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Copper-catalyzed radical 1,2-cyclization of indoles with arylsulfonyl hydrazides: access to 2-thiolated 3H-pyrrolo[1,2-a]indoles
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2017-07-31 00:00:00 , DOI: 10.1039/c7qo00478h
Jiawei Zhu 1, 2, 3, 4, 5 , Song Sun 1, 2, 3, 4, 5 , Minfang Xia 1, 2, 3, 4, 5 , Ning Gu 1, 2, 3, 4, 5 , Jiang Cheng 1, 2, 3, 4, 5
Affiliation  

A copper-catalyzed cascade radical 1,2-cyclization of indoles with arylsulfonyl hydrazides was developed, affording a series of 2-thiolated 3H-pyrrolo[1,2-a]indoles in moderate to excellent yields. This transformation proceeded with sequential radical addition to a triple bond and a cyclization procedure, where arylsulfonyl hydrazides served as thioarylation reagents.

中文翻译:

铜催化的芳基磺酰肼与吲哚的自由基1,2-环化反应:获得2-硫代3 H-吡咯并[1,2- a ]吲哚

开发了铜催化的芳基磺酰肼与吲哚的级联1,2-环化反应,以中等至极好的收率得到了一系列2-硫代3 H-吡咯并[1,2- a ]吲哚。该转化过程是依次将自由基加成至三键和环化程序,其中芳基磺酰肼用作硫代芳基化试剂。
更新日期:2017-10-25
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