Chloride-mediated electrochemical synthesis of oxazolines

Wenda Wu; Gang Li; T. Leo Liu

doi:10.1016/j.checat.2021.10.003

Chloride-mediated electrochemical synthesis of oxazolines

Wenda Wu
, Gang Li
, T. Leo Liu

Research output: Contribution to journal › Comment/debate

2 Scopus citations

Abstract

In this issue of Chem Catalysis, Liang et al. report an efficient electrochemical cyclization reaction of alkenes and amides to produce oxazolines with broad substrate scopes and good selectivities. A chloronium species generated by the chloride-mediated redox catalysis is proposed as a key intermediate.

Original language	English
Pages (from-to)	966-967
Number of pages	2
Journal	Chem Catalysis
Volume	1
Issue number	5
DOIs	https://doi.org/10.1016/j.checat.2021.10.003
State	Published - Oct 21 2021
Externally published	Yes

Access to Document

10.1016/j.checat.2021.10.003

Cite this

@article{53b4b68e043945e8880b1d329175da99,

title = "Chloride-mediated electrochemical synthesis of oxazolines",

abstract = "In this issue of Chem Catalysis, Liang et al. report an efficient electrochemical cyclization reaction of alkenes and amides to produce oxazolines with broad substrate scopes and good selectivities. A chloronium species generated by the chloride-mediated redox catalysis is proposed as a key intermediate.",

author = "Wenda Wu and Gang Li and Liu, \{T. Leo\}",

note = "Publisher Copyright: {\textcopyright} 2021",

year = "2021",

month = oct,

day = "21",

doi = "10.1016/j.checat.2021.10.003",

language = "English",

volume = "1",

pages = "966--967",

journal = "Chem Catalysis",

issn = "2667-1107",

publisher = "Cell Press",

number = "5",

}

TY - JOUR

T1 - Chloride-mediated electrochemical synthesis of oxazolines

AU - Wu, Wenda

AU - Li, Gang

AU - Liu, T. Leo

PY - 2021/10/21

Y1 - 2021/10/21

N2 - In this issue of Chem Catalysis, Liang et al. report an efficient electrochemical cyclization reaction of alkenes and amides to produce oxazolines with broad substrate scopes and good selectivities. A chloronium species generated by the chloride-mediated redox catalysis is proposed as a key intermediate.

AB - In this issue of Chem Catalysis, Liang et al. report an efficient electrochemical cyclization reaction of alkenes and amides to produce oxazolines with broad substrate scopes and good selectivities. A chloronium species generated by the chloride-mediated redox catalysis is proposed as a key intermediate.

UR - https://www.scopus.com/pages/publications/85126078233

U2 - 10.1016/j.checat.2021.10.003

DO - 10.1016/j.checat.2021.10.003

M3 - Comment/debate

AN - SCOPUS:85126078233

SN - 2667-1107

VL - 1

SP - 966

EP - 967

JO - Chem Catalysis

JF - Chem Catalysis

IS - 5

ER -

Chloride-mediated electrochemical synthesis of oxazolines

Abstract

Access to Document

Other files and links

Fingerprint

Cite this