynamic kinetic resolution. F. Eustache, P. I. Dalko, J. Cossy Org. Lett. 2002, 4, 1263.

[179] Enantioselective Allyltitanations and Metathesis Reactions. Application to the synthesis of piperidine alkaloids (+)-sedamine and (-)-prosophylline. J. Cossy, C. Willis, V. Bellosta, S. BouzBouz J. Org. Chem. 2002, 67, 1982.

[178] Enantioselective allyltitanation. Synthesis of (-)-slaframine. J. Cossy, C. Willis, V. Bellosta, L. Saint-Jalmes Synthesis 2002, 951.

[177] Cross-metathesis reaction: direct synthesis of functionalized allylsilanes. S. BouzBouz, E. De Lemos, J. Cossy Adv. Synth. & Catal. 2002, 344, 627.

[176] Selective cyclopropylcarbinyl rearrangement of tricyclo[5.3.1.0]undecanols induced by pyridinium chlorochromate. J. Cossy, S. BouzBouz, M. Laghgar, B. Tabyaoui Tetrahedron Lett. 2002, 43, 823.

[175] Formal total synthesis of (+)-methynolide. J. Cossy, D. Bauer, V. Bellosta Synlett 2002, 715.

[174] Selective protection of spirocyclic diols. An unusual acetal opening by DIBAL-H. J. Cossy, B. Gille, V. Bellosta, A. Duprat New J. Chem. 2002, 26, 526.

[173] Modular ligands for asymmetric synthesis: enantioselective catalytic Cu(II)-mediated condensation reaction of ethyl pyruvate with Danishefsky’s diene. P. I. Dalko, L. Moisan, J. Cossy Angew. Chem., Int. Ed. 2002, 41, 625.

[172] Carbon-carbon bond forming reactions by using bistrifluoromethanesulfonimide. J. Cossy, F. Lutz, V. Alauze, C. Meyer Synlett 2002, 45.

2001

[171] A short formal synthesis of paroxetine. Diastereoselective cuprate addition to a chiral racemic olefinic amido ester. J. Cossy, O. Mirguet, D. Gomez Pardo, J. R. Desmurs Tetrahedron Lett. 2001, 42, 7805-7807.

[170] Cross-metathesis reaction. Generation of highly functionalized olefins from unsaturated alcohols. J. Cossy, S. BouzBouz, A. H. Hoveyda J. Organomet. Chem. 2001, 634, 216-221.

[169] The Iodocyclization of unsaturated dihydroxysulfonamide derivatives. N- versus O-cyclisation. J. Cossy, L. Tresnard, D. Belotti, D. Gomez Pardo Tetrahedron Lett. 2001, 42, 251-254.

[168] Synthesis of isopropenylcyclopropanes - revision of the relative configuration of cyclopropyl ketones obtained by 1,3-elimination of gamma-epoxy ketones. J. Cossy, N. Blanchard, C. Meyer Eur. J. Org. Chem. 2001, 2, 339-348.

[167] Cross-metathesis reaction. Generation of highly functionalized olefins from homoallylic alcohols. J. Cossy, S. BouzBouz J. Organomet. Chem. 2001, 327.

[166] Total Synthesis of (-)-4a,5-dihydrostreptazoline. J. Cossy, I. Pevet, C. Meyer Eur. J. Org. Chem, 2001, 2841-2850.

[165] Hydroxylation of olefins using molecular oxygen via alkylboronic esters. C. Cadot, P. I. Dalko, J. Cossy Tetrahedron Lett. 2001, 42, 1661-1663.

[164] Solid-support synthesis of 1,2-diols and g-lactones through addition of alpha-(benzyloxy)crotylindium reagents to aldehydes. J. Cossy, C. Rasamison, D. Gomez Pardo, J. A. Marshall Synlett 2001, 629-633.

[163] Diastereoselective synthesis of homopropargylic alcohols on solid support. J. Cossy, M. Defosseux, C. Meyer Synlett 2001, 815-817.

[162] Heterocyclisation of azacyanine with amines. Synthesis of new fused triazines and pyrimidine rings. M. T. Kaddachi, S. Zouari, H. Ben Ammar, J. Cossy, P. H. Kahn J. Soc. Chim. Tun. 2001, 4, 1171.

[161] Direct diastereoselective synthesis of (±)-cis and (±)-trans-4-methylpipecolic acid and derivatives. J. Cossy, D. Belotti Tetrahedron Lett. 2001, 42, 2119-2120.

[160] Efficient synthesis of substituted quinoline-5,8-quinones from 8-hydroxyquinolines by photooxygenation. J. Cossy, D. Belotti Tetrahedron Lett. 2001, 42, 4329-4331.

[159] Formal total synthesis of bisabolangelone by using a radical cyclization. J. Cossy, V. Bellosta, B. Gille Comptes Rendus de l’Académie des Sciences 2001, 4, 427-429.

