Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Jean-Cédric Frison"'
Autor:
J.Y. Douillard, Christine Saluzzo, Stéphane Guillarme, Gilles Dujardin, Séverine Marionneau-Lambot, Jézabel Rocher, Jacques Le Pendu, Jean-Yves Le Questel, Michel Evain, Jacques Lebreton, Jean-Cédric Frison, Didier Dubreuil, Mette Diswall, Muriel Pipelier, Thibauld Oullier, Denis Jacquemin, Jérôme Graton, Julie Hunault, Virginie Blot
Publikováno v:
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2012, 55 (3), pp.1227-1241. ⟨10.1021/jm201368m⟩
Journal of Medicinal Chemistry, American Chemical Society, 2012, 55 (3), pp.1227-1241. ⟨10.1021/jm201368m⟩
We propose here the synthesis and biological evaluation of 3,4-dideoxy-GalCer derivatives. The absence of the 3- and 4-hydroxyls on the sphingoid base is combined with the introduction of mono or difluoro substituent at C3 (analogues 8 and 9, respect
Publikováno v:
Organometallics. 27:281-288
A new class of chiral N-heterocyclic carbene (NHC) precursors has been prepared incorporating a phenoxyimine moiety. Reaction between 3-((1R,2R)-2-{[1-(3,5-di-tert-butyl-2-hydroxyphenyl)meth-(E)-ylidene]amino}cyclohexyl)-1-isopropyl-4-phenyl-3H-imida
Publikováno v:
Tetrahedron. 62:6700-6706
Asymmetric Baeyer–Villiger oxidations of racemic and prochiral cyclobutanones can be performed with chiral aluminium-based Lewis acids resulting in products with good enantioselectivities in high yields. By employing substituted BINOL derivatives a
Autor:
Hasan Koyuncu, Jean-Cédric Frison, Adrian C. Whitwood, Richard E. Douthwaite, Stevan Simonovic
Publikováno v:
Organic Letters. 11:245-247
Reactions between imidazolium-imine salts and base result in C-C bond formation via intermediate N-heterocyclic carbenes. In the presence of a proximal OH moiety, carbene formation occurs via intramolecular deprotonation by phenoxide. For simple imin
Publikováno v:
Tetrahedron Letters. 45:5019-5021
Chiral dipyridylamines have been synthesized by N-arylation reactions, and the applicability of those compounds to the copper-catalyzed asymmetric allylic oxidation of cyclohexene was demonstrated.
Autor:
Jean Cédric Frison, Takehiko Yoshimitsu, Bengü Sezen, Gan B. Bajracharya, Yoshitaka Hamashima, Seijiro Matsubara, Ombretta Porta, Mikiko Sodeoka, Armin Börner, Yoshinori Yamamoto, Claudio Palomo Nicolau, Barry B. Snider, Jesffls A. Varela, Stefan Kaskel, Gerald Dyker, Aiwen Lei, Dalibor Sames, David C. Ebner, Carsten Bolm, Shun Ichi Murahashi, Brian M. Stoltz, Mikel Oiarbide, Armando Córdova, Xumu Zhang, Minsheng He, Francesco Minisci, Julien Legros, A. Ganesan, Andrea Christiansen
Publikováno v:
Handbook of C-H Transformations: Applications in Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53a374cdd9b289521d8322a676aa0928
https://doi.org/10.1002/9783527619450.ch8
https://doi.org/10.1002/9783527619450.ch8
Publikováno v:
Modern Oxidation Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3be7c51e05d722f2c762e5871f5e75a0
https://doi.org/10.1002/3527603689.ch9
https://doi.org/10.1002/3527603689.ch9
Publikováno v:
ChemInform. 36
C2-symmetric and unsymmetrically substituted 2,2′-dipyridylamines have been synthesized by sequential Buchwald–Hartwig aminations of halo-pyridines. The X-ray crystal structure of a copper dichloride complex bearing a C2-symmetric 2,2′-dipyridy
Publikováno v:
ChemInform. 35
Vaulted biaryls (VANOL and VAPOL) have been ap- plied in the aluminum-catalyzed asymmetric Baeyer-Villiger reaction of prochiral 3-substituted cyclobutanones. Optically active g-butyrolactones are obtained in high yields with enantioselectivi- ties o
Publikováno v:
Dalton Transactions. :7141
Rhodium and iridium complexes of chiral NHC-phenolimine and NHC-amine ligands have been prepared and studied for asymmetric transfer hydrogenation. X-ray and NMR spectroscopy show that for NHC-phenolimine complexes abstraction of chloride results in