Literature DB >> 30730598

Acetaldehyde Silyl Enol Ethers in Enantioselective Mukaiyama Aldol Reactions: Enzyme-Like Organocatalysis in Action.

Luca Dell'Amico1, Franca Zanardi2.   

Abstract

Touched for the very first time! It is herein highlighted how acetaldehyde silyl enol ethers undergo enantioselective Mukaiyama aldol reaction with aliphatic and aromatic aldehydes. The chemistry relies on the use of the highly efficient and substrate-selective imidodiphosphorimidate catalyst, which displays some of the features of enzymatic catalysis.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Mukaiyama aldol reaction; acetaldehyde; asymmetric synthesis; enzyme-like catalysis; organocatalysis

Year:  2019        PMID: 30730598     DOI: 10.1002/anie.201812964

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Confinement-Controlled, Either syn- or anti-Selective Catalytic Asymmetric Mukaiyama Aldolizations of Propionaldehyde Enolsilanes.

Authors:  Tynchtyk Amatov; Nobuya Tsuji; Rajat Maji; Lucas Schreyer; Hui Zhou; Markus Leutzsch; Benjamin List
Journal:  J Am Chem Soc       Date:  2021-08-26       Impact factor: 15.419

  1 in total

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