Synthetic and Mechanistic Implications of Chlorine Photoelimination in Nickel/Photoredox C(sp3)–H Cross-Coupling-Reference-Cited by-同舟云学术

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Synthetic and Mechanistic Implications of Chlorine Photoelimination in Nickel/Photoredox C(sp3)–H Cross-Coupling

Published:2021-01-29 Issue:4 Volume:54 Page:988-1000
ISSN:0001-4842
Container-title:Accounts of Chemical Research
language:en
Short-container-title:Acc. Chem. Res.

Author:

Kariofillis Stavros K.¹^ORCID,Doyle Abigail G.¹^ORCID

Affiliation:

1. Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States

Funder

Princeton University

Division of Graduate Education

U.S. Department of Energy

National Institute of General Medical Sciences

BioLEC

Publisher

American Chemical Society (ACS)

Subject

General Medicine,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.0c00694

Reference75 articles.

1. Direct C(sp3)–H Cross Coupling Enabled by Catalytic Generation of Chlorine Radicals

2. Nickel/Photoredox-Catalyzed Methylation of (Hetero)aryl Chlorides Using Trimethyl Orthoformate as a Methyl Radical Source

3. Direct C–C Bond Formation from Alkanes Using Ni-Photoredox Catalysis

4. 3d-d Excited States of Ni(II) Complexes Relevant to Photoredox Catalysis: Spectroscopic Identification and Mechanistic Implications

5. Photoredox Catalysis in Organic Chemistry

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