| Year |
Citation |
Score |
| 2017 |
Choudhury SK, Rout P, Parida BB, Florent J, Johannes L, Phaomei G, Bertounesque E, Rout L. Metal-Free Activation of C(sp3
)-H Bond, and a Practical and Rapid Synthesis of Privileged 1-Substituted 1,2,3,4-Tetrahydroisoquinolines European Journal of Organic Chemistry. 2017: 5275-5292. DOI: 10.1002/Ejoc.201700471 |
0.585 |
|
| 2016 |
Rout L, Parida BB, Florent JC, Johhanne L, Choudhury SK, Phaomei G, Joe S, Bertounesque E. Metal-Free Activation of C(sp)-H Bond of Aromatic Acetylene. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27504988 DOI: 10.1002/Chem.201603003 |
0.536 |
|
| 2012 |
Carrër A, Brinet D, Florent JC, Rousselle P, Bertounesque E. Palladium-catalyzed direct arylation of polysubstituted benzofurans. The Journal of Organic Chemistry. 77: 1316-27. PMID 22141919 DOI: 10.1021/Jo202060K |
0.457 |
|
| 2011 |
Carrër A, Florent JC, Auvrouin E, Rousselle P, Bertounesque E. Synthesis of 3-aryl-2-arylamidobenzofurans based on the Curtius rearrangement. The Journal of Organic Chemistry. 76: 2502-20. PMID 21391629 DOI: 10.1021/jo102265b |
0.342 |
|
| 2011 |
Commandeur C, Florent J, Rousselle P, Bertounesque E. Easy Access to Pyranoacridines, Pyranoxanthenes, and Arylchromenes Through a Domino Reaction European Journal of Organic Chemistry. 2011: 1447-1451. DOI: 10.1002/EJOC.201001598 |
0.356 |
|
| 2011 |
Commandeur C, Florent J, Rousselle P, Bertounesque E. ChemInform Abstract: Easy Access to Pyranoacridines, Pyranoxanthenes, and Arylchromenes Through a Domino Reaction. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201128027 |
0.367 |
|
| 2010 |
Courme C, Gresh N, Vidal M, Lenoir C, Garbay C, Florent JC, Bertounesque E. Synthesis of aryl phosphates based on pyrimidine and triazine scaffolds. European Journal of Medicinal Chemistry. 45: 244-55. PMID 19906464 DOI: 10.1016/J.Ejmech.2009.10.003 |
0.38 |
|
| 2010 |
Courme C, Gresh N, Lenoir C, Vidal M, Garbay C, Florent J, Bertounesque E. ChemInform Abstract: Synthesis of Bis-Aryl Phosphates Based on Triazine Scaffold. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201035223 |
0.313 |
|
| 2008 |
Courme C, Gillon S, Gresh N, Vidal M, Garbay C, Florent JC, Bertounesque E. Terminal alkyne-functionalized triazine by Sonogashira coupling: synthesis of a potential cell signalling inhibitor via click chemistry Tetrahedron Letters. 49: 4542-4545. DOI: 10.1016/J.Tetlet.2008.05.050 |
0.335 |
|
| 2008 |
Dorbec M, Florent J, Monneret C, Rager M, Fosse C, Bertounesque E. Synthesis of Novel Angular Heterocyclic Lignans by an InCl3-Catalyzed Friedel–Crafts-Type Cyclization European Journal of Organic Chemistry. 2008: 1723-1731. DOI: 10.1002/Ejoc.200701027 |
0.308 |
|
| 2008 |
Dorbec M, Florent J, Monneret C, Rager M, Fosse C, Bertounesque E. ChemInform Abstract: Synthesis of Novel Angular Heterocyclic Lignans by an InCl3-Catalyzed Friedel-Crafts-Type Cyclization. Cheminform. 39. DOI: 10.1002/CHIN.200830116 |
0.317 |
|
| 2007 |
Bertounesque E, Meresse P, Monneret C, Florent J. Synthetic approach to condensed heterocyclic analogues from etoposide revisited. Synthesis of A-ring pyridazine etoposide Tetrahedron Letters. 48: 5781-5784. DOI: 10.1016/J.Tetlet.2007.06.105 |
