Nickel‐Catalyzed Thioesterification Enabled by a Visible‐Light Organophotoredox Catalyst under Mild Conditions-Reference-Cited by-同舟云学术

Nickel‐Catalyzed Thioesterification Enabled by a Visible‐Light Organophotoredox Catalyst under Mild Conditions

Published:2022-01-05 Issue: Volume: Page:
ISSN:2367-0932
Container-title:ChemPhotoChem
language:en
Short-container-title:ChemPhotoChem

Author:

Zheng Wanyao¹,Xu Yongjie¹,Lin Luqing¹²^ORCID

Affiliation:

1. Zhangdayu School of Chemistry Dalian University of Technology No. 2 Linggong Road, Gangjingzi District Dalian 116024 Liaoning China

2. Global Station for Biosurfaces and Drug Discovery Global Institution for Collaborative Research and Education (GI-CoRE) Hokkaido University Kita-12 Nishi-6 Sapporo Hokkaido 060-0812 Japan

Funder

Liaoning Revitalization Talents Program

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cptc.202100264

Reference65 articles.

2. A. d Meijere S. Bräse M. Oestreich Metal-Catalyzed Cross-Coupling Reactions and More Wiley New York 2014;

4. A General and Long-Lived Catalyst for the Palladium-Catalyzed Coupling of Aryl Halides with Thiols

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1. General electron–donor–acceptor complex mediated thioesterification reaction via site-selective C–H functionalization using aryl sulfonium Salts;Green Chemistry;2024

2. C−S Cross‐Coupling Reactions Catalyzed by Well‐Defined Copper and Nickel Complexes;European Journal of Organic Chemistry;2022-08-16

3. Visible-Light-Driven Thioesterification of Aryl Halides with Potassium Thiocarboxylates: Transition-Metal Catalyst-Free Incorporation of Sulfur Functionalities into an Aromatic Ring;The Journal of Organic Chemistry;2022-06-02