The AgOAc/ThioClickFerrophos complex catalyzed the asymmetric Mannichreaction of glycine Schiff base with N-tosylimines effectively to give a mixture of syn and anti adducts (syn/anti = 60/40−70/30) at high yields with high enantioselectivities (up to 98% ee). The complex also catalyzed the asymmetric amination of glycine Schiff base with di-tert-butyl azodicarboxylate with high enantioselectivity
Synthesis of α,β-diamino acid derivatives via asymmetric Mannich reactions of glycine imino esters catalyzed by a chiral phosphoramidite·silver complex
作者:Alberto Cayuelas、Loane Serrano、Carmen Nájera、José M. Sansano
DOI:10.1016/j.tetasy.2014.11.009
日期:2014.12
AgOTf phosphoramidite complexes efficiently catalyze the enantioselective Mannich-type reaction between benzophenone-imine glycine methyl ester and N-tosyl aldimines in the absence of a base. The corresponding syn-adducts, which are the direct precursors of alpha,beta-diamino acids, are obtained with moderate to good syn-diastereoselectivities (up to 9:1) and high enantioselectivities (up to 99% ee). (C) 2014 Elsevier Ltd. All rights reserved.