[158] Formation of radicals by irradiation of alkyl halides in the presence of triethylamine. Application to the synthesis of (+)-bisabolangelone. J. Cossy, V. Bellosta, J. L. Ranaivosata, B. Gille Tetrahedron 2001, 57, 5173-5182.

[157] Composition and structural determination of the wax constituents of Jojoba oil extracted from the seeds od Simmondsia chinensis growing in Tunisia. M. T. Kaddachi, K. Mtibaa, M. Jouini, J. Cossy, P. H. Kahn J. Soc. Alg. Chim. 2001, 11, 143.

[156] Chemoselective cross-metathesis reaction. Application to the synthesis of the C1-C14 fragment of amphidinol 3. J. Cossy, S. BouzBouz Org. Lett. 2001, 3, 1451-1454.

[155] A Short Synthesis of Argatoban: a Potent Selective Thrombin Inhibitor. J. Cossy, D. Belotti Bio. Med. Chem. Lett. 2001, 11, 1989-1992.

[154] Reactivity of a-(benzoyloxy)crotylstannane with aldehydes in liquid phase and on solid support. Synthesis of substituted lactones. J. Cossy, C. Rasamison, D. Gomez Pardo J. Org. Chem. 2001, 66, 7195-7198.

[153] [2,3]-Wittig rearrangement of g-allyloxy-b-ketoesters. A new access to tetronic acids. I. Pevet, C. Meyer, J. Cossy Tetrahedron Lett. 2001, 42, 5215-5218.

[152] A short synthesis of cisapride: a gastrointestinal stimulant derived from cis-4-amino-3-methoxypiperidine. J. Cossy, J. L Molina, J. R. Desmurs Tetrahedron Lett. 2001, 42, 5713-5715.

[151] Synthesis of the C1-C12 fragment of fostriecin. J. Cossy, F. Pradaux, S. BouzBouz Org. Lett. 2001, 3, 2233-2235.

[150] Synthesis of stereotriads by oxymercuration of substitued cyclopropylcarbinols. J. Cossy, N. Blanchard, C. Meyer Org. Lett. 2001, 3, 2567-2569.

[149] Ruthenium-catalyzed asymmetric reduction of 1,3-diketones using transfer hydrogenation. J. Cossy, F. Eustache, P. Dalko Tetrahedron Lett. 2001, 42, 5005-5007.

[148] Ring expansion: Formal total synthesis of (-)-paroxetine. J. Cossy, O. Mirguet, D. Gomez Pardo, J. R. Desmurs Tetrahedron Lett. 2001, 42, 5705-5707.

[147] Efficient strategy for the synthesis of stereopentad subunits of scytophycin, discodermolide and ryfamycin S. S. BouzBouz, J. Cossy Org. Lett. 2001, 3, 3995-3998.

[146] Ring expansion. Synthesis of the velbanamine piperidine core. J. Cossy, O. Mirguet, D. Gomez Pardo Synlett 2001, 1575-1577.

[145] Enantioselective allyltitanation and cross-metathesis. Synthesis of (-)-prosophylline. J. Cossy, C. Willis, V. Bellosta Synlett 2001, 1578-1580.

2000

[144] A short and efficient synthesis of (-)-4a,5-dihydrostreptazolin. J. Cossy, I. Pevet, C. Meyer Synlett, 2000, 122-124.

[143] Enantioselective allyltitanation. Applications to the synthesis of lactone units related to compactin and mevinolin. J. Cossy, S. BouzBouz Tetrahedron Lett. 2000, 41, 3363-3366.

[142] Synthesis of amino alcohol derivatives from (L)-pyroglutamic acid on solid-phaset. J. Cossy, L. Tresnard, D. Gomez Pardo Synlett 2000, 409-411.

[141] Enantioselective synthesis of syn- and anti-1,3-diols via allyltitanation of unprotected β-hydroxy aldehydes. J. Cossy, S. BouzBouz Org. Lett. 2000, 2, 501-504.

[140] Organocopper reagents (RCu, R2CuLi) for the nucleophilic C-glycosylation of a C(2)-formyl glycal. J. Cossy, H. Rakotoarisoa Synlett 2000, 734-736.

[139] N-(2-acetoxyethyl) group as a new photolabile protecting group. J. Cossy, H. Rakotoarisoa Tetrahedron Lett. 2000, 41, 2097-2099.

[138] Metallic salts promoted radical cyclization of b-keto carboxamides and their correspnding β-enamino carboxamides. J. Cossy, A. Bouzide, C. Leblanc J. Org. Chem. 2000, 65, 7257-7265.

[137] Desymmetrization of meso aldehydes with optically active allytitanium complexes. J. Cossy, S. BouzBouz, M. Popkin Org. Lett. 2000, 2, 3449-3451.

[136] Radical carbon-carbon coupling reactions via organoboranes. C. Cadot, J. Cossy, P. Dalko J. Chem. Soc., Chem. Commun. 2000, 1017-1018.

[135] The use of TFSI-H in organic synthesis. J. Cossy, F. Lutz, V. Alauze, C. Meyer, J. R. Desmurs The Roots of Organic Development 2000, 9, 25.

