Iridium-catalyzed asymmetric hydrogenation of racemic α-substituted lactones to chiral diols-Reference-Cited by-同舟云学术

Iridium-catalyzed asymmetric hydrogenation of racemic α-substituted lactones to chiral diols

Published:2017 Issue:3 Volume:8 Page:1811-1814
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Yang Xiao-Hui¹²³⁴,Yue Hai-Tao¹²³⁴,Yu Na¹²³⁴,Li Yi-Pan¹²³⁴,Xie Jian-Hua¹²³⁴,Zhou Qi-Lin¹²³⁴⁵

Affiliation:

1. State Key Laboratory and Institute of Elemento-Organic Chemistry

2. Nankai University

3. Tianjin 300071

4. China

5. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)

Abstract

A protocol for the highly efficient iridium-catalyzed asymmetric hydrogenation of racemic α-substituted lactones via dynamic kinetic resolution is described.

Funder

National Natural Science Foundation of China

Ministry of Education of the People's Republic of China

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/SC/C6SC04609F

Reference39 articles.

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4. Ru-Catalyzed Asymmetric Hydrogenation of Racemic Aldehydes via Dynamic Kinetic Resolution: Efficient Synthesis of Optically Active Primary Alcohols

5. T. Ohkuma and R.Noyori, in The Handbook of Homogeneous Hydrogenation, ed. J. G. de Vries and C. J. Elsevier, Wiley-VCH, Weinheim, 2007, p. 1105

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