Catalytic Asymmetric Mannich Reaction of Glycine Derivatives with
<i>N</i>
‐Tosylimines using Copper(I)/TF‐BiphamPhos Complex
作者:Gang Liang、Min‐Chao Tong、Haiyan Tao、Chun‐Jiang Wang
DOI:10.1002/adsc.201000252
日期:2010.10.9
The direct asymmetric Mannichreaction of glycine Schiff bases with N-tosylimines has been developed with the tetrakis(acetonitrile)copper(I) tetrafluoroborate [Cu(CH3CN)4BF4]/TF-BiphamPhos complex. This catalytic system performs well over a broad range of substrates, furnishing anti-adducts of various α,β-diamino acid esters in good yields with up to 94:6 diastereoselectivity and 97% 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.