[134] Troglitazone. A novel antidiabetic drug for treating insulin resistance. J. Cossy, C. Menciu, H. Rakatoarisoa, P. H. Kahn J. R. Desmurs The Roots of Organic Development 2000, 9, 9.

[133] Lewis acid-mediated nucleophilic reaction of 2-alkoxychromanes with silyl enol ethers. J. Cossy, H. Rakotoarisoa Tetrahedron Lett. 2000, 41, 7203-7205.

[132] Enantioselective allyltitanation. Efficient synthesis of the C1-C14 polyol subunit of amphotericine B. S. BouzBouz, J. Cossy Org. Lett, 2000, 2, 3975-3977.

[131] Enantioselective synthesis of propargylic alcohols by addition of enantiopure cyclopentadienyldialkoxyallyltitanium complexes to acetylenic aldehydes. F. Pradaux, S. Bouzbouz, J. Cossy, C. Ferroud, A. Falguieres Tetrahedron Lett. 2000, 41, 8877-8880.

[130] Enantioselective allyltitanation. Application to the synthesis of (+)-sedamine. J. Cossy, C. Willis, V. Bellosta, S. BouzBouz Synlett 2000, 1461-1463.

[129] The N-(2-acetoxyethyl) group as a new photolabile protecting group. J. Cossy, H. Rakotoarisoa Tetrahedron Lett. 2000, 41, 2097-2099.

1999

[128] A short synthesis of cordiachromene. P. H. Kahn, J. Cossy Tetrahedron Lett. 1999, 40, 8113-8114.

[127] A short synthesis of the C1-C7 fragment of methymycin by ring-closing olefin metathesis. J. Cossy, D. Bauer, V. Bellosta Tetrahedron Lett. 1999, 40, 4187-4188.

[126] A short synthesis of troglitazone: an antidiabetic drug for treating insulin resistance. J. Cossy, C. Menciu, H. Rakatoarisoa, P. H. Kahn, R.-R. Desmurs Bioorg. Med. Chem. Lett. 1999, 9, 3439-3440.

[125] Antiinflammatories. Synthesis of a nonsteroidal antiinflammatory ML 3000. J. Cossy Actualites de Chimie Therapeutique 1999, 25, 147-155.

[124] Approaches to a synthesis of α-kainic acid. J. Cossy, M. Cases, D. Gomez Pardo Tetrahedron 1999, 55, 6153-6166.

[123] Asymmetric synthesis: application to the synthesis of a platelet aggregation inhibitor and an M3 muscarinic receptor antagonist. J. Cossy Actualites de Chimie Therapeutique 1999, 25, 159-170.

[122] Derivatives of 7-Oxabicyclo[2.2.1]heptane in nature and as useful synthetic intermediates. P. Vogel, J. Cossy, J. Plumet, A. Odon Tetrahedron 1999, 55, 13521-13642.

[121] Diastereoselective hydroboration of Isopropenylcyclopropanes. J. Cossy, N. Blanchard, C. Hamel, C. Meyer J. Org. Chem. 1999, 64, 2608-2609.

[120] Diastereoselectivity in the dihydroxylation of isopropenyl substituted three-membered rings. J. Cossy, N. Blanchard, C. Meyer Tetrahedron Lett. 1999, 40, 8361-8364.

[119] Enantioselective allyltitanations. Synthesis of optically active 1,2-diol units: useful intermediates for the preparation of biologically active compounds. J. Cossy, S. Bouzbouz, J.-C. Caille Tetrahedron: Asymmetry 1999, 10, 3859-3862.

[118] Manganese(III) acetate and copper(II) acetate promoted oxidation of β-enamino amides and β-enamino esters. J. Cossy, A. Bouzide Tetrahedron 1999, 55, 6483-6496.

[117] Michael radical additions two short efficient syntheses of (+)-conocephalenol from (R)-pulegone. J. Cossy, S. Bouzbouz, A. Hakiki Tetrahedron 1999, 55, 11289-11294.

[116] Migratory insertion reactions of norbornene, norbornadiene and 7-oxanorbornene derivatives into the palladium-carbon bond of heterodinuclear Fe-Pd-Acyl complexes. Substrate influence on the Pd coordination sphere and crystal structure of cyclic (OC)3Feμ-Si(OMe)2(OMe)(μ-dppa)PdC9H9NO3COMe. P. Braunstein, J. Cossy, M. Knorr, C. Strohmann, P. Vogel New J. Chem. 1999, 23, 1215-1222.

[115] Oxidation of substituted spiro(bicyclo[n.1.0]alkane-2,2’-[1,3]dioxolanes). Formation of substituted lactones. J. Cossy, J.-L. Ranaivosata, B. Gille, V. Bellosta Tetrahedron 1999, 40, 4681-4682.

[114] Radical cyclizations. A convergent total synthesis of (±)-γ-lycorane. J. Cossy, L. Tresnard, D. Gomez Pardo Tetrahedron Lett. 1999, 40, 1125-1128.

