Photoredox-Catalyzed Decarboxylative C-H Acylation of Heteroarenes

Wei Jia; Yong Jian; Binbin Huang; Chao Yang; Wujiong Xia

doi:10.1055/s-0037-1609911

Photoredox-Catalyzed Decarboxylative C-H Acylation of Heteroarenes

Wei Jia
, Yong Jian
, Binbin Huang
, Chao Yang^*
, Wujiong Xia

^*Corresponding author for this work

Harbin Institute of Technology Shenzhen

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

36 Scopus citations

Abstract

A mild, environmentally friendly, and regioselective acylation of heterocycles with inexpensive carboxylic acids is reported via photoredox catalysis. The strategy is highlighted with good functional group tolerance and substrate scope which could rapidly realize the acylation of various heterocyclic compounds.

Original language	English
Pages (from-to)	1881-1886
Number of pages	6
Journal	Synlett
Volume	29
Issue number	14
DOIs	https://doi.org/10.1055/s-0037-1609911
State	Published - 2018
Externally published	Yes

Keywords

2,2-diethoxyacetic acid
C-H functionalization
acylation
heterocycles
α-keto acids

Access to Document

10.1055/s-0037-1609911

Cite this

@article{9cc73c6d572047ef84993ed3ef1d8ca9,

title = "Photoredox-Catalyzed Decarboxylative C-H Acylation of Heteroarenes",

abstract = "A mild, environmentally friendly, and regioselective acylation of heterocycles with inexpensive carboxylic acids is reported via photoredox catalysis. The strategy is highlighted with good functional group tolerance and substrate scope which could rapidly realize the acylation of various heterocyclic compounds.",

keywords = "2,2-diethoxyacetic acid, C-H functionalization, acylation, heterocycles, α-keto acids",

author = "Wei Jia and Yong Jian and Binbin Huang and Chao Yang and Wujiong Xia",

note = "Publisher Copyright: {\textcopyright} Georg Thieme Verlag Stuttgart New York.",

year = "2018",

doi = "10.1055/s-0037-1609911",

language = "英语",

volume = "29",

pages = "1881--1886",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "14",

}

TY - JOUR

T1 - Photoredox-Catalyzed Decarboxylative C-H Acylation of Heteroarenes

AU - Jia, Wei

AU - Jian, Yong

AU - Huang, Binbin

AU - Yang, Chao

AU - Xia, Wujiong

N1 - Publisher Copyright: © Georg Thieme Verlag Stuttgart New York.

PY - 2018

Y1 - 2018

N2 - A mild, environmentally friendly, and regioselective acylation of heterocycles with inexpensive carboxylic acids is reported via photoredox catalysis. The strategy is highlighted with good functional group tolerance and substrate scope which could rapidly realize the acylation of various heterocyclic compounds.

AB - A mild, environmentally friendly, and regioselective acylation of heterocycles with inexpensive carboxylic acids is reported via photoredox catalysis. The strategy is highlighted with good functional group tolerance and substrate scope which could rapidly realize the acylation of various heterocyclic compounds.

KW - 2,2-diethoxyacetic acid

KW - C-H functionalization

KW - acylation

KW - heterocycles

KW - α-keto acids

UR - https://www.scopus.com/pages/publications/85051935658

U2 - 10.1055/s-0037-1609911

DO - 10.1055/s-0037-1609911

M3 - 文章

AN - SCOPUS:85051935658

SN - 0936-5214

VL - 29

SP - 1881

EP - 1886

JO - Synlett

JF - Synlett

IS - 14

ER -

Photoredox-Catalyzed Decarboxylative C-H Acylation of Heteroarenes

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this