0.313 |
|
| 2006 |
Dorbec M, Florent J, Monneret C, Rager M, Bertounesque E. Synthesis of γ-Lactam Lignans via Aza-Michael Addition. Cheminform. 37. DOI: 10.1055/S-2006-932485 |
0.3 |
|
| 2006 |
Dorbec M, Florent J, Monneret C, Rager M, Bertounesque E. 1-Aryltetralin privileged structure-based libraries: parallel synthesis of N-aryl and N-biaryl γ-lactam lignans Tetrahedron. 62: 11766-11781. DOI: 10.1016/J.Tet.2006.09.026 |
0.306 |
|
| 2004 |
Meresse P, Monneret C, Bertounesque E. Synthesis of podophyllotoxin analogues: δ-lactone-containing picropodophyllin, podophyllotoxin and 4′-demethyl-epipodophyllotoxin derivatives Tetrahedron. 60: 2657-2671. DOI: 10.1016/J.Tet.2004.01.017 |
0.332 |
|
| 1999 |
Smith AB, Friestad GK, Barbosa J, Bertounesque E, Hull KG, Iwashima M, Qiu Y, Salvatore BA, Spoors PG, Duan JJW. Total synthesis of (+)-calyculin A and (-)-calyculin B: Asymmetric synthesis of the C(9-25) spiroketal dipropionate subunit Journal of the American Chemical Society. 121: 10468-10477. DOI: 10.1021/Ja992134M |
0.353 |
|
| 1996 |
Bertounesque E, Imbert T, Monneret C. Synthesis of podophyllotoxin A-ring pyridazine analogue Tetrahedron. 52: 14235-14246. DOI: 10.1016/0040-4020(96)00862-9 |
0.306 |
|
| 1988 |
Bellassoued M, Dubois J, Bertounesque E. New development of the Mukaiyama reaction: One pot synthesis of β-chloro acids and esters Tetrahedron Letters. 29: 1275-1278. DOI: 10.1016/S0040-4039(00)80275-0 |
0.365 |
|
| 1988 |
BELLASSOUED M, DUBOIS JE, BERTOUNESQUE E. ChemInform Abstract: New Development of the Mukaiyama Reaction: One-Pot Synthesis of β-Chloro Acids and Esters. Cheminform. 19. DOI: 10.1002/chin.198831127 |
0.358 |
|
| 1986 |
Bellassoued M, Dubois J, Bertounesque E. Erythro selective cross aldol reaction via α-silyl trimethylsilyl esters. Tetrahedron Letters. 27: 2623-2626. DOI: 10.1016/S0040-4039(00)84601-8 |
0.524 |
|
| 1986 |
BELLASSOUED M, DUBOIS J, BERTOUNESQUE E. ChemInform Abstract: Erythro Selective Cross Aldol Reaction via α-Silyl Trimethylsilyl Esters. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198647139 |
0.39 |
|
| 1986 |
DUBOIS J, AXIOTIS G, BERTOUNESQUE E. ChemInform Abstract: Chromium(II) Chloride: A New Reagent for Cross-Aldol Reactions. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198607156 |
0.357 |
|
| 1985 |
Dubois J, Axiotis G, Bertounesque E. Chromium (II) chloride : a new reagent for cross-aldol reactions Tetrahedron Letters. 26: 4371-4372. DOI: 10.1016/S0040-4039(00)98737-9 |
0.521 |
|
| 1985 |
DUBOIS J, AXIOTIS G, BERTOUNESQUE E. ChemInform Abstract: KETENE BIS(TRIMETHYLSILYL) ACETALS. CROSS-ALDOL CONDENSATION WITH ALDEHYDES. STEREOCHEMISTRY OF THE REACTION Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198506159 |
0.408 |
|
| 1984 |
Dubois J, Axiotis G, Bertounesque E. Ketene bis(trimethylsilyl) acetals. Cross-Aldol condensation with aldehydes. Stereochemistry of the reaction Tetrahedron Letters. 25: 4655-4658. DOI: 10.1016/S0040-4039(01)91225-0 |
0.55 |
|
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