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Synthesis 2010(23): 4087-4095
DOI: 10.1055/s-0030-1258277
DOI: 10.1055/s-0030-1258277
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New YorkEfficient Synthesis of Naturally Occurring Skeleton 5-7-6 Tricyclic Pyrrolo[2,1-c][1,4]benzodiazepin-5-one and Its Derivatives via Cationic π-Cyclization [¹]
Further Information
Received
3 June 2010
Publication Date:
28 September 2010 (online)
Publication History
Publication Date:
28 September 2010 (online)

Abstract
An efficient method for the synthesis of a library based on the naturally occurring 5-7-6 tricyclic 5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one skeleton and its derivatives via cationic π-(7-endo) cyclization is described.
Key words
pyrrole - antibiotics - π-cyclization - oxidation - reduction
- Supporting Information for this article is available online:
- Supporting Information
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CDRI communication no. 7931.