| Year |
Citation |
Score |
| 2016 |
Quinodoz P, Wright K, Drouillat B, David O, Marrot J, Couty F. Synthesis of homopropargylamines from 2-cyanoazetidines. Chemical Communications (Cambridge, England). PMID 27457376 DOI: 10.1039/c6cc05713f |
0.394 |
|
| 2016 |
Quinodoz P, Drouillat B, Wright K, Marrot J, Couty F. N-Arylazetidines: Preparation through Anionic Ring Closure. The Journal of Organic Chemistry. 81: 2899-910. PMID 26932242 DOI: 10.1021/acs.joc.6b00169 |
0.385 |
|
| 2016 |
Barbier V, Couty F, David OR. Furan-2,3-diones as masked dipoles: synthesis of isotetronic acids and mechanistic considerations Tetrahedron. 72: 5646-5651. DOI: 10.1016/J.TET.2016.07.072 |
0.312 |
|
| 2016 |
Barbier V, Couty F, David ORP. ChemInform Abstract: Furan-2,3-diones as Masked Dipoles: Synthesis of Isotetronic Acids and Mechanistic Considerations. Cheminform. 47. DOI: 10.1002/CHIN.201651113 |
0.337 |
|
| 2016 |
Quinodoz P, Wright K, Drouillat B, David O, Marrot J, Couty F. ChemInform Abstract: Synthesis of Homopropargylamines from 2-Cyanoazetidines. Cheminform. 47. DOI: 10.1002/CHIN.201650049 |
0.399 |
|
| 2015 |
Drouillat B, Wright K, Quinodoz P, Marrot J, Couty F. Aza-[2,3]-Wittig Sigmatropic Rearrangement of Allylic Tertiary Amines: A Successful Example with High Chirality Transfer. The Journal of Organic Chemistry. 80: 6936-40. PMID 26036310 DOI: 10.1021/acs.joc.5b01230 |
0.308 |
|
| 2014 |
Laouiti A, Couty F, Marrot J, Boubaker T, Rammah MM, Rammah MB, Evano G. Exploring the anionic reactivity of ynimines, useful precursors of metalated ketenimines. Organic Letters. 16: 2252-5. PMID 24702158 DOI: 10.1021/ol500749h |
0.503 |
|
| 2013 |
Gati W, Couty F, Boubaker T, Rammah MM, Rammah MB, Evano G. Intramolecular carbocupration of N-aryl-ynamides: a modular indole synthesis. Organic Letters. 15: 3122-5. PMID 23734901 DOI: 10.1021/ol4013298 |
0.679 |
|
| 2013 |
Couty F, Drouillat B, Evano G, David O. 2-cyanoazetidines and azetidinium ions: Scaffolds for molecular diversity European Journal of Organic Chemistry. 2045-2056. DOI: 10.1002/Ejoc.201201685 |
0.619 |
|
| 2013 |
Couty F, Drouillat B, Evano G, David O. ChemInform Abstract: 2-Cyanoazetidines and Azetidinium Ions: Scaffolds for Molecular Diversity Cheminform. 44: no-no. DOI: 10.1002/CHIN.201332216 |
0.474 |
|
| 2012 |
Gati W, Rammah MM, Rammah MB, Couty F, Evano G. De novo synthesis of 1,4-dihydropyridines and pyridines. Journal of the American Chemical Society. 134: 9078-81. PMID 22583001 DOI: 10.1021/ja303002a |
0.631 |
|
| 2012 |
Laouiti A, Rammah MM, Rammah MB, Marrot J, Couty F, Evano G. Copper-catalyzed oxidative alkynylation of diaryl imines with terminal alkynes: a facile synthesis of ynimines. Organic Letters. 14: 6-9. PMID 22171540 DOI: 10.1021/ol2032152 |
0.597 |
|
| 2011 |
De Rycke N, Berionni G, Couty F, Mayr H, Goumont R, David OR. Synthesis and reactivity of highly nucleophilic pyridines. Organic Letters. 13: 530-3. PMID 21186828 DOI: 10.1021/Ol1029589 |
0.349 |
|
| 2011 |
Evano G, Tadiparthi K, Couty F. Copper-mediated cross-coupling of 1,1-dibromo-1-alkenes with dialkyl phosphites: a convenient synthesis of 1-alkenylphosphonates. Chemical Communications (Cambridge, England). 47: 179-81. PMID 20625578 DOI: 10.1039/c0cc01617a |
0.579 |
|
| 2010 |
Jouvin K, Couty F, Evano G. Copper-catalyzed alkynylation of amides with potassium alkynyltrifluoroborates: a room-temperature, base-free synthesis of ynamides. Organic Letters. 12: 3272-5. PMID 20565123 DOI: 10.1021/ol101322k |
0.588 |
|
| 2010 |
Chopin N, Couty F, Evano G. Synthesis of the Azetidinyl-Thiazoline Fragment of Vioprolides A and C Letters in Organic Chemistry. 7: 353-359. DOI: 10.2174/157017810791514814 |
