Literature DB >> 29741785

Stereoconvergent 1,4-Addition Reaction of 5H-Oxazol-4-ones with E,Z Isomeric Mixture of Alkylidene β-Ketoesters Catalyzed by Chiral Guanidines.

Tomonori Misaki1, Toshifumi Tatsumi1, Tatsumasa Okamoto1, Yusuke Hayashi1, Nari Jin1, Takashi Sugimura1.   

Abstract

A 1,4-addition reaction of 5H-oxazol-4-ones to alkylidene β-ketoesters, which was catalyzed by using chiral guanidines via a dynamic kinetic resolution process that involved geometric isomerization of the alkylidene β-ketoesters, was developed. This method allowed using E,Z isomeric mixture of various acyclic alkylidene β-ketoesters to obtain the products stereoselectively. The relation between the geometry and the stereoselectivity of products was investigated, and the derivatization of the products to the corresponding α-acyl-γ-lactone was performed.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  5H-oxazol-4-ones; alkylidene β-ketoesters; asymmetric catalysis; organocatalysis; stereoconvergent reactions

Year:  2018        PMID: 29741785     DOI: 10.1002/chem.201802271

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Stereoconvergent Conjugate Addition of Arylboronic Acids to α-Angelica Lactone Derivatives: Synthesis of Stereochemically Complex γ-Butyrolactones.

Authors:  Jessica A Griswold; Jeffrey S Johnson
Journal:  ACS Catal       Date:  2019-11-19       Impact factor: 13.084

  1 in total

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