PMID: 32672043DOI: 10.1021/acs.lett.0c02071Jul 17, 2020Paper
Stereoselective Synthesis of Vinylcyclopropa[b ]indolines via a Rh-Migration Strategy
Organic Letters
Pan GuoYaojia Jiang
Abstract
A mild rhodium catalytic system has been developed to synthesize vinylcyclopropa[b]indolines through cyclopropanation of indoles with vinyl carbenoids generated from ring opening of cyclopropenes in situ. By employing a Rh-migration strategy, the products can be obtained with good to excellent E:Z ratios (≤99:1) and complete diastereoselectivity (≤99:1). This method is easy, has a low catalyst loading, and works for a broad range of functionalities.
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