[113] Radical cyclizations. Synthesis of γ-lycorane. J. Cossy, L. Tresnard, D. Gomez Pardo Eur. J. Org. Chem. 1999, 8, 1925-1933.

[112] Radical cyclizations. Synthesis of oxa- and azaheterocyclic compounds. J. Cossy Recent Res. Devel. Synth. Org. Chem. 1999, 2, 23-33.

[111] Reaction of functionalized ethoxyalkylidenes with 2-aminopyridine. Synthesis of 4-oxopyrido[1,2-a]pyrimidines and 4-iminopyrido[1,2-a]pyrimidines. M. T. Kaddachi, M. Ben Amor, S. Zouari, J. Cossy, P. H. Kahn J. Soc. Chim. Tunisie 1999, 4, 537-546.

[110] Ring expansion. Formation of optically active 3-hydroxypiperidines from pyrrolidinemethanol derivatives. J. Cossy, C. Dumas, D. Gomez Pardo Eur. J. Org. Chem. 1999, 1693-1699.

[109] Stereoselective synthesis of cyclopropanes bearing adjacent stereocenters. J. Cossy, N. Blanchard, C. Meyer Synthesis 1999, 1063-1075.

[108] Synthetic studies towards ML-3000. A concise synthesis of this non-steroidal antiinflammatory drug. J. Cossy, D. Belotti Tetrahedron 1999, 55, 5145-5156.

1998

[107] A convenient route to spiropyrrolidinyl-oxindole alkaloids via C-3 substituted ene-pyrrolidine carbamate radical cyclization. J. Cossy, M. Cases, D. Gomez Pardo Tetrahedron Lett. 1998, 39, 2331-2332.

[106] A formal synthesis of (-)-α-kainic acid. J. Cossy, M. Cases, D. Gomez Pardo Synlett 1998, 507-509.

[105]A one-pot synthesis of functionalized 2,2-disubstituted 2H-1-benzopyrans. J. Cossy, H. Rakotoarisoa, P. H. Kahn, J. R. Desmurs Tetrahedron Lett. 1998, 39, 9671-9674.

[104] A short total synthesis of (±)-isoafricanol and two of its isomers. J. Cossy, S. Bouzbouz, C. Mouza Synlett 1998, 621-622.

[103] A very simple method for converting Haworth representation to zigzag representation. J. Cossy, V. Bellosta J. Chem. Ed. 1998, 75, 1307.

[102] Directing effect of a neighboring aromatic group in the cyclopropanation of allylic alcohols. J. Cossy, N. Blanchard, C. Meyer J. Org. Chem. 1998, 63, 5728-5729.

[101] Facile synthesis of spirocyclic systems through the intramolecular addition of ketyl radicals via the sodium/ammonia reduction of δ,ε-unsaturated carboxylic esters. J. Cossy, B. Gille, V. Bellosta J. Org. Chem. 1998, 63, 3141-3146.

[100] Heck reaction versus free radical reaction for the synthesis of spiro(indoline-2,4’-piperidines). J. Cossy, C. Poitevin, D. Gomez Pardo, J. L. Peglion, A. Dessinges Synlett 1998, 251-252.

[99] Specific oxidative cleavage of allylic and benzylic ethers by using pyridinium chlorochromate. J. Cossy, S. Bouzbouz, M. Lachgar, A. Hakiki, B. Tabyaoui Tetrahedron Lett. 1998, 39, 2561-2564.

[98] Synthesis of Spiro(benzazepine-2,4‘-piperidine). J. Cossy, C. Poitevin, D. Gomez Pardo, J. L. Peglion, A. Dessinges J. Org. Chem. 1998, 63, 4554-4557.

[97] Synthesis of spiro(quinoline-2,4’-piperidines. J. Cossy, C. Poitevin, D. Gomez Pardo, J. L. Peglion, A. Dessinges Tetrahedron Lett. 1998, 39, 2965-2968.

[96] Synthesis of spirocyclic bislactones. Substituent effects on the regioselectivity of the Baeyer-Villiger oxidation of 1,3-diketones. J. Cossy, B. Gille, V. Bellosta Tetrahedron Lett. 1998, 39, 4459-4462.

1997

[95] 2-Methylcyclopentane-1,3-dione: an efficient synthon for the synthesis of (±)-α-cuparenone. J. Cossy, B. Gille, S. BouzBouz, V. Bellosta Tetrahedron Lett. 1997, 38, 4069-4070.

[94] A convenient procedure for the conversion of N-Boc protected pyrrolidinone derivatives into their corresponding enecarbamates. J. Cossy, M. Cases, D. Gomez Pardo Synthetic Commun. 1997, 27, 2769-2776.

[93] A short and efficient synthesis of zamifenacin a muscarinic M3 receptor antagonist. J. Cossy, C. Dumas, D. Gomez Pardo Bioorg. Med. Chem. Lett. 1997, 7, 1343-1344.

