An approach to highly efficient reduction of β-enamino esters: A convenient synthesis of β-amino esters-Reference-Cited by-同舟云学术

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An approach to highly efficient reduction of β-enamino esters: A convenient synthesis of β-amino esters

Published:2019-05 Issue:5-6 Volume:43 Page:196-200
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Zhang Xingxian¹,Mi Nengju¹,Liu Hongtao¹,Liu Yingshuai¹

Affiliation:

1. College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, P.R. China

Abstract

Chemoselective reduction of β-enamino esters with NaBH(OAc)3promoted by MgI2etherate affords the corresponding β-amino esters in excellent yields in a short time under mild conditions.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.1177/1747519819858688

Reference43 articles.

1. 1,3-Amino alcohols from 4-amino-1-aza dienes. Diastereo- and enantioselective approach to the four diastereoisomers of the N-terminal amino acid component of nikkomycins B and BX

2. Model Reactions for the Stereo-Controlled Synthesis of Aminopolyols; Reduction of Isoxazolines with Free or Protected Hydroxy Groups in Position 4 or in Side Chains

3. Tremor-Producing Aminopropanols

4. Carbenes and the oxygen-hydrogen bond: 3-cyclopentenylidene. A novel approach to bis(homocyclopropenyl) cations

5. Highly enantioselective and diastereoselective synthesis of β-amino acid esters and β-lactams from achiral esters and imines

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