0.55 |
|
| 2010 |
Evano G, Coste A, Couty F. Copper-Mediated Homocoupling of Vinyl Dibromides to Symmetrical Diynes Synthesis. 2010: 1500-1504. DOI: 10.1055/S-0029-1218688 |
0.507 |
|
| 2010 |
De Rycke N, Marrot J, Couty F, David OR. Synthesis and characterization of hexasubstituted azacryptands Tetrahedron Letters. 51: 6521-6525. DOI: 10.1016/J.TETLET.2010.10.019 |
0.377 |
|
| 2010 |
Chopin N, Couty F, Evano G. ChemInform Abstract: Synthesis of the Azetidinyl-Thiazoline Fragment of Vioprolides A and C. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201047187 |
0.566 |
|
| 2010 |
Coste A, Couty F, Evano G. ChemInform Abstract: Copper-Mediated Homocoupling of Vinyl Dibromides to Symmetrical Diynes. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201035057 |
0.529 |
|
| 2010 |
Couty F, Evano G. ChemInform Abstract: Azetidines: New Tools for the Synthesis of Nitrogen Heterocycles Cheminform. 41. DOI: 10.1002/CHIN.201012231 |
0.619 |
|
| 2010 |
Coste A, Couty F, Evano G. ChemInform Abstract: Synthesis of Ketene N,N-Acetals by Copper-Catalyzed Double-Amidation of 1,1-Dibromo-1-alkenes. Cheminform. 41. DOI: 10.1002/CHIN.201008046 |
0.632 |
|
| 2010 |
Agami C, Couty F, Rabasso N. ChemInform Abstract: An Efficient Asymmetric Synthesis of Azetidine 2-Phosphonic Acids. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200240115 |
0.345 |
|
| 2010 |
Agami C, Couty F, Evano G. ChemInform Abstract: A Straightforward Synthesis of Enantiopure 2-Cyano Azetidines from β-Amino Alcohols. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200234122 |
0.559 |
|
| 2010 |
Agami C, Couty F, Evano G. ChemInform Abstract: Claisen Rearrangements of Allylic and Propargylic Alcohols Prepared by an N-Boc-2-acyloxazolidine Methodology - Application to the Synthesis of Original Chiral Building Blocks. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200224131 |
0.626 |
|
| 2010 |
Agami C, Couty F, Rabasso N. ChemInform Abstract: N-Boc-2-acyl Oxazolidine Methodology Combined with Ring-Closing Metathesis: A New Approach Towards the Enantioselective Synthesis of α-(1-Hydroxyalkyl) Nitrogen Heterocycles. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200143135 |
0.393 |
|
| 2010 |
Agami C, Couty F, Rabasso N. ChemInform Abstract: Synthesis of (-)-β Conhydrine and Analogues Using N-Boc-2-acyl Oxazolidine Methodology and Ring Closing Metathesis. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200036225 |
0.373 |
|
| 2010 |
Agami C, Couty F, Evano G, Mathieu H. ChemInform Abstract: SN2′ Regio- and Stereoselective Alkylation of Allylic and Propargylic Mesylates Linked to an N-Boc Oxazolidine Using Organocuprates. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200019112 |
0.628 |
|
| 2010 |
Agami C, Couty F, Mathieu H, Pilot C. ChemInform Abstract: SN2′ Regio- and Stereoselective Alkylation of Allylic Mesylates Linked to a N-Boc Oxazolidine Using Organocuprates. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199935031 |
0.371 |
|
| 2010 |
Agami C, Couty F, Evano G. ChemInform Abstract: Selective N-Dealkylation of Tertiary Amines Derived from Phenylglycinol or Ephedrine Family. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199931081 |
0.546 |
|
| 2010 |
AGAMI C, COUTY F, LAM H, MATHIEU H. ChemInform Abstract: A New Access to Enantiopure β-Hydroxylated Piperidines from N-Boc-2-acyloxazolidines. Application to the Synthesis of (-)-Desoxoprosopinine and (+)-Pseudoconhydrine. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199844232 |
0.335 |
|
| 2010 |
AGAMI C, AMIOT F, COUTY F, DECHOUX L. ChemInform Abstract: Synthesis of Enantiopure Substituted Aziridines by Diastereoselective N-Bromocyclization and Nucleophile-Mediated Regioselective Opening. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199843144 |
0.466 |
|
| 2010 |
AGAMI C, COUTY F, PUCHOT-KADOURI C. ChemInform Abstract: Asymmetric Synthesis of α-Amino Acids from a Chiral Masked Form of Glyoxal Cheminform. 29: no-no. DOI: 10.1002/CHIN.199834311 |
0.302 |
|
| 2010 |
AGAMI C, COUTY F, MATHIEU H. ChemInform Abstract: Total Synthesis of (-)-Desoxoprosopinine via the Diastereoselective Reduction of Homochiral 2-Acyl-N-Boc-oxazolidines. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199832272 |
0.424 |
|
| 2010 |
KRIEF A, COUTY F. ChemInform Abstract: Synthesis of 1-Aryl-2-vinyl Cyclopropanes by Intramolecular Carbolithiation. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199807108 |
0.444 |
|
| 2010 |
AGAMI C, COUTY F, MATHIEU H. ChemInform Abstract: Cyclization of a Chiral Oxazolidine as a Key Step for the Synthesis of Functionalized Piperidines. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199639164 |
0.398 |
|
| 2010 |
AGAMI A, COUTY F, VENIER O. ChemInform Abstract: A Highly Diastereoselective Epoxidation of N-Boc 2-Alkenyloxazolidines: Application in Asymmetric Synthesis. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199611171 |
0.426 |
|
| 2010 |
AGAMI C, COUTY F, LEQUESNE C. ChemInform Abstract: N-Boc-2-acyloxazolidines: Useful Precursors to Enantiopure 1,2-Diols via Highly Diastereoselective Nucleophilic Additions. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199534033 |
0.346 |
|
| 2010 |
AGAMI C, CASES M, COUTY F. ChemInform Abstract: A New Access to Kainoids via a Tandem Aza-Cope/Mannich Reaction. Application to the Enantioselective Synthesis of (-)-α- Allokainic Acid. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199526212 |
0.349 |
|
| 2010 |
AGAMI C, COUTY F, LEQUESNE C. ChemInform Abstract: Asymmetric Synthesis of Homochiral 1,2-Diols via N-Boc Oxazolidines. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199438040 |
0.422 |
|
| 2010 |
AGAMI C, COUTY F, LIN J, MIKAELOFF A. ChemInform Abstract: Aza-Cope/Mannich Tandem Reaction Applied to the Asymmetric Synthesis of a Homochiral Proline Derivative. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199408175 |
0.382 |
|
| 2010 |
AGAMI C, COUTY F, LIN J, MIKAELOFF A, POURSOULIS M. ChemInform Abstract: Asymmetric Synthesis of α-Amino Acids via Cationic Aza-Cope Rearrangements. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199350286 |
0.3 |
|
| 2010 |
AGAMI C, COUTY F, HAMON L, VENIER O. ChemInform Abstract: Chiral Oxazolidinones from N-Boc Derivatives of β-Amino Alcohols. Effect of a N-Methyl Substituent on Reactivity and Stereoselectivity. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199340200 |
0.315 |
|
| 2010 |
AGAMI C, COUTY F, POURSOULIS M, VAISSERMANN J. ChemInform Abstract: Asymmetric Synthesis of Pipecolic Acid Derivatives. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199219280 |
0.358 |
|
| 2010 |
AGAMI C, COUTY F, PRINCE B, PUCHOT C. ChemInform Abstract: Asymmetric Synthesis of N-Methyl-α-amino Esters from a Glyoxal Derived Chiral Heterocycle. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199137243 |
0.382 |
|
| 2010 |
AGAMI C, COUTY F. ChemInform Abstract: Enantioselective Synthesis of Pipecolic Acid Derivatives via an Ene- Iminium Cyclization. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199120176 |
0.395 |
|
| 2009 |
Coste A, Couty F, Evano G. Synthesis of ketene N,N-acetals by copper-catalyzed double-amidation of 1,1-dibromo-1-alkenes. Organic Letters. 11: 4454-7. PMID 19775187 DOI: 10.1021/ol901831s |
0.631 |
|
| 2009 |
Coste A, Karthikeyan G, Couty F, Evano G. Copper-mediated coupling of 1,1-dibromo-1-alkenes with nitrogen nucleophiles: a general method for the synthesis of ynamides. Angewandte Chemie (International Ed. in English). 48: 4381-5. PMID 19441026 DOI: 10.1002/anie.200901099 |
0.611 |
|
| 2009 |
Couty F, Evano G. Azetidines: New Tools for the Synthesis of Nitrogen Heterocycles Synlett. 2009: 3053-3064. DOI: 10.1055/S-0029-1218299 |
0.609 |
|
| 2009 |
David O, Couty F. Synthesis of an Ovoid Chiral Cage Synlett. 2009: 1945-1948. DOI: 10.1055/S-0029-1217523 |
0.368 |
|
| 2009 |
Evano G, Coste A, Karthikeyan G, Couty F. Second-Generation, Biomimetic Total Synthesis of Chaetominine Synthesis. 2009: 2927-2934. DOI: 10.1055/S-0029-1216923 |
0.602 |
|
| 2009 |
Toumi M, Rincheval V, Young A, Gergeres D, Turos E, Couty F, Mignotte B, Evano G. A General Route to Cyclopeptide Alkaloids: Total Syntheses and Biological Evaluation of Paliurines E and F, Ziziphines N and Q, Abyssenine A, Mucronine E, and Analogues European Journal of Organic Chemistry. 2009: 3368-3386. DOI: 10.1002/Ejoc.200900122 |
0.562 |
|
| 2009 |
Toumi M, Couty F, Marrot J, Evano G. ChemInform Abstract: Total Synthesis of Chaetominine (VII). Cheminform. 40. DOI: 10.1002/CHIN.200912199 |
0.636 |
|
| 2008 |
Toumi M, Couty F, Marrot J, Evano G. Total synthesis of chaetominine. Organic Letters. 10: 5027-30. PMID 18847212 DOI: 10.1021/ol802155n |
0.625 |
|
| 2008 |
Coste A, Toumi M, Wright K, Razafimahaléo V, Couty F, Marrot J, Evano G. Copper-catalyzed cyclization of iodo-tryptophans: a straightforward synthesis of pyrroloindoles. Organic Letters. 10: 3841-4. PMID 18681449 DOI: 10.1021/ol8015513 |
0.623 |
|
| 2008 |
Toumi M, Couty F, Evano G. Total synthesis of the cyclopeptide alkaloid paliurine E. insights into macrocyclization by ene--enamide RCM. The Journal of Organic Chemistry. 73: 1270-81. PMID 18205380 DOI: 10.1021/jo702092x |
0.641 |
|
| 2008 |
Couty F, Drouillat B, David O, Evano G, Marrot J. Rearrangement of 2-Hydroxyalkylazetidines into 3-Fluoropyrrolidines Synlett. 2008: 1345-1348. DOI: 10.1055/S-2008-1072770 |
0.542 |
|
| 2008 |
Evano G, Toumi M, Couty F. Eight-Step Total Synthesis of the Cyclopeptide Alkaloid Mucronine E Synlett. 2008: 29-32. DOI: 10.1055/S-2007-1000833 |
0.58 |
|
| 2008 |
Toumi M, Couty F, Evano G. A practical route to enantiopure 3-hydroxy-pyrrolidines: application to a straightforward synthesis of (−)-bulgecinine Tetrahedron Letters. 49: 1175-1179. DOI: 10.1016/J.TETLET.2007.12.051 |
0.584 |
|
| 2008 |
Coste A, Couty F, Evano G. TMC-95A–D and analogues: Chemistry and biology Comptes Rendus Chimie. 11: 1544-1573. DOI: 10.1016/J.CRCI.2008.06.003 |
0.53 |
|
| 2008 |
Durrat F, Sanchez MV, Couty F, Evano G, Marrot J. Ring Expansion of 2‐(α‐Hydroxyalkyl)azetidines: A Synthetic Route to Functionalized Pyrrolidines European Journal of Organic Chemistry. 2008: 3286-3297. DOI: 10.1002/EJOC.200800316 |
0.553 |
|
| 2008 |
Durrat F, Vargas Sanchez M, Couty F, Evano G, Marrot J. ChemInform Abstract: Ring Expansion of 2-(α-Hydroxyalkyl)azetidines: A Synthetic Route to Functionalized Pyrrolidines. Cheminform. 39. DOI: 10.1002/CHIN.200844117 |
0.557 |
|
| 2008 |
Drouillat B, Couty F, David O, Evano G, Marrot J. ChemInform Abstract: Rearrangement of 2-Hydroxyalkylazetidines into 3-Fluoropyrrolidines. Cheminform. 39. DOI: 10.1002/CHIN.200840103 |
0.546 |
|
| 2008 |
