Highly enantioselective Michael reaction employing cycloheptanone and cyclooctanone as nucleophiles-Reference-Cited by-同舟云学术

Highly enantioselective Michael reaction employing cycloheptanone and cyclooctanone as nucleophiles

Published:2015 Issue:1 Volume:39 Page:355-360
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Xia Ai-Bao¹²³⁴⁵,Zhao Long¹²³⁴⁵,Wang Tao¹²³⁴⁵,Zhang Yan-Peng¹²³⁴⁵,Zhong Ai-Guo⁶⁷⁸⁵,Xu Dan-Qian¹²³⁴⁵,Xu Zhen-Yuan¹²³⁴⁵

Affiliation:

1. Catalytic Hydrogenation Research Centre

2. State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology

3. Zhejiang University of Technology

4. Hangzhou

5. China

6. Department of Pharmaceutical and Chemical Engineering

7. Taizhou College

8. Linhai Zhejiang

Abstract

An organocatalytic Michael reaction of cycloheptanone and cyclooctanone with nitrodienes and nitroolefins catalyzed by primary amine catalysts has been accomplished.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/NJ/C4NJ01206B

Reference74 articles.

1. Asymmetric Organocatalysis: From Biomimetic Concepts to Applications in Asymmetric Synthesis, ed. A. Berkessel and H. Gröger, Wiley-VCH, Weinheim, 2004

2. Enantioselective Organocatalysis, ed. P. I. Dalko, Wiley-VCH, Weinheim, 2007

3. The Organic Approach to Asymmetric Catalysis

4. Enantioselective organocatalysis

5. The advent and development of organocatalysis

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