Enantioselective Michael addition of malonates to α,β-unsaturated ketones catalyzed by 1,2-diphenylethanediamine-Reference-Cited by-同舟云学术

Enantioselective Michael addition of malonates to α,β-unsaturated ketones catalyzed by 1,2-diphenylethanediamine

Published:2018 Issue:73 Volume:8 Page:41699-41704
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Wang Wei¹²³⁴^ORCID,Ye Ling⁵⁶⁷⁴,Shi Zhichuan¹²³⁴,Zhao Zhigang¹²³⁴,Li Xuefeng¹²³⁴^ORCID

Affiliation:

1. College of Chemistry and Environment Protection Engineering

2. Southwest Minzu University

3. Chengdu 610041

4. China

5. Faculty of Geosciences and Environmental Engineering

6. Southwest Jiaotong University

7. Chengdu 610031

Abstract

1,2-Diphenylethanediamine could be directly utilized to promote the Michael addition of malonates and β-ketoesters to various α,β-unsaturated ketones.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA07809B

Reference67 articles.

1. Enantioselective Conjugate Additions

2. Recent Advances in Catalytic Enantioselective Michael Additions

3. Recent Advances in Metal-Catalyzed Asymmetric Conjugate Additions

4. Recent Advances in Asymmetric Organocatalytic 1,4‐Conjugate Additions

5. Organocatalytic asymmetric conjugate additions

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