Highly Efficient Synthesis of 3,3-Disubstituted Oxindoles through Direct Oxidative Alkylarylation of N -Arylacrylamides with Simple Alkanes

IF 2 Q2 CHEMISTRY, ORGANIC
SynOpen Pub Date : 2023-01-26 DOI:10.1055/s-0042-1751451
Y. Chen, Weihong Song, Zhi Zhou, Ziye Zhang, Kai Liu, Xiaofei Zeng, Xiaoyu Han
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引用次数: 0

Abstract

A direct oxidative alkylarylation reaction of N-arylacrylamides with simple alkanes for the synthesis of 3,3-disubstituted oxindoles under metal-free conditions was demonstrated. By using PhI(OAc)2 [(diacetoxy)iodobenzene] as an oxidant, a series of 3,3-disubstituted oxindoles bearing different aryl or alkyl substituents were generated in moderate to excellent chemical yields via a radical-initiated alkylation/cyclization process. The reported method features good functional group tolerance and wide substrate range, and provides an effective method for the preparation of various alkyl substituted 3,3-disubstituted oxindoles.

Abstract Image

N -芳烯酰胺与简单烷烃直接氧化烷基化高效合成3,3-二取代氧吲哚
研究了n -芳基丙烯酰胺与简单烷烃在无金属条件下直接氧化烷基化合成3,3-二取代氧吲哚的反应。以PhI(OAc)2[(二乙酰氧基)碘苯]为氧化剂,通过自由基引发的烷基化/环化反应,生成了一系列含有不同芳基或烷基取代基的3,3-二取代氧吲哚,收率中等至优异。该方法具有官能团耐受性好、底物范围广的特点,为制备各种烷基取代3,3-二取代氧吲哚提供了一种有效的方法。
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来源期刊
SynOpen
SynOpen CHEMISTRY, ORGANIC-
CiteScore
2.30
自引率
4.00%
发文量
35
审稿时长
6 weeks
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