[92] A short enantioselective access to pumiliotoxin 251D from L-proline. J. Cossy, M. Cases,D. Gomez Pardo Bull. Soc. Chim. Fr. 1997, 134, 141-144.

[91] A thermal bicyclization. Synthesis of substituted 2,3,5,6-tetrahydro-6-oxo-1H-pyrrolizines. J. Cossy, D. Belotti Synlett 1997, 1249-1250.

[90] A very short and efficient synthesis of (+)-conocephalenol. J. Cossy, S. BouzBouz, A. Hakiki Tetrahedron Lett. 1997, 38, 8853-8854.

[89] A very short, efficient and inexpensive synthesis of the prodrug form of SC-54701A a platelet aggregation inhibitor. J. Cossy, A. Schmitt, C. Cinquin, D. Buisson, D. Belotti Bioorg. Med. Chem. Lett. 1997, 7, 1699-1700.

[88] An easy and efficient access to 2-bromo-4-methoxyaniline. J. Cossy, C. Poitevin, D. Gomez Pardo, J. L. Peglion Synthetic Commun. 1997, 27, 3525-3527.

[87] Cyclization of δ,ε-acetylenic amines and amino acids into cyclic enamines. A very efficient and simple access to polysubstituted pyrrolidines. J. Cossy, D. Belloti, V. Bellosta, C. Boggio Tetrahedron Lett. 1997, 38, 2677-2680.

[86] Intramolecular hene reactions. Stereo- and enantioselective synthesis of spirolactams through thermolysis of enaminocarboxamides. J. Cossy, A. Bouzide, M. Pfau J. Org. Chem. 1997, 62, 7106-7113.

[85] Photoselective bond cleavage of tricyclo[5.3.1.01,7]undecane derivatives. A facile entry to carbocyclic taxane [A,B] ring system. J. Cossy, S. BouzBouz Tetrahedron Lett 1997, 38, 1931-1932.

[84] Synthesis the (-)-pseudoconhydrine through ring enlargment of L-proline derivative. J. Cossy, C. Dumas, D. Gomez Pardo Synlett 1997, 905-906.

[83] Synthesis of ML-3000. an inhibitor of cyclooxygenase and 5-lipoxygenase. J. Cossy, D. Belotti J. Org. Chem. 1997, 62, 7900-7901.

[82] Synthesis of oxygenated heterocycles from cyclic allylsiloxanes using ring-closing olefin methathesis. C. Meyer, J. Cossy Tetrahedron Lett. 1997, 38, 7861-7864.

[81] Thermolysis of N-unsaturated alkyl-β-ketoamides. An easy access to spirolactams. J. Cossy, A. Bouzide Tetrahedron 1997, 53, 5775-5784.

1996

[80] A short access to (+)-ptilocaulin. J. Cossy, S. BouzBouz Tetrahedron Lett. 1996, 37, 5091-5094.

[79] A short enantioselective access to (-)-pumiliotoxin 251D from L-proline. J. Cossy, M. Cases, D. Gomez Pardo Synlett, 1996, 909-910.

[78] An easy access to substituted aminopyranones from L-pyroglutamic acid. J. Cossy, M. Cases, D. Gomez Pardo Tetrahedron Lett. 1996, 37, 8173-8174.

[77] Applications of photoinduced electron transfer processes to ketone aldehydes and ester derivatives in organic synthesis. J. Cossy, J. P. Pete Advances in Electron Transfer Chemistry 1996, 5, 141-195-.

[76] Carbon-carbon bond formation in carbohydrates by photoreductive cyclization reaction. J. Cossy, S. Ibhi J. Carbohydrate Res. 1996, 189-196.

[75] Selective synthesis of substituted benzylic alcohols from aromatic substrates included in β-cyclodextrin. J. Doussot, A. Guy, R. Garreau, A. Falguières, J. Cossy, C. Amsterdamsky Bull. Soc. Chim. Fr. 1996, 161-166.

[74] Total synthesis of (±)-isoavenaciolide and of (±)-ethisiolide from (±)-oxabicyclo[2.2.1]hept-5-en-2-one. J. Cossy, J. L. Ranaivosata, V. Bellosta Tetrahedron 1996, 52, 629-638.

[73] The thermal rearrangement of N-alkyl-N-vinyl propargylamine into 2-methylpyrrole. A new synthesis of annulated[b]pyrroles. J. Cossy, C. Poitevin, L. Salle, D. Gomez Pardo Tetrahedron Lett. 1996, 37, 6709-6710.

1995

[72] A formal synthesis of ptaquilosin. The aglycon of a potent bracken carcinogen ptaquiloside. J. Cossy, S. Ibhi, P. H. Kahn, L. Tacchini Tetrahedron Lett. 1995, 36, 7877-7880.

[71] A selective and efficient demesylation using methylmagnesium bromide. J. Cossy, J.-L. Ranaivosata, V. Bellosta, R. Wietzke Synthetic Communications 1995, 25, 3109-3112.

