Literature DB >> 24590818

Rhodium enalcarbenoids: direct synthesis of indoles by rhodium(II)-catalyzed [4+2] benzannulation of pyrroles.

Sudam Ganpat Dawande1, Vinaykumar Kanchupalli, Jagadeesh Kalepu, Haribabu Chennamsetti, Bapurao Sudam Lad, Sreenivas Katukojvala.   

Abstract

Disclosed herein is the design of an unprecedented electrophilic rhodium enalcarbenoid which results from rhodium(II)-catalyzed decomposition of a new class of enaldiazo compounds. The synthetic utility of these enalcarbenoids has been successfully demonstrated in the first transition-metal-catalyzed [4+2] benzannulation of pyrroles, thus leading to substituted indoles. The new benzannulation has been applied to the efficient synthesis of the natural product leiocarpone as well as a potent adipocyte fatty-acid binding protein inhibitor.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  annulation; carbenes; diazo compounds; heterocycles; rhodium

Mesh:

Substances:

Year:  2014        PMID: 24590818     DOI: 10.1002/anie.201400161

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


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