| Year |
Citation |
Score |
| 2020 |
Badarau E, Reddy HV, Loudet A, Simon C, Trembleau L, Claerhout S, Pair E, Massip S, Breton P, Lesur B, Goldstein S, Fourquez JM, Henlin JM, Ghosez L. Productive Syntheses of Privileged Scaffolds Inspired by the Recognition of a Diels-Alder Pattern Common to three Classes of Natural Products. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32428343 DOI: 10.1002/Chem.202002372 |
0.335 |
|
| 2018 |
Péron F, Riché S, Lesur B, Hibert M, Breton P, Fourquez JM, Girard N, Bonnet D. Versatile Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines. Acs Omega. 3: 15182-15192. PMID 31458181 DOI: 10.1021/acsomega.8b01752 |
0.395 |
|
| 2010 |
Farard J, Loge C, Pfeiffer B, Lesur B, Duflos M. ChemInform Abstract: A Convenient Synthesis of 5-Arylamino-4H-pyran-4-ones Using Palladium-Catalyzed Amination. Cheminform. 41. DOI: 10.1002/chin.201004134 |
0.429 |
|
| 2009 |
Farard J, Logé C, Pfeiffer B, Lesur B, Duflos M. A convenient synthesis of 5-arylamino-4H-pyran-4-ones using palladium-catalyzed amination Tetrahedron Letters. 50: 5729-5732. DOI: 10.1016/j.tetlet.2009.07.139 |
0.393 |
|
| 2006 |
Legentil L, Lesur B, Delfourne E. Aza-analogues of the marine pyrroloquinoline alkaloids wakayin and tsitsikammamines: synthesis and topoisomerase inhibition. Bioorganic & Medicinal Chemistry Letters. 16: 427-9. PMID 16242321 DOI: 10.1016/j.bmcl.2005.09.063 |
0.323 |
|
| 2005 |
Célanire S, Descamps-François C, Lesur B, Guillaumet G, Joseph B. Synthesis of 14-membered ring jaspamide derivatives Letters in Organic Chemistry. 2: 528-531. DOI: 10.2174/1570178054640697 |
0.417 |
|
| 2004 |
Davion Y, Guillaumet G, Léger JM, Jarry C, Lesur B, Mérour JY. Synthesis of substituted 1,4-benzoxazepin-3-one derivatives Heterocycles. 63: 1093-1112. DOI: 10.1002/chin.200436163 |
0.563 |
|
| 2003 |
Davion Y, Guillaumet G, Léger JM, Jarry C, Lesur B, Mérour JY. Synthesis of 5-(4-aryl)-2-phenyl-5,6-dihydrobenzo[bl[1,5]oxazocin-4-ones Heterocycles. 60: 1793-1804. |
0.58 |
|
| 1989 |
Roush WR, Michaelides MR, Tai DF, Lesur BM, Chong WKM, Harris DJ. A highly stereoselective synthesis of (+)-olivin, the aglycon of olivomycin A Journal of the American Chemical Society. 111: 2984-2995. DOI: 10.1021/Ja00190A036 |
0.571 |
|
| 1989 |
ROUSH WR, MICHAELIDES MR, TAI DF, LESUR BM, CHONG WKM, HARRIS DJ. ChemInform Abstract: A Highly Stereoselective Synthesis of (+)-Olivin, the Aglycon of Olivomycin A. Cheminform. 20. DOI: 10.1002/chin.198932317 |
0.581 |
|
| 1989 |
Roush WR, Michaelides MR, Tai DF, Lesur BM, Chong WKM, Harris DJ. A highly stereoselective synthesis of (+)-olivin, the aglycon of olivomycin A Journal of the American Chemical Society. 111: 2984-2995. |
0.601 |
|
| 1983 |
Roush WR, Lesur BM. Stereochemistry of Vinyl Cuprate Additions to Carbohydrate-Derived Enones and α,β-Unsaturated Esters Tetrahedron Letters. 24: 2231-2234. DOI: 10.1016/S0040-4039(00)81891-2 |
0.468 |
|
| 1983 |
Roush WR, Harris DJ, Lesur BM. Studies on the Synthesis of Olivin: Diastereoselective Synthesis of a Functionalized D-Fucose Derivative Tetrahedron Letters. 24: 2227-2230. DOI: 10.1016/S0040-4039(00)81890-0 |
0.569 |
|
| 1983 |
ROUSH WR, HARRIS DJ, LESUR BM. ChemInform Abstract: STUDIES ON THE SYNTHESIS OF OLIVIN: DIASTEREOSELECTIVE SYNTHESIS OF A FUNCTIONALIZED D-FUCOSE DERIVATIVE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198339356 |
0.567 |
|
| 1983 |
ROUSH WR, LESUR BM. ChemInform Abstract: STEREOCHEMISTRY OF VINYL CUPRATE ADDITIONS TO CARBOHYDRATE-DERIVED ENONES AND α,β-UNSATURATED ESTERS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198339111 |
0.459 |
|
| 1982 |
De Lombaert S, Lesur B, Ghosez L. Synthesis with a-Cyanoenamines. 2-Diethylamino 4-Lithio-4-phenylthio-2-butenonitrile as a B-Carboxyl vinyl anion equivalent. Tetrahedron Letters. 23: 4251-4254. DOI: 10.1016/S0040-4039(00)88717-1 |
0.351 |
|
| 1979 |
Lesur B, Toye J, Chantrenne M, Ghosez L. Base-catalysed alkylations and conjugated additions of α-cyanoenamines : A method for chain extension at the β-carbon of tertiary amides Tetrahedron Letters. 20: 2835-2838. DOI: 10.1016/S0040-4039(01)86429-7 |
0.341 |
|
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