| Year |
Citation |
Score |
| 2021 |
Cossy J, Leverenz M, Masson G, Pardo DG. Synthesis of Azocanes from Piperidines via an Azetidinium Intermediate. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34643301 DOI: 10.1002/chem.202102739 |
0.73 |
|
| 2017 |
Rioton S, Pardo DG, Cossy J. Synthesis of Substituted α-Trifluoromethyl Piperidinic Derivatives. Molecules (Basel, Switzerland). 22. PMID 28335499 DOI: 10.3390/Molecules22030483 |
0.527 |
|
| 2014 |
Orliac A, Routier J, Charvillon FB, Sauer WH, Bombrun A, Kulkarni SS, Pardo DG, Cossy J. Enantioselective synthesis and physicochemical properties of libraries of 3-amino- and 3-amidofluoropiperidines. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 3813-24. PMID 24532344 DOI: 10.1002/Chem.201302423 |
0.43 |
|
| 2014 |
Duthion B, Pardo DG, Cossy J. Synthesis of LY503430 by using a selective rearrangement of β-amino alcohols induced by DAST Arkivoc. 2014: 239-255. DOI: 10.3998/Ark.5550190.P008.252 |
0.534 |
|
| 2014 |
Anxionnat B, Pardo DG, Ricci G, Rossen K, Cossy J. Correction to Iridium-Catalyzed Hydrogen Transfer: Synthesis of Substituted Benzofurans, Benzothiophenes, and Indoles from Benzyl Alcohols Organic Letters. 16: 2297-2297. DOI: 10.1021/Ol500762N |
0.57 |
|
| 2014 |
Anxionnat B, Pardo DG, Ricci G, Cossy J. Correction to Monoalkylation of Acetonitrile by Primary Alcohols Catalyzed by Iridium Complexes Organic Letters. 16: 2296-2296. DOI: 10.1021/Ol403135H |
0.482 |
|
| 2012 |
Cochi A, Pardo DG, Cossy J. Synthesis of two neurokinin NK1 receptor antagonists: (+)-L-733,060 and (-)-L-733,061 Heterocycles. 86: 89-116. DOI: 10.3987/Rev-12-Sr(N)2 |
0.443 |
|
| 2012 |
Anxionnat B, Pardo DG, Ricci G, Cossy J. First Intramolecular Alkylation of Nitriles with Primary and Secondary Alcohols Catalyzed by Iridium Complexes: Intramolecular Alkylation of Nitriles Catalyzed by Iridium Complexes European Journal of Organic Chemistry. 2012: 4453-4456. DOI: 10.1002/Ejoc.201200850 |
0.531 |
|
| 2012 |
Cochi A, Pardo DG, Cossy J. Access to optically active 3-aminopiperidines by ring expansion of prolinols: Thermodynamic versus kinetic control European Journal of Organic Chemistry. 2023-2040. DOI: 10.1002/Ejoc.201101829 |
0.528 |
|
| 2011 |
Cochi A, Pardo DG, Cossy J. Access to optically active 3-azido- and 3-aminopiperidine derivatives by enantioselective ring expansion of prolinols. Organic Letters. 13: 4442-5. PMID 21793544 DOI: 10.1021/Ol201769B |
0.557 |
|
| 2011 |
Anxionnat B, Pardo DG, Ricci G, Cossy J. Monoalkylation of acetonitrile by primary alcohols catalyzed by iridium complexes. Organic Letters. 13: 4084-7. PMID 21732660 DOI: 10.1021/Ol2015972 |
0.524 |
|
| 2010 |
Cochi A, Métro TX, Pardo DG, Cossy J. Enantioselective synthesis of SSR 241586 by using an organo-catalyzed Henry reaction. Organic Letters. 12: 3693-5. PMID 20666443 DOI: 10.1021/Ol101555G |
0.548 |
|
| 2010 |
Ferret H, Déchamps I, Pardo DG, Hijfte LV, Cossy aJ. Ring enlargement and ring contraction induced by DAST Arkivoc. 2010. DOI: 10.3998/Ark.5550190.0011.812 |
0.36 |
|
| 2010 |