[70] An approach to the skeleton of eriolanin. J. Cossy, J.-L. Ranaivosata, V. Bellosta Tetrahedron Lett. 1995, 36, 2067-2070.

[69] Electrochemical evidence for intramolecular reactions of the electrogenerated cation-radicals of some amidoenamines. P. Audebert, H. Bekolo, J. Cossy, A. Bouzide J. Electroanalytical. Chem. 1995, 389, 215-218.

[68] Formation of optically active 3-hydroxypiperidines. J. Cossy, C. Dumas, P. Michel, D. Gomez Pardo Tetrahedron Lett. 1995, 36, 549-552.

[67] N-Bromosuccinimide mediated ring-opening of cyclopropylcarbinols. J. Cossy, N. Furet Tetrahedron Lett. 1995, 36, 3691-3694.

[66] Reactivity of tris(trimethylsilyl)silyl radical with β-alkenyloxyenones. J. Cossy, L. Salle Tetrahedron Lett. 1995, 36, 7235-7238.

[65] Reductive Oxa Ring Opening of 7-Oxabicyclo[2.2.1]heptan-2-ones. Synthesis of C-α-Galactosides of Carbapentopyranoses. J. Cossy, J.-L. Ranaivosata, V. Bellosta, J. Ancerewicz, R. Ferritto, P. Vogel J. Org. Chem. 1995, 60, 8351-8359.

[64] Ring opening of cyclopropyl ketones induced by photochemical electron transfer. J. Cossy, N. Furet, S. BouzBouz Tetrahedron 1995, 51, 11751-11764.

[63] Synthesis of 2-(alkylamino)benzonitriles from α-(bromoarylamino)nitriles. J. Cossy, C. Poitevin, D. Gomez Pardo, J.-L. Peglion Synthesis 1995, 1368-1370.

1994

[62] A very useful and mild method for the protection and deprotection of carboxylic acids. J. Cossy, A. Albouy, M. Scheloske, D. Gomez Pardo Tetrahedron Lett. 1994, 35, 1539-1540.

[61] Diels-Alder reaction. P. Vogel, A. Guy, Y. Langlois, A. Lubineau, D. Grierson, R. Bloch, J. Cossy Actualite Chimique 1994, 7, 21-28

[60] Formation of radicals by irradiation of alkyl halides in the presence of triethylamine. J. Cossy, J.-L. Ranaivosata, V. Bellosta Tetrahedron Lett. 1994, 35, 8161-8162.

[59] Intramolecular quenching of iminium ions generated by photooxidation of aminoalcohols with ketones. A new synthesis of oxazines and oxazoles. J. Cossy, M. Guha Tetrahedron Lett. 1994, 35, 1715-1718.

[58] Oxidative cleavage of 2-substituted cycloalkane-1,3-diones and of cyclic β-keto esters by copper perchlorate/oxygen. J. Cossy, D. Belotti, V. Bellosta, D. Brocca Tetrahedron Lett. 1994, 35, 6089-6092.

[57] Photochemical access to alkyl 3-deoxyglycopyranosid-4-uloses. J. Cossy, S. Ibhi Carbohydrate Research 1994, 259, 141-146.

[56] Photochemical electron transfer reactions. Applications to organic synthesis. J. Cossy Bull. Soc. Chim. Fr. 1994, 131, 344-356.

[55] Photoreduction of α-keto amides; cyclization of unsaturated captodative radicals. J. Cossy, A. Madaci, J.-P. Pete Tetrahedron Lett. 1994, 35, 1541-1544.

[54] Short and efficient access to β-keto amides. J. Cossy, D. Belotti, A. Bouzide, A. Thellend Bull. Soc. Chim. Fr. 1994, 131, 723-729.

[53] Total synthesis of ethisolide from "naked sugars". J. Cossy, J.-L. Ranaivosata, V. Bellosta Tetrahedron Lett. 1994, 35, 1205-1208.

1993

[52] Dehydrogenation of carboxamidoenamines with manganese acetate and copper acetate. J. Cossy, A. Bouzide Tetrahedron Lett. 1993, 34, 5583-5562.

[51] Generation of radical cations from enamines and their addition to unactivated olefins. J. Cossy, A. Bouzide J. Chem. Soc., Chem. Commun. 1993, 15, 1218-1219.

[50] Hydroxylated indolizidines and their synthesis. J. Cossy, P. Vogel Studies in Natural Products Chemistry 1993, 12, 275-363.

[49] N-(Phenylseleno)phthalimide: A useful reagent for the α-selenylation of ketones and aldehydes. J. Cossy, N. Furet Tetrahedron Lett. 1993, 34, 7755-7756.

[48] Photochemical ring opening of cyclopropyl ketones induced by electron transfer. J. Cossy, N. Furet Tetrahedron Lett. 1993, 34, 8107-8110.

[47] Photoreductive cyclization of N,N-dialkyl-β-oxoamides: synthesis of piperidines and δ-lactams. J. Cossy, D. Belotti, N. K. Cuong, C. Chassagnard Tetrahedron 1993, 49, 7691-7700.