Toumi M, Couty F, Evano G. ChemInform Abstract: A Practical Route to Enantiopure 3-Hydroxy-pyrrolidines: Application to a Straightforward Synthesis of (-)-Bulgecinine (XVI). Cheminform. 39. DOI: 10.1002/CHIN.200824103 |
0.607 |
|
| 2008 |
Toumi M, Couty F, Evano G. ChemInform Abstract: Eight-Step Total Synthesis of the Cyclopeptide Alkaloid Mucronine E. Cheminform. 39. DOI: 10.1002/CHIN.200821188 |
0.592 |
|
| 2007 |
Toumi M, Couty F, Evano G. Total synthesis of the cyclopeptide alkaloid abyssenine A. Application of inter- and intramolecular copper-mediated coupling reactions in organic synthesis. The Journal of Organic Chemistry. 72: 9003-9. PMID 17508763 DOI: 10.1021/jo070517u |
0.622 |
|
| 2007 |
Toumi M, Couty F, Evano G. Total synthesis of paliurine F. Angewandte Chemie (International Ed. in English). 46: 572-5. PMID 17036293 DOI: 10.1002/anie.200602865 |
0.527 |
|
| 2007 |
Couty F, David O, Durrat F. Chemo- and regioselective reductive opening of azetidinium ions Tetrahedron Letters. 48: 1027-1031. DOI: 10.1016/J.Tetlet.2006.11.175 |
0.318 |
|
| 2007 |
Sivaprakasam M, Couty F, David O, Marrot J, Sridhar R, Srinivas B, Rao KR. A straightforward synthesis of enantiopure bicyclic azetidines European Journal of Organic Chemistry. 2007: 5734-5739. DOI: 10.1002/Ejoc.200700616 |
0.411 |
|
| 2007 |
Couty F, Durrat F, Evano G. Ring Expansion and Ring Opening of Azetidines Cheminform. 38. DOI: 10.1002/CHIN.200704235 |
0.514 |
|
| 2007 |
Toumi M, Couty F, Evano G. Cover Picture: Total Synthesis of Paliurine F (Angew. Chem. Int. Ed. 4/2007) Angewandte Chemie International Edition. 46: 475-475. DOI: 10.1002/ANIE.200790000 |
0.526 |
|
| 2007 |
Toumi M, Couty F, Evano G. Titelbild: Total Synthesis of Paliurine F (Angew. Chem. 4/2007) Angewandte Chemie. 119: 479-479. DOI: 10.1002/ANGE.200790000 |
0.527 |
|
| 2006 |
Vargas-Sanchez M, Lakhdar S, Couty F, Evano G. Reaction of azetidines with chloroformates. Organic Letters. 8: 5501-4. PMID 17107057 DOI: 10.1021/Ol062128C |
0.548 |
|
| 2006 |
Sivaprakasham M, Couty F, Evano G, Srinivas B, Sridhar R, Rao KR. A straightforward synthesis of 3-substituted azetidinic amino acids Arkivoc. 2007: 71-93. DOI: 10.3998/ARK.5550190.0008.A08 |
0.585 |
|
| 2006 |
Couty F, Evano G. AZETIDINE-2-CARBOXYLIC ACID. FROM LILY OF THE VALLEY TO KEY PHARMACEUTICALS. A JUBILEE REVIEW Organic Preparations and Procedures International. 38: 427-465. DOI: 10.1080/00304940609356436 |
0.488 |
|
| 2006 |
Couty F, Evano G, Menguy L, Steimetz V, Toumi M. N-Cyanomethyl-β-chloro amines: chiral building blocks for the synthesis of azacrown ethers Tetrahedron Letters. 47: 4817-4821. DOI: 10.1016/J.TETLET.2006.05.046 |
0.615 |
|
| 2006 |
Couty F, Durrat F, Evano G, Marrot J. Ring Expansions of 2-Alkenylazetidinium Salts – a New Route to Pyrrolidines and Azepanes European Journal of Organic Chemistry. 2006: 4214-4223. DOI: 10.1002/EJOC.200600362 |
0.556 |
|
| 2006 |
Couty F, David O, Durrat F, Evano G, Lakhdar S, Marrot J, Vargas-Sanchez M. Nucleophilic ring-opening of azetidinium ions: Insights into regioselectivity European Journal of Organic Chemistry. 3479-3490. DOI: 10.1002/Ejoc.200600200 |
0.548 |
|
| 2006 |
Couty F, Evano G. Azetidine-2-carboxylic Acid. From Lily of the Valley to Key Pharmaceuticals Cheminform. 37. DOI: 10.1002/CHIN.200652239 |
0.502 |
|
| 2006 |
Couty F, Durrat F, Evano G, Marrot J. Ring Expansions of 2-Alkenylazetidinium Salts — A New Route to Pyrrolidines and Azepanes. Cheminform. 37. DOI: 10.1002/CHIN.200652115 |
0.555 |
|
| 2006 |
Sivaprakasam M, Couty F, Evano G, Srinivas B, Sridhar R, Rao KR. Stereocontrolled Synthesis of 3-Substituted Azetidinic Amino Acids. Cheminform. 37. DOI: 10.1002/CHIN.200629087 |
