Chiral Catalysts Dually Functionalized with Amino Acid and Zn2+Complex Components for Enantioselective Direct Aldol Reactions Inspired by Natural Aldolases: Design, Synthesis, Complexation Properties, Catalytic Activities, and Mechanistic Study-Reference-Cited by-同舟云学术

Chiral Catalysts Dually Functionalized with Amino Acid and Zn2+Complex Components for Enantioselective Direct Aldol Reactions Inspired by Natural Aldolases: Design, Synthesis, Complexation Properties, Catalytic Activities, and Mechanistic Study

Published:2009-10-12 Issue:40 Volume:15 Page:10570-10584
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Itoh Susumu,Kitamura Masanori,Yamada Yasuyuki,Aoki Shin

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference177 articles.

1. Modern Aldol Reactions (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004;

2. Catalytic asymmetric aldol reactions. Use of a chiral (acyloxy)borane complex as a versatile Lewis-acid catalyst

3. New catalysts for the asymmetric aldol reaction: chiral boranes prepared from .alpha.,.alpha.-disubstituted glycine arenesulfonamides

4. Enantioselective Mukaiyama-aldol and aldol-dihydropyrone annulation reactions catalyzed by a tryptophan-derived oxazaborolidine

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