[46] Radical cyclization of N-alkyl-N-unsaturated alkyl-β-carboxamidoenamines induced by manganese acetate. J. Cossy, A. Bouzide, C. Leblanc Synlett 1993, 3, 202-204.

[45] Total synthesis of (±)-actinidine and of (±)-isooxyskytanthine. J. Cossy, D. Belotti, C. Leblanc J. Org. Chem. 1993, 58, 2351-2354.

1992

[44] Asymmetric intramolecular ene-reaction. J. Cossy, A. Bouzide, M. Pfau Tetrahedron Lett. 1992, 33, 4883-4884.

[43] Conformational analysis of α-methoxy ketones. A photoelectron spectroscopic investigation of 3-methoxybicyclo[2.2.1]heptan-2-ones. J. Cossy, J.-P. Pete, R. Gleiter, A. Flatow, P.-A. Carrupt, P. Vogel Tetrahedron 1992, 48, 2401-2414.

[42] Regio- and stereoselective cyclizations. Application to natural products synthesis. J. Cossy Pure and Applied Chemistry 1992, 64, 1883-1888.

[41] Stereoselective formation of spiro lactams by intramolecular ene reaction. J. Cossy, A. Bouzide Tetrahedron Lett. 1992, 33, 2505-2508.

[40] Unusual reactivity of borane towards tetrahydropyranyl ethers. J. Cossy, V. Bellosta, M. C. Muller Tetrahedron Lett. 1992, 33, 5045-5046.

1991

[39] First efficient synthesis of isooxyskytanthine. J. Cossy, C. Leblanc Tetrahedron Lett. 1991, 32, 3051-3052.

[38] Formation of β-hydroxyketones from α,β-epoxyketones by photoinduced single electron transfer reactions. J. Cossy, A. Bouzide, S. Ibhi, P. Aclinou Tetrahedron 1991, 47, 7775-7782.

[37] Radical anion ring opening reactions via photochemically induced electron transfer. J. Cossy, P. Aclinou, V. Bellosta, N. Furet, J. Baranne-Lafont, D. Sparfel, C. Souchaud Tetrahedron Lett. 1991, 32, 1315-1316.

1990

[36] A one-step synthesis of functionalized lactams and spirolactams from unsaturated β-keto amides. J. Cossy, A.Thellend Tetrahedron Lett. 1990, 31, 1427-1428.

[35] Isolation and total synthesis of the major constituent of the roots of Centaurea incana:aplotaxene. J. Cossy, P. Aclinou Tetrahedron Lett. 1990, 31, 7615-7618.

[34] Total synthesis of (±)-hirsutene. J. Cossy, D. Belotti, J.-P. Pete Tetrahedron 1990, 46,1859-1870.

1989

[33] A 4-dimethylaminopyridine-catalyzed aminolysis of β-keto esters. Formation of β-keto amides. J. Cossy, A. Thellend Synlett 1989, 753-755.

[32] A short access to iridoid precursors. J. Cossy Tetrahedron Lett. 1989, 30, 4113-4116.

[31] A convenient synthesis of amides from carboxylic acids and primary amines. J. Cossy, C. Pale-Grosdemange Tetrahedron Lett. 1989, 30, 2771-2774.

[30] New synthesis of lactams and spirolactams. Radical cyclization induced by manganese(III) acetate. J. Cossy, C. Leblanc Tetrahedron Lett. 1989, 30, 4531-4534.

[29] Photoreductive cyclization of unsaturated aldehydes: an easy access to spiranic molecules. J. Cossy, J.-P. Pete, C. Portella Tetrahedron Lett. 1989, 30, 7361-7364.

[28] Stereochemistry of methyl 5-hydroxy-4-methylbicyclo[3.3.0]octanecarboxylates and of ethyl 5-hydroxy-4-methylbicyclo[4.3.0]nonanecarboxylates. J. Cossy, J. Bouquant, G. Dauphin, D. Belotti Bull. Soc. Chim. Fr. 1989, 879-883.

[27] Synthesis of a furofuranic model of natural antifeeding substances. A. P. Brunetiere, M. Leclaire, S. Bhatnagar, J.-Y. Lallemand, J. Cossy Tetrahedron Lett. 1989, 30, 341-344.

1988

[26] A very simple synthesis of α-substituted β-keto amides. J. Cossy, D. Belotti, A. Thellend, J. P. Pete Synthesis 1988, 720-1

[25] Photoreductive cyclization. Application to the total synthesis of (±)-actinidine. J. Cossy, D. Belotti, J.-P. Pete Tetrahedron Lett. 1988, 29, 6113-6114.

[24] Synthesis of medium-ring lactones: Application to the synthesis of 15-pentadecanolide and phoracantholide I. J. Cossy, J.-P. Pete Bull. Soc. Chim. Fr. 1988, 6, 989-994.

