Asymmetric Dearomatization of β‐Naphthols through a Bifunctional‐Thiourea‐Catalyzed Michael Reaction-Reference-Cited by-同舟云学术

Asymmetric Dearomatization of β‐Naphthols through a Bifunctional‐Thiourea‐Catalyzed Michael Reaction

Published:2015-10-14 Issue:49 Volume:54 Page:14929-14932
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Wang Shou‐Guo¹,Liu Xi‐Jia¹,Zhao Qun‐Chao¹,Zheng Chao¹,Wang Shao‐Bo¹,You Shu‐Li¹²

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032 (China) http://shuliyou.sioc.ac.cn/

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

Funder

National Basic Research Program of China

NSFC

Chinese Academy of Sciences

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201507998

Reference100 articles.

1. For selected reviews on dearomatization reactions see:

2. Transition-Metal-Mediated Dearomatization Reactions

3. Two-electron phenolic oxidations using phenyliodonium dicarboxylates

4. Dearomatization via η6-Arene Complexes

5. The Dearomatization of Arenes by Dihapto-Coordination

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