Journal
ORGANIC LETTERS
Volume 19, Issue 19, Pages 5022-5025Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b02005
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- BRNS, Mumbai
- Council of Scientific and Industrial Research (CSIR), New Delhi
- SERB, New Delhi
- IRCC, IIT Bombay
- CSIR, New Delhi
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An efficient protocol for the synthesis of pyrrolo[1,2-a]indole derivatives having sulfide functionality using cascade radical cyclization on propargylindole is described. The nature of the substituents at the propargylic carbon bearing nitrogen of the indole has a profound effect on the rate, yield, and nature of the product obtained by the cascade radical cyclization. An expeditious one-pot route for cascade radical cyclization-desulfurization is also presented. Products obtained were elaborated to the core of the putative structure of the yuremamine and indoline derivative with five contiguous stereocenters.
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