1987

[23] A simple and convenient method for the cleavage of dithio acetals to the corresponding carbonyl compounds. J. Cossy Synlett 1987, 1113-1115.

[22] A very short access to 4-substituted thiochromans. J. Cossy, F. Henin, C. Leblanc Tetrahedron Lett. 1987, 28, 1417-1418.

[21] Methyleneindolines, indolenines, and indoleniniums. XXII. A biomimetic entry into the hexacyclic tuboxenin ring system. G. Hugel, J. Cossy, J. Levy Tetrahedron Lett. 1987, 28, 1773-1776.

[20] Photoreductive cyclization of N,N-dialkyl-β-oxo amides: formation of six-membered ring lactams. J. Cossy, D. Belotti, J.-P. Pete Tetrahedron Lett. 1987, 28, 4545-4546.

[19] Photoreductive cyclization: Application to the total synthesis of (±)-hirsutene. J. Cossy, D. Belotti, J.-P. Pete Tetrahedron Lett. 1987, 28, 4547-4550.

[18] Selective silylation by hexamethyldisilazane. J. Cossy, J.-P. Pete Tetrahedron Lett. 1987, 28, 6039-6040.

1986

[17] A one step synthesis of ω-hydroxyacetylenic carboxylic acids. J. Cossy, J.-P. Pete Tetrahedron Lett. 1986, 27, 573-574.

[16] A three-step synthesis of exaltolide and phoracantholide I. J. Cossy, J.-P. Pete Tetrahedron Lett. 1986, 27, 2369-2370.

[15] Synthesis of bicyclic cyclopentanols by photoreductive cyclization of δ,ε-unsaturated ketones. D. Belotti, J. Cossy, J.-P. Pete, C. Portella, C. J. Org. Chem. 1986, 51, 4196-4200.

1985

[14] Palladium-catalyzed oxidation of allylsilanes with UV light and molecular oxygen. A. Riahi, J. Cossy, J. Muzart, J.-P. Pete Tetrahedron Lett. 1985, 26, 839-842.

[13] Photoreductive cyclization of δ,ε-unsaturated ketones. D. Belotti, J. Cossy, J.-P. Pete, C. Portella Tetrahedron Lett. 1985, 26, 4591-4594.

1984

[12] 3-Tolyl-2-isopropylamino-2-cyclohexenone. J. Cossy J. Photochem. 1984, 27, 115-116.

[11] A simple apparatus for filtering air-sensitive solids. J. Cossy, A. Feigenbaum J. Chem. Ed. 1984, 61, 453.

[10] The photochemical cyclization of 2-alkylamino-3-aryl-2-cyclohexenones. J. Cossy, J.-P. Pete Heterocycles 1984, 22, 97-100.

1983

[9] 1,1-Bis(benzenesulfonyl)cyclopropane: A synthon for a propylene 1,3-dipole. B. M. Trost, J. Cossy, J. Burks J. Am. Chem. Soc. 1983, 105, 1052-1054.

1982

[8] Palladium-mediated macroheterocyclization. A synthesis of inandenin-12-one. B. M. Trost, J. Cossy J. Am. Chem. Soc. 1982, 104, 6881-6882.

1981

[7] Photochemical reactivity of 2-dialkylamino-2-cyclohexenones and the corresponding ammonium salts. J. C. Arnould, J. Cossy, J.-P. Pete Tetrahedron 1981, 37, 1921-1926.

[6] Study of the mechanism of the photochemical transformation of 2-alkyl-2-arenesulfonamido-2-cyclohexenones to 2-alkylamino-3-aryl-2-cyclohexenones. J. Cossy, J.-P. Pete Tetrahedron 1981, 37, 2287-2296.

1980

[5] Photochemical reactivity of α-aminoenones: cyclization and new type of reaction to α-sulfonamidocyclohexenones. J. C. Arnould, J. Cossy, J.-P. Pete Tetrahedron 1980, 36, 1585-1592.

[4] Photochemical reactivity of 2-alkylamino 2-cyclohexenones. Formation of ketoaziridines. J. Cossy, J.-P. Pete Tetrahedron Lett. 1980, 21, 2947-2948.

1979

[3] Synthesis and photochemical reactivity of ethyl 3-(alkylamino)-3-(2-pyridyl)propanoates and -propenoates. J. Cossy, J.-P. Pete Bull. Soc. Chim. Fr. 1979, 9-10, Pt. 2, 559-567.

1978

[2] Photodehydrogenation of substituted pyrrolidines. Hydrogen transfer induced by benzophenone. J. Cossy, J.-P. Pete Tetrahedron Lett. 1978, 19, 4941-4944.

1976

[1] Photolysis of 2(N-alkyl-arylsulfonylamido) cyclohexenone. An unusual and useful desulfonation reaction. J. C. Arnould, J. Cossy, J.-P. Pete Tetrahedron Lett. 1976, 17, 3919-3922.

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The CMC team is part of the Molecular, Macromolecular Chemistry and Materials research unit (C3M, UMR7167) along with the CDM and CPF teams (former MMC lab).

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