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

Author:

Chen Yan1,Song Weihong2,Han Xiaoyu1ORCID,Zhou Zhixiang1,Zhang Ziye1,Liu Kai1,Zeng Xiaofei2

Affiliation:

1. Zhejiang Provincial Key Laboratory for Chemical & Biological Processing Technology of Farm Products School of Biological & Chemical Engineering, Zhejiang University of Science and Technology

2. College of Material, Chemistry and Chemical Engineering, Hangzhou Normal University

Abstract

AbstractA 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.

Funder

Basic Public Welfare Research Program of Zhejiang Province

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Materials Science (miscellaneous),Biomaterials,Catalysis

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