Construction of an All-Carbon Quaternary Stereocenter by the Peptide-Catalyzed Asymmetric Michael Addition of Nitromethane to β-Disubstituted α,β-Unsaturated Aldehydes-Reference-Cited by-同舟云学术

Construction of an All-Carbon Quaternary Stereocenter by the Peptide-Catalyzed Asymmetric Michael Addition of Nitromethane to β-Disubstituted α,β-Unsaturated Aldehydes

Published:2012-11-09 Issue:51 Volume:51 Page:12786-12789
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Akagawa Kengo,Kudo Kazuaki

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201206916/fullpdf

Reference99 articles.

1. Stereoselective synthesis of γ-amino acids

2. Organokatalytische asymmetrische Dominoreaktionen: eine Kaskade aus Michael-Addition und Aldehyd-α-Alkylierung

3. Organocatalytic Asymmetric Domino Reactions: A Cascade Consisting of a Michael Addition and an Aldehyde α‐Alkylation

4. Enantioselective Organocatalytic Michael Addition of Aldehydes to Nitroethylene: Efficient Access to γ2-Amino Acids

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