Visible-Light-Induced Radical <i>gem</i>-Iodoallylation of 2,2,2-Trifluorodiazoethane-Reference-Cited by-同舟云学术

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Visible-Light-Induced Radical gem-Iodoallylation of 2,2,2-Trifluorodiazoethane

Published:2023-03-13 Issue:11 Volume:25 Page:1958-1962
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Yu¹,Pang Tengfei¹,Yao Weijun²^ORCID,Zhong Fangrui¹^ORCID,Wu Guojiao¹^ORCID

Affiliation:

1. Hubei Key Laboratory of Bioinorganic Chemistry & Materia Medica, Hubei Engineering Research Center for Biomaterials and Medical Protective Materials, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology (HUST), 1037 Luoyu Road, Wuhan 430074, China

2. Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018, P.R. China

Funder

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

Central University Basic Research Fund 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.3c00464

Reference52 articles.

1. Organic fluorine compounds: a great opportunity for enhanced materials properties

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

3. Current Contributions of Organofluorine Compounds to the Agrochemical Industry

4. Electrophilic Trifluoromethylation by Use of Hypervalent Iodine Reagents

5. Advances in Catalytic Enantioselective Fluorination, Mono-, Di-, and Trifluoromethylation, and Trifluoromethylthiolation Reactions

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2. Visible-Light-Promoted Radical gem-Selenosulfonylation or -Iodosulfonylation of 2,2,2-Trifluorodiazoethane under Photosensitizer-Free Conditions;Organic Letters;2024-06-10

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