Pardo D, Cossy J, Duthion B. Synthesis of LY503430 Synfacts. 2011: 0013-0013. DOI: 10.1055/S-0030-1258979 |
0.54 |
|
| 2010 |
Ferret H, Déchamps I, Pardo DG, Van Hijfte L, Cossy J. Ring enlargement and ring contraction induced by Diethylaminosulfur trifluoride (DAST) Arkivoc. 2010: 126-159. |
0.448 |
|
| 2009 |
Cossy J, Pardo DG, Dumas C, Mirguet O, Déchamps I, Métro TX, Burger B, Roudeau R, Appenzeller J, Cochi A. Rearrangement of beta-amino alcohols and application to the synthesis of biologically active compounds. Chirality. 21: 850-6. PMID 19408325 DOI: 10.1002/Chir.20716 |
0.516 |
|
| 2009 |
Lacheretz R, Pardo DG, Cossy J. Daucus carota mediated-reduction of cyclic 3-oxo-amines. Organic Letters. 11: 1245-8. PMID 19215083 DOI: 10.1021/Ol8029214 |
0.566 |
|
| 2009 |
Cochi A, Burger B, Navarro C, Pardo DG, Cossy J, Zhao Y, Cohen T. Enantioselective ring expansion of prolinols: An efficient and short synthesis of 2-phenylpiperidin-3-ol derivatives and 3-hydroxypipecolic acids Synlett. 2157-2161. DOI: 10.1055/S-0029-1217568 |
0.61 |
|
| 2009 |
Lacheretz R, Pardo DG, Cossy J. Reducing Ketones with Carrots Synfacts. 2009: 555-555. DOI: 10.1055/S-0029-1216574 |
0.466 |
|
| 2008 |
Métro TX, Pardo DG, Cossy J. Syntheses of (S,S)-reboxetine via a catalytic stereospecific rearrangement of beta-amino alcohols. The Journal of Organic Chemistry. 73: 707-10. PMID 18092801 DOI: 10.1021/Jo701554H |
0.518 |
|
| 2008 |
Métro T-, Pardo DG, Cossy J. Synthesis of (S,S)-Reboxetine Synfacts. 2008: 559-559. DOI: 10.1055/S-2008-1072611 |
0.408 |
|
| 2007 |
Métro TX, Pardo DG, Cossy J. Highly enantioselective synthesis of beta-amino alcohols: a catalytic version. The Journal of Organic Chemistry. 72: 6556-61. PMID 17658853 DOI: 10.1021/Jo071028X |
0.529 |
|
| 2007 |
Métro TX, Pardo DG, Cossy J. Stereospecific rearrangement of β-amino alcohols catalyzed by H 2SO4 Synlett. 2888-2890. DOI: 10.1055/S-2007-992351 |
0.506 |
|
| 2007 |
Déchamps I, Pardo DG, Cossy J. Synthesis of optically active substituted 3-fluoropiperidines from prolinols by using dast Synlett. 2007: 263-267. DOI: 10.1055/S-2007-967989 |
0.469 |
|
| 2007 |
Déchamps I, Pardo DG, Cossy J. Enantioselective ring expansion of prolinol derivatives. Two formal syntheses of (-)-swainsonine Tetrahedron. 63: 9082-9091. DOI: 10.1016/J.Tet.2007.06.086 |
0.59 |
|
| 2007 |
Déchamps I, Pardo DG, Cossy J. Ring expansion induced by DAST: Synthesis of substituted 3-fluoropiperidines from prolinols and 3-fluoroazepanes from 2-hydroxymethylpiperidines European Journal of Organic Chemistry. 4224-4234. DOI: 10.1002/Ejoc.200700237 |
0.576 |
|
| 2006 |
Métro TX, Appenzeller J, Pardo DG, Cossy J. Highly enantioselective synthesis of β-amino alcohols Organic Letters. 8: 3509-3512. PMID 16869647 DOI: 10.1021/Ol061133D |
0.538 |
|
| 2006 |
Déchamps I, Pardo DG, Cossy J. Enantioselective ring expansion of prolinols and ring-closing metathesis: formal synthesis of (−)-swainsonine Arkivoc. 2007. DOI: 10.3998/Ark.5550190.0008.504 |
0.617 |
|
| 2006 |
