Catalyst- and solvent-free aminolysis of the asymmetric derivatives of Evans’ chiral <i>N</i>-acyloxazolidinones: enantioselective synthesis of chiral amides and its applications-Reference-Cited by-同舟云学术

Catalyst- and solvent-free aminolysis of the asymmetric derivatives of Evans’ chiral N-acyloxazolidinones: enantioselective synthesis of chiral amides and its applications

Published:2022 Issue:11 Volume:24 Page:4405-4413
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Lu Hui-Rong¹,Geng Hui¹,Ding Guan-Tian¹,Huang Pei-Qiang¹^ORCID

Affiliation:

1. Department of Chemistry, Fujian Provincial Key Laboratory of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian 361005, P. R. China

Abstract

We report a convenient method for the aminolysis of N-acyloxazolidinone-derived asymmetric products and the direct conversion of the resulting secondary amides into diverse classes of compounds.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/GC/D2GC00662F

Reference96 articles.

1. Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates

2. Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives