Photoredox-Catalyzed C–H Arylation of Internal Alkenes to Tetrasubstituted Alkenes: Synthesis of Tamoxifen-Reference-Cited by-同舟云学术

Photoredox-Catalyzed C–H Arylation of Internal Alkenes to Tetrasubstituted Alkenes: Synthesis of Tamoxifen

Published:2017-11-02 Issue:22 Volume:19 Page:6248-6251
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Quannan¹²^ORCID,Yang Xiaoge¹^ORCID,Wu Ping¹²^ORCID,Yu Zhengkun¹³^ORCID

Affiliation:

1. Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, P. R. China

2. University of Chinese Academy of Sciences, Beijing 100049, P. R. China

3. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, P. R. China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b03223

Reference55 articles.

1. Recent Advances in Efficient and Selective Synthesis of Di-, Tri-, and Tetrasubstituted Alkenes via Pd-Catalyzed Alkenylation−Carbonyl Olefination Synergy

2. Stereocontrolled Synthesis of Tetrasubstituted Olefins

3. Mizoroki–Heck Cyclizations of Amide Derivatives for the Introduction of Quaternary Centers

4. Recent Advances in Asymmetric Hydrogenation of Tetrasubstituted Olefins

5. Decarboxylative alkenylation

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