Oxone-mediated oxidative carbon-heteroatom bond cleavage: Synthesis of benzoxazinones from benzoxazoles with α-oxocarboxylic acids

Hua Wang; Hua Yang; Yiping Li; Xin Hua Duan

doi:10.1039/c3ra47660j

Oxone-mediated oxidative carbon-heteroatom bond cleavage: Synthesis of benzoxazinones from benzoxazoles with α-oxocarboxylic acids

Hua Wang
, Hua Yang
, Yiping Li
, Xin Hua Duan

化学学院

Xi'an Jiaotong University

科研成果: 期刊稿件 › 文章 › 同行评审

26 引用（Scopus）

摘要

A metal-free oxidative cleavage of benzoxazoles using Oxone as an oxidant has been developed. The in situ formed o-aminophenol has been proved to react successfully with α-oxocarboxylic acids affording the benzoxazinones in moderate to good yields.

源语言	英语
页（从-至）	8720-8722
页数	3
期刊	RSC Advances
卷	4
期	17
DOI	https://doi.org/10.1039/c3ra47660j
出版状态	已出版 - 2014

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10.1039/c3ra47660j

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title = "Oxone-mediated oxidative carbon-heteroatom bond cleavage: Synthesis of benzoxazinones from benzoxazoles with α-oxocarboxylic acids",

abstract = "A metal-free oxidative cleavage of benzoxazoles using Oxone as an oxidant has been developed. The in situ formed o-aminophenol has been proved to react successfully with α-oxocarboxylic acids affording the benzoxazinones in moderate to good yields.",

author = "Hua Wang and Hua Yang and Yiping Li and Duan, \{Xin Hua\}",

year = "2014",

doi = "10.1039/c3ra47660j",

language = "英语",

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T1 - Oxone-mediated oxidative carbon-heteroatom bond cleavage

T2 - Synthesis of benzoxazinones from benzoxazoles with α-oxocarboxylic acids

AU - Wang, Hua

AU - Yang, Hua

AU - Li, Yiping

AU - Duan, Xin Hua

PY - 2014

Y1 - 2014

N2 - A metal-free oxidative cleavage of benzoxazoles using Oxone as an oxidant has been developed. The in situ formed o-aminophenol has been proved to react successfully with α-oxocarboxylic acids affording the benzoxazinones in moderate to good yields.

AB - A metal-free oxidative cleavage of benzoxazoles using Oxone as an oxidant has been developed. The in situ formed o-aminophenol has been proved to react successfully with α-oxocarboxylic acids affording the benzoxazinones in moderate to good yields.

UR - https://www.scopus.com/pages/publications/84893217518

U2 - 10.1039/c3ra47660j

DO - 10.1039/c3ra47660j

M3 - 文章

AN - SCOPUS:84893217518

SN - 2046-2069

VL - 4

SP - 8720

EP - 8722

JO - RSC Advances

JF - RSC Advances

IS - 17

ER -

Oxone-mediated oxidative carbon-heteroatom bond cleavage: Synthesis of benzoxazinones from benzoxazoles with α-oxocarboxylic acids

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