Cossy J, Cases M, Pardo DG. A Convenient Procedure for the Conversion Of N-Boc Protected Pyrrolidinone Derivatives Into Their Corresponding Enecarbamates Synthetic Communications. 27: 2769-2776. DOI: 10.1080/00397919708004150 |
0.418 |
|
| 2005 |
Filippis A, Pardo D, Cossy J. A Very Short and Efficient Synthesis of Preclamol Letters in Organic Chemistry. 2: 136-138. DOI: 10.2174/1570178053202883 |
0.544 |
|
| 2005 |
Déchamps I, Pardo DG, Karoyan P, Cossy J. Efficient enantioselective formal synthesis of Ro 67-8867, a NMDA 2B receptor antagonist Synlett. 2005: 1170-1172. DOI: 10.1055/S-2005-865225 |
0.598 |
|
| 2004 |
Cossy J, Pardo DG. Enantioselective Ring Expansion via Aziridinium Intermediates: Synthesis of Substituted Piperidines from Substituted Pyrrolidines — Synthetic Applications Cheminform. 35. DOI: 10.1002/chin.200429273 |
0.589 |
|
| 2003 |
Cossy J, De Filippis A, Pardo DG. Palladium-catalyzed intermolecular alpha-arylation of N-protected 2-piperidinones. Organic Letters. 5: 3037-9. PMID 12916975 DOI: 10.1021/Ol0350036 |
0.503 |
|
| 2003 |
Cossy J, Mirguet O, Pardo DG, Desmurs J. Diastereoselective conjugate addition of organocuprates to chiral racemic olefinic amido esters. Formal total synthesis of paroxetine New Journal of Chemistry. 27: 475-482. DOI: 10.1039/B209181J |
0.611 |
|
| 2002 |
Cossy J, Rasamison C, Pardo DG. Reactivity of alpha-(benzoyloxy)crotylstannane with aldehydes in liquid phase and on solid support. Synthesis of substituted lactones. The Journal of Organic Chemistry. 66: 7195-8. PMID 11597251 DOI: 10.1021/Jo010152S |
0.493 |
|
| 2002 |
Cossy J, Mirguet O, Pardo D, Desmurs J. A Formal Synthesis of (−)-Paroxetine by Enantioselective Ring Enlargement of a Trisubstituted Prolinol European Journal of Organic Chemistry. 2002: 3543-3551. DOI: 10.1002/1099-0690(200211)2002:21<3543::Aid-Ejoc3543>3.0.Co;2-0 |
0.596 |
|
| 2001 |
Cossy J, Mirguet O, Pardo DG. Ring Expansion: Synthesis of the Velbanamine Piperidine Core Synlett. 2001: 1575-1577. DOI: 10.1055/S-2001-17454 |
0.578 |
|
| 2001 |
Cossy J, Rasamison C, Pardo DG, Marshall JA. Solid-Support Synthesis of 1,2-Diols and γ-Lactones Through Addition of α-(Benzoyloxy)crotylindium Reagents to Aldehydes Synlett. 2001: 0629-0633. DOI: 10.1055/s-2001-13367 |
0.496 |
|
| 2001 |
Cossy J, Rasamison C, Pardo DG, Marshall JA. Solid-support synthesis of 1,2-diols and γ-lactones through addition of α-(benzoyloxy)crotylindium reagents to aldehydes Synlett. 629-633. DOI: 10.1055/S-2001-13367 |
0.551 |
|
| 2001 |
Cossy J, Mirguet O, Pardo DG, Desmurs J. Ring expansion: formal total synthesis of (−)-paroxetine Tetrahedron Letters. 42: 5705-5707. DOI: 10.1016/S0040-4039(01)01096-6 |
0.586 |
|
| 2000 |
Cossy J, Tresnard L, Pardo DG. Synthesis of Amino Alcohol Derivatives from (l)-Pyroglutamic Acid on Solid-Phase Synlett. 2000: 409-411. DOI: 10.1055/S-2000-6516 |
0.54 |
|
| 1999 |
Cossy J, Tresnard L, Pardo DG. Radical cyclizations. A convergent total synthesis of (±)-γ-lycorane Tetrahedron Letters. 40: 1125-1128. DOI: 10.1016/S0040-4039(98)02585-4 |
0.547 |
|
| 1999 |
Cossy J, Tresnard L, Pardo DG. Radical Cyclizations – Synthesis of γ-Lycorane European Journal of Organic Chemistry. 1999: 1925-1933. DOI: 10.1002/(Sici)1099-0690(199908)1999:8<1925::Aid-Ejoc1925>3.0.Co;2-# |