0.585 |
|
| 2005 |
Vargas-Sanchez M, Couty F, Evano G, Prim D, Marrot J. 3-Aminopyrrolidines via ring rearrangement of 2-aminomethylazetidines. Synthesis of (-)-absouline. Organic Letters. 7: 5861-4. PMID 16354085 DOI: 10.1021/ol052388e |
0.63 |
|
| 2005 |
Bräuner-Osborne H, Bunch L, Chopin N, Couty F, Evano G, Jensen AA, Kusk M, Nielsen B, Rabasso N. Azetidinic amino acids: stereocontrolled synthesis and pharmacological characterization as ligands for glutamate receptors and transporters. Organic & Biomolecular Chemistry. 3: 3926-36. PMID 16240010 DOI: 10.1039/B509514J |
0.552 |
|
| 2005 |
Couty F, Evano G, Vargas-Sanchez M, Bouzas G. Practical asymmetric preparation of azetidine-2-carboxylic acid. The Journal of Organic Chemistry. 70: 9028-31. PMID 16238345 DOI: 10.1021/jo0515881 |
0.611 |
|
| 2005 |
Couty F, Evano G, Prim D. N-Cyanomethyl-β-chloroamines: a convenient source of aziridinium ions Tetrahedron Letters. 46: 2253-2257. DOI: 10.1016/J.TETLET.2005.02.016 |
0.501 |
|
| 2005 |
Keller L, Sanchez MV, Prim D, Couty F, Evano G, Marrot J. Azetidines as ligands in the Pd(II) complexes series Journal of Organometallic Chemistry. 690: 2306-2311. DOI: 10.1016/J.JORGANCHEM.2005.02.041 |
0.434 |
|
| 2005 |
Couty F, Durrat F, Evano G. Regioselective Nucleophilic Opening of Azetidinium Ions. Cheminform. 36. DOI: 10.1002/CHIN.200546036 |
0.489 |
|
| 2005 |
Couty F, Evano G, Prim D. N-Cyanomethyl-β-chloroamines: A Convenient Source of Aziridinium Ions. Cheminform. 36. DOI: 10.1002/CHIN.200529085 |
0.501 |
|
| 2005 |
Couty F, Durrat F, Evano G, Prim D. Synthesis and Reactivity of Enantiomerically Pure N-Alkyl-2-alkenyl Azetidinium Salts. Cheminform. 36. DOI: 10.1002/CHIN.200503109 |
0.659 |
|
| 2004 |
Couty F, Evano G, Prim D. Synthesis of Chiral Non Racemic Azetidines Mini-Reviews in Organic Chemistry. 1: 133-148. DOI: 10.2174/1570193043488845 |
0.606 |
|
| 2004 |
Couty F, Durrat F, Evano G, Prim D. Synthesis and reactivity of enantiomerically pure N-alkyl-2-alkenyl azetidinium salts Tetrahedron Letters. 45: 7525-7528. DOI: 10.1016/J.TETLET.2004.07.113 |
0.659 |
|
| 2004 |
Couty F, Evano G, Prim D, Marrot J. General Route to a New Class of Homochiral Azetidine-Derived 1,2-Diamines European Journal of Organic Chemistry. 2004: 3893-3897. DOI: 10.1002/EJOC.200400233 |
0.52 |
|
| 2004 |
Agami C, Couty F. The Use of
N
‐Boc‐1,3‐Oxazolidines as Chiral Auxiliaries in Asymmetric Synthesis European Journal of Organic Chemistry. 2004: 677-685. DOI: 10.1002/EJOC.200300452 |
0.383 |
|
| 2004 |
Couty F, Evano G, Prim D, Marrot J. General Route to a New Class of Homochiral Azetidine-Derived 1,2-Diamines. Cheminform. 35. DOI: 10.1002/CHIN.200451086 |
0.52 |
|
| 2004 |
Couty F, Evano G, Prim D. Synthesis of Chiral Non-Racemic Azetidines Cheminform. 35. DOI: 10.1002/CHIN.200432282 |
0.606 |
|
| 2004 |
Agami C, Couty F. The Use of N-Boc-1,3-Oxazolidines as Chiral Auxiliaries in Asymmetric Synthesis Cheminform. 35. DOI: 10.1002/CHIN.200424219 |
0.388 |
|
| 2003 |
Couty F, Evano G, Rabasso N. Synthesis of enantiopure azetidine 2-carboxylic acids and their incorporation into peptides Tetrahedron: Asymmetry. 14: 2407-2412. DOI: 10.1016/S0957-4166(03)00493-2 |
0.54 |
|
| 2003 |
Agami C, Couty F, Evano G, Darro F, Kiss R. Enantioselective Synthesis of Clavepictine Analogues and Evaluation of Their Cytotoxic Activity European Journal of Organic Chemistry. 2003: 2062-2070. DOI: 10.1002/EJOC.200300057 |
0.575 |
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| 2003 |
