Study on the NBS-Induced Rearrangement of 2-tert-Prenyltryptamines

[摘要]：Treatment of 2-tert-prenyltryptamines with N-bromosuccinimide gives clean access to the marine natural product flustramine C and analogues with the tert-prenyl group shifted to the 3a-position of the resulting pyrrolo[2,3-b]indole (70-80%). Dihydroflustramine C was obtained by DIBAL-H reduction of flustramine C. Bromination or N-methylation of the indole moiety does not influence the course of the rearrangement.

[全文传递流程]：

一般上传文献全文的时限在1个工作日内