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Probing electronic and regioisomeric control in an asymmetric Henry reaction catalyzed by camphor-imidazoline ligands
Year: 2009
Type of publication: článek v odborném periodiku
Name of source: Tetrahedron Letters
Publisher name: Pergamon-Elsevier Science Ltd.
Place: Oxford
Page from-to: 3042-3045
Titles:
Language Name Abstract Keywords
cze Probing electronic and regioisomeric control in an asymmetric Henry reaction catalyzed by camphor-imidazoline ligands Z výchozího (R)-kafrdiaminu bylo připraveno 13 nových anelovaných imidazolinových ligandů, ve výtěžcích až 94%.
eng Probing electronic and regioisomeric control in an asymmetric Henry reaction catalyzed by camphor-imidazoline ligands Starting from (R)-camphordiamine, 13 new camphor-annulated imidazoline ligands are synthesized in good yields as two regioisomeric series. Yields of up to 94% and good enantioselectivities up to 67% are achieved for the copper(II)-catalyzed Henry reaction giving the product stereoselectively according to the regioisomer used. (R)-camphordiamine, camphor-annulated imidazoline ligands