Carlin-Sinclair A, Couty F, Rabasso N. Asymmetric Synthesis of Functionalized Azetidines Through Intramolecular Michael Additions. Cheminform. 34. DOI: 10.1002/CHIN.200331110 |
0.37 |
|
| 2003 |
Couty F, Prim D. Synthesis of Enantiopure 2-Acyl Azetidines and the Application of Amino Alcohols Derived Therefrom in Enantioselective Catalysis. Cheminform. 34. DOI: 10.1002/CHIN.200315044 |
0.307 |
|
| 2002 |
Couty F, Prim D. Synthesis of enantiopure 2-acyl azetidines and the application of amino alcohols derived therefrom in enantioselective catalysis Tetrahedron: Asymmetry. 13: 2619-2624. DOI: 10.1016/S0957-4166(02)00710-3 |
0.307 |
|
| 2002 |
Agami C, Couty F, Evano G. A straightforward synthesis of enantiopure 2-cyano azetidines from β-amino alcohols Tetrahedron: Asymmetry. 13: 297-302. DOI: 10.1016/S0957-4166(02)00076-9 |
0.548 |
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| 2002 |
Agami C, Couty F, Rabasso N. An efficient asymmetric synthesis of azetidine 2-phosphonic acids Tetrahedron Letters. 43: 4633-4636. DOI: 10.1016/S0040-4039(02)00868-7 |
0.319 |
|
| 2002 |
Agami C, Couty F, Evano G. Claisen Rearrangements of Allylic and Propargylic Alcohols Prepared by an N-Boc-2-acyloxazolidine Methodology − Application to the Synthesis of Original Chiral Building Blocks European Journal of Organic Chemistry. 2002: 29-38. DOI: 10.1002/1099-0690(20021)2002:1<29::AID-EJOC29>3.0.CO;2-B |
0.622 |
|
| 2001 |
Agami C, Couty F, Rabasso N. N -Boc-2-acyl oxazolidine methodology combined with ring-closing metathesis: a new approach towards the enantioselective synthesis of α-(1-hydroxyalkyl) nitrogen heterocycles Tetrahedron. 57: 5393-5401. DOI: 10.1016/S0040-4020(01)00458-6 |
0.383 |
|
| 2001 |
Agami C, Couty F, Evano G. ChemInform Abstract: Enantioselective Synthesis of 2-Substituted-N-Boc-Δ-4,5-piperidines. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200119124 |
0.674 |
|
| 2001 |
Agami C, Couty F, Evano G. ChemInform Abstract: Claisen Rearrangement of Allylic Alcohols Prepared Through N-Boc-2-acyloxazolidine Methodology. Application to the Synthesis of Trisubstituted Cyclopropanes. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200103116 |
0.621 |
|
| 2000 |
Agami C, Couty F, Evano G. Enantioselective synthesis of 2-substituted-N-Boc-Δ-4,5-piperidines Tetrahedron: Asymmetry. 11: 4639-4643. DOI: 10.1016/S0957-4166(00)00462-6 |
0.668 |
|
| 2000 |
Agami C, Couty F, Evano G. Claisen rearrangement of allylic alcohols prepared through N-Boc-2-acyloxazolidine methodology. Application to the synthesis of trisubstituted cyclopropanes Tetrahedron Letters. 41: 8301-8305. DOI: 10.1016/S0040-4039(00)01465-9 |
0.612 |
|
| 2000 |
Agami C, Couty F, Rabasso N. Synthesis of (−)-β conhydrine and analogues using N-Boc-2-acyl oxazolidine methodology and ring closing metathesis Tetrahedron Letters. 41: 4113-4116. DOI: 10.1016/S0040-4039(00)00580-3 |
0.361 |
|
| 2000 |
Agami C, Couty F, Evano G, Mathieu H. SN2′ Regio and Stereoselective Alkylation of Allylic and Propargylic Mesylates Linked to a N-Boc Oxazolidine using Organocuprates Tetrahedron. 56: 367-376. DOI: 10.1016/S0040-4020(99)00949-7 |
0.617 |
|
| 2000 |
Agami C, Couty F, Evano G. ChemInform Abstract: Synthesis of α-Substituted Allylic Amines via a Modified Bruylants Reaction. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200045075 |
0.619 |
|
| 1999 |
Agami C, Couty F, Mathieu H, Pilot C. SN2′ regio and stereoselective alkylation of allylic mesylates linked to a N-Boc oxazolidine using organocuprates Tetrahedron Letters. 40: 4539-4542. DOI: 10.1016/S0040-4039(99)00800-X |
0.351 |
|
| 1999 |
