Jean Jacques
Affiliations: | Collège de France, Paris, Île-de-France, France |
Area:
chemistry of estrogen, stereochemistryWebsite:
http://fr.wikipedia.org/wiki/Jean_JacquesGoogle:
"Jean Jacques"Mean distance: 10.35
Children
Sign in to add trainee| Henri B. Kagan | grad student | 1960 | College de France |
| Andre Collet | grad student | 1973 | College de France (Paris) |
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Publications
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| Schouteeten A, Christidis Y, Mattioda G, et al. (2010) Préparation de la D (‐) Phénylglycine: Mise au Point D'Un Dedoublement par Entraînement Bulletin Des SociéTéS Chimiques Belges. 88: 897-904 |
| Martin RH, Flammang‐Barbieux M, Dvolaitzky M, et al. (2010) Configuration et Réactions des Acides 2-méthyl-3-(6-Méthoxy-2-Naphtyl)-3-Penténoique et Hexénoïque Bulletin Des SociéTéS Chimiques Belges. 81: 467-477 |
| Jacques J. (1999) Grégoire Wyrouboff (1843–1913) et la chimie positive Comptes Rendus De L Academie Des Sciences Serie Ii Fascicule C-Chimie. 2: 467-470 |
| Morales-Alanis H, Brienne M-, Jacques J, et al. (1986) Antiandrogenic Activity of a Series of Des-A-Steroid Derivatives. Cheminform. 17 |
| Morales-Alanis H, Brienne MJ, Jacques J, et al. (1985) Antiandrogenic activity of a series of des-A-steroid derivatives. Journal of Medicinal Chemistry. 28: 1796-1803 |
| Brienne M, Collet A, Jacques J. (1983) A Convenient Optical Resolution ofsec-Phenethyl Alcohol by Preferential Crystallization of Its 3,5-Dinitrobenzoate Synthesis. 1983: 704-705 |
| Destrade C, Gasparoux H, Foucher P, et al. (1983) Molécules discoïdes et polymorphisme mésomorphe Journal of Computers. 80: 137-148 |
| Canceill J, Collet A, Jacques J. (1982) Application of the exciton chirality method for the stereochemical assignment of remote groups. Determination of the α- or β-configuration of a 2-hydroxy-substituent in 2,17- and 2,16-dihydroxy-A-nor-5α-androstane and -estrane derivatives Journal of the Chemical Society-Perkin Transactions 1. 13: 83-89 |
| Collet A, Gabard J, Jacques J, et al. (1981) Synthesis and absolute configuration of chiral (C3) cyclotriveratrylene derivatives. Crystal structure of (M)-(–)-2,7,12-triethoxy-3,8,13-tris-[(R)-1-methoxycarbonylethoxy]-10,15-dihydro-5H-tribenzo[a,d,g]-cyclononene Journal of the Chemical Society-Perkin Transactions 1. 12: 1630-1638 |
| Jacques J, Leclercq M, Brienne M. (1981) La formation de sels augmente-t-elle la fréquence des dédoublements spontanés? Tetrahedron. 37: 1727-1733 |