0.612 |
|
| 1999 |
Cossy J, Dumas C, Pardo DG. Ring Expansion – Formation of Optically Active 3-Hydroxypiperidines from Pyrrolidinemethanol Derivatives European Journal of Organic Chemistry. 1999: 1693-1699. DOI: 10.1002/(Sici)1099-0690(199907)1999:7<1693::Aid-Ejoc1693>3.0.Co;2-J |
0.494 |
|
| 1998 |
Cossy J, Poitevin C, Pardo DG. Heck Reaction versus Free Radical Reaction for the Synthesis of Spiro[indoline-2,4′-piperidines] Synlett. 9: 251-252. DOI: 10.1055/S-1998-1622 |
0.519 |
|
| 1998 |
Cossy J, and CP, Pardo DG, and J-P, Dessinges A. Synthesis of Spiro[benzazepine-2,4‘-piperidine] Journal of Organic Chemistry. 63: 4554-4557. DOI: 10.1021/Jo9803986 |
0.56 |
|
| 1998 |
Cossy J, Poitevin C, Pardo DG, Peglion J, Dessinges A. Synthesis of spiro[quinoline-2,4′-piperidines] Heck versus radical reaction Tetrahedron Letters. 39: 2965-2968. DOI: 10.1016/S0040-4039(98)00389-X |
0.58 |
|
| 1998 |
Cossy J, Cases M, Pardo DG. A convenient route to spiropyrrolidinyl-oxindole alkaloids via C-3 substituted ene-pyrrolidine carbamate radical cyclization Tetrahedron Letters. 39: 2331-2332. DOI: 10.1016/S0040-4039(98)00193-2 |
0.588 |
|
| 1997 |
Cossy J, Poitevin C, Pardo DG, Peglion JL. An Easy and Efficient Access to 2-Bromo-4-methoxyaniline Synthetic Communications. 27: 3525-3527. DOI: 10.1080/00397919708007073 |
0.408 |
|
| 1997 |
Cossy J, Dumas C, Pardo DG. Synthesis of (-)-Pseudoconhydrine through Ring Enlargement of a L-Proline Derivative Synlett. 1997: 905-906. DOI: 10.1055/S-1997-5789 |
0.568 |
|
| 1997 |
Cossy J, Dumas C, Pardo DG. A Short And Efficient Synthesis Of Zamifenacin A Muscarinic M3 Receptor Antagonist Bioorganic & Medicinal Chemistry Letters. 7: 1343-1344. DOI: 10.1016/S0960-894X(97)00221-7 |
0.555 |
|
| 1996 |
Cossy J, Cases M, Pardo DG. A Short Enantioselective Access to Pumiliotoxin 251D from L-Proline Synlett. 1996: 909-910. DOI: 10.1055/S-1996-5590 |
0.438 |
|
| 1996 |
Cossy J, Poitevin C, Sallé L, Pardo DG. The thermal rearrangement of N-alkyl-N-vinylpropargylamines into 2-methylpyrroles. A new synthesis of annulated[b]pyrroles Tetrahedron Letters. 37: 6709-6710. DOI: 10.1016/S0040-4039(96)01467-0 |
0.465 |
|
| 1996 |
Cossy J, Cases M, Pardo DG. An easy access to substituted aminopyranones from L-pyroglutamic acid Tetrahedron Letters. 37: 8173-8174. DOI: 10.1016/0040-4039(96)01863-1 |
0.557 |
|
| 1995 |
Cossy J, Poitevin C, Pardo DG, Peglion JL. Synthesis of 2-(Alkylamino)benzonitriles from α-(Bromoarylamino)nitriles Synthesis. 1995: 1368-1370. DOI: 10.1055/S-1995-4126 |
0.531 |
|
| 1995 |
Cossy J, Dumas C, Michel P, Pardo DG. Formation of optically active 3-hydroxypiperidines Tetrahedron Letters. 36: 549-552. DOI: 10.1016/0040-4039(94)02338-C |
0.539 |
|
| 1994 |
Cossy J, Albouy A, Scheloske M, Pardo DG. A very useful and mild method for the protection and deprotection of carboxylic acids Tetrahedron Letters. 35: 1539-1540. DOI: 10.1016/S0040-4039(00)76752-9 |
0.467 |
|
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