Agami C, Couty F, Evano G. Selective N-dealkylation of tertiary amines derived from phenylglycinol or ephedrine family Tetrahedron Letters. 40: 3709-3712. DOI: 10.1016/S0040-4039(99)00594-8 |
0.531 |
|
| 1998 |
Agami C, Amiot F, Couty F, Dechoux L. Synthesis of enantiopure substituted aziridines by diastereoselective N-bromocyclization and nucleophile-mediated regioselective opening Tetrahedron Letters. 39: 5373-5374. DOI: 10.1016/S0040-4039(98)01109-5 |
0.453 |
|
| 1998 |
Agami C, Couty F, Mathieu H. Total synthesis of (−)-desoxoprosopinine via the diastereoselective reduction of homochiral2-Acyl-N-Boc-oxazolidines Tetrahedron Letters. 39: 3505-3508. DOI: 10.1016/S0040-4039(98)00646-7 |
0.371 |
|
| 1998 |
Agami C, Couty F, Lam H, Mathieu H. A new access to enantiopure β-hydroxylated piperidines from N-Boc-2-acyloxazolidines. Application to the synthesis of (−)-desoxoprosopinine and (+)-pseudoconhydrine Tetrahedron. 54: 8783-8796. DOI: 10.1016/S0040-4020(98)00508-0 |
0.321 |
|
| 1997 |
Agami C, Couty F, Hamon L, Venier O. Regio- and Stereocontrolled Formation of Chiral Epoxy Oxazolidines via Bromocarbamation of N-Boc Alkenyl Oxazolidines. Application to Asymmetric Synthesis. The Journal of Organic Chemistry. 62: 2106-2112. PMID 11671515 DOI: 10.1021/jo962277g |
0.773 |
|
| 1997 |
Krief A, Couty F. Synthesis of 1-Aryl-2-Vinyl Cyclopropanes by Intramolecular Carbolithiation Tetrahedron Letters. 38: 8085-8088. DOI: 10.1016/S0040-4039(97)10115-0 |
0.441 |
|
| 1996 |
Agami C, Couty F, Mathieu H. Cyclization of a chiral oxazolidine as a key-step for the synthesis of functionalized piperidines Tetrahedron Letters. 37: 4001-4002. DOI: 10.1016/0040-4039(96)00767-8 |
0.387 |
|
| 1995 |
Agami A, Couty F, Venier O. A Highly Diastereoselective Epoxidation of N-Boc 2-Alkenyloxazolidines: Application in Asymmetric Synthesis Synlett. 1995: 1027-1028. DOI: 10.1055/S-1995-5159 |
0.408 |
|
| 1995 |
Agami C, Couty F, Lequesne C. N-Boc 2-Acyloxazolidines: Useful precursors to enantiopure 1,2-diols via highly diastereoselective nucleophilic additions Tetrahedron. 51: 4043-4056. DOI: 10.1016/0040-4020(95)00145-X |
0.324 |
|
| 1994 |
Agami C, Cases M, Couty F. A New Access to Kainoids via a Tandem Aza-Cope/Mannich Reaction. Application to the Enantioselective Synthesis of (-)-.alpha.-Allokainic Acid The Journal of Organic Chemistry. 59: 7937-7940. DOI: 10.1021/JO00104A066 |
0.3 |
|
| 1994 |
Agami C, Couty F, Lequesne C. Asymmetric synthesis of homochiral 1,2-diols via N-boc oxazolidines Tetrahedron Letters. 35: 3309-3312. DOI: 10.1016/S0040-4039(00)76893-6 |
0.404 |
|
| 1993 |
Agami C, Couty F, Lin J, Mikaeloff A. Aza-Cope/Mannich Tandem Reaction Applied to the Asymmetric Synthesis of a Homochiral Proline Derivative Synlett. 1993: 349-350. DOI: 10.1055/S-1993-22451 |
0.364 |
|
| 1993 |
Agami C, Couty F, Hamon L, Venier O. Chiral oxazolidinones from N-Boc derivatives of β-amino alcohols. Effect of a N-methyl substituent on reactivity and stereoselectivity Tetrahedron Letters. 34: 4509-4512. DOI: 10.1016/0040-4039(93)88071-P |
0.304 |
|
| 1992 |
Agami C, Couty F, Poursoulis M, Vaissermann J. Asymmetric synthesis of pipecolic acid derivatives Tetrahedron. 48: 431-442. DOI: 10.1016/S0040-4020(01)89005-0 |
0.336 |
|
| 1991 |
Agami C, Couty F, Prince B, Puchot C. Asymmetric synthesis of N-methyl-α-amino esters from a glyoxal derived chiral heterocycle Tetrahedron. 47: 4343-4354. DOI: 10.1016/S0040-4020(01)87103-9 |
0.375 |
|
| 1990 |
Agami C, Couty F. Enantioselective Synthesis of Pipecolic Acid Derivativesviaan Ene-Iminium Cyclization Synlett. 1990: 731-732. DOI: 10.1055/S-1990-21228 |
0.368 |
|
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