Organophotoredox-Catalyzed Formation of Alkyl-Aryl and -Alkyl C-S/Se Bonds from Coupling of Redox-Active Esters with Thio/Selenosulfonates

Yue Dong; Peng Ji; Yueteng Zhang; Changqing Wang; Xiang Meng; Wei Wang

doi:10.1021/acs.orglett.0c03624

Organophotoredox-Catalyzed Formation of Alkyl-Aryl and -Alkyl C-S/Se Bonds from Coupling of Redox-Active Esters with Thio/Selenosulfonates

Yue Dong
, Peng Ji
, Yueteng Zhang
, Changqing Wang
, Xiang Meng
, Wei Wang

Pharmacology and Toxicology

Research output: Contribution to journal › Article › peer-review

55 Scopus citations

Abstract

A mild organophotoredox synthetic protocol for forming a Csp3-S/Se bond by reacting widespread redox-active esters with thio/selenosulfonates has been developed. The power of the synthetic manifold is fueled by an unprecedented broad substrate scope and wide functional group tolerance.

Original language	English (US)
Pages (from-to)	9562-9567
Number of pages	6
Journal	Organic Letters
Volume	22
Issue number	24
DOIs	https://doi.org/10.1021/acs.orglett.0c03624
State	Published - Dec 18 2020

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/acs.orglett.0c03624

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title = "Organophotoredox-Catalyzed Formation of Alkyl-Aryl and -Alkyl C-S/Se Bonds from Coupling of Redox-Active Esters with Thio/Selenosulfonates",

abstract = "A mild organophotoredox synthetic protocol for forming a Csp3-S/Se bond by reacting widespread redox-active esters with thio/selenosulfonates has been developed. The power of the synthetic manifold is fueled by an unprecedented broad substrate scope and wide functional group tolerance.",

author = "Yue Dong and Peng Ji and Yueteng Zhang and Changqing Wang and Xiang Meng and Wei Wang",

note = "Publisher Copyright: {\textcopyright} 2020 American Chemical Society.",

year = "2020",

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language = "English (US)",

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AU - Dong, Yue

AU - Ji, Peng

AU - Zhang, Yueteng

AU - Wang, Changqing

AU - Meng, Xiang

AU - Wang, Wei

PY - 2020/12/18

Y1 - 2020/12/18

N2 - A mild organophotoredox synthetic protocol for forming a Csp3-S/Se bond by reacting widespread redox-active esters with thio/selenosulfonates has been developed. The power of the synthetic manifold is fueled by an unprecedented broad substrate scope and wide functional group tolerance.

AB - A mild organophotoredox synthetic protocol for forming a Csp3-S/Se bond by reacting widespread redox-active esters with thio/selenosulfonates has been developed. The power of the synthetic manifold is fueled by an unprecedented broad substrate scope and wide functional group tolerance.

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UR - https://www.scopus.com/pages/publications/85098742041#tab=citedBy

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DO - 10.1021/acs.orglett.0c03624

M3 - Article

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AN - SCOPUS:85098742041

SN - 1523-7060

VL - 22

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JO - Organic Letters

JF - Organic Letters

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ER -

Organophotoredox-Catalyzed Formation of Alkyl-Aryl and -Alkyl C-S/Se Bonds from Coupling of Redox-Active Esters with Thio/Selenosulfonates

Abstract

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