Highly Regio‐ and Enantioselective Hydrosilylation of gem ‐Difluoroalkenes by Nickel Catalysis-Reference-Cited by-同舟云学术

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Highly Regio‐ and Enantioselective Hydrosilylation of gem ‐Difluoroalkenes by Nickel Catalysis

Published:2022-01-12 Issue: Volume: Page:
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angewandte Chemie

Author:

Bai Dachang¹²^ORCID,Wu Fen¹,Chang Lingna¹,Wang Manman¹,Wu Hao¹,Chang Junbiao¹

Affiliation:

1. NMPA Key Laboratory for Research and Evaluation of Innovative Drug Key Laboratory of Green Chemical Media and Reactions Ministry of Education School of Chemistry and Chemical Engineering Henan Normal University Xinxiang 453007 China

2. State Key Laboratory of Organometallic Chemistry Shanghai Institute of Organic Chemistry Chinese Academy of Sciences Shanghai 200032 P.R. China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202114918

Reference121 articles.

2. Modern Fluoroorganic Chemistry

3. Fluorine in medicinal chemistry

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

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enantioselective Nickel‐Catalyzed Hydrosilylation of 1,1‐Disubstituted Allenes;Angewandte Chemie International Edition;2023-02-07

2. Enantioselective Nickel‐Catalyzed Hydrosilylation of 1,1‐Disubstituted Allenes;Angewandte Chemie;2023-02-07

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