Ni-Catalyzed Defluorination for the Synthesis of gem-Difluoro-1,3-dienes and Their [4 + 2] Cycloaddition Reaction-Reference-Cited by-同舟云学术

Ni-Catalyzed Defluorination for the Synthesis of gem-Difluoro-1,3-dienes and Their [4 + 2] Cycloaddition Reaction

Published:2019-01-11 Issue:3 Volume:21 Page:671-674
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhou Minqi¹,Zhang Jian²,Zhang Xing-Guo¹^ORCID,Zhang Xingang²^ORCID

Affiliation:

1. College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China

2. Key Laboratory of Organofluorine Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

Funder

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

National Natural Science Foundation of China

Chinese Academy of Sciences

Natural Science Foundation of Zhejiang Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b03841

Reference37 articles.

1. Fluorine in Pharmaceuticals: Looking Beyond Intuition

2. Understanding organofluorine chemistry. An introduction to the C–F bond

3. Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design

4. Fluorine in Pharmaceutical Industry: Fluorine-Containing Drugs Introduced to the Market in the Last Decade (2001–2011)

5. Catalysis for fluorination and trifluoromethylation

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