A highly enantioselective Friedel–Crafts reaction of 3,5-dimethoxylphenol with nitroolefins mediated by a bifunctional quinine derived thiourea catalyst-Reference-Cited by-同舟云学术

A highly enantioselective Friedel–Crafts reaction of 3,5-dimethoxylphenol with nitroolefins mediated by a bifunctional quinine derived thiourea catalyst

Published:2017 Issue:16 Volume:15 Page:3401-3407
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Han Xiaoyu¹²³⁴⁵^ORCID,Ye Can¹²³⁴⁵,Chen Fenfen¹²³⁴⁵,Chen Qu¹²³⁴⁵,Wang Yongjiang¹²³⁴⁵,Zeng Xiaofei⁶⁷⁸⁹¹⁰

Affiliation:

1. Zhejiang Provincial Key Laboratory for Chemical & Biological Processing Technology of Farm Products

2. School of Biological and Chemical Engineering/School of Light Industry

3. Zhejiang University of Science and Technology

4. Hangzhou

5. China

6. College of Material

7. Chemistry and Chemical Engineering

8. Hangzhou Normal University

9. Hangzhou 310036

10. P. R. China

Abstract

A useful and highly enantioselective Friedel–Crafts reaction of 3,5-dimethoxylphenol with nitroolefins catalyzed by a bifunctional quinine derived thiourea catalyst was developed.

Funder

Natural Science Foundation of Zhejiang Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB00372B

Reference79 articles.

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