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Synlett 2006(20): 3403-3406
DOI: 10.1055/s-2006-958427
DOI: 10.1055/s-2006-958427
LETTER
© Georg Thieme Verlag Stuttgart · New York
Diastereoselectivity in the Synthesis of syn-cis-3a-Hydroxypyrrolo[2,3-b]indoline N α ′-Methyl-dipeptide Methyl Esters
Further Information
Received
14 June 2006
Publication Date:
08 December 2006 (online)
Publication History
Publication Date:
08 December 2006 (online)
![](https://www.thieme-connect.de/media/synlett/200620/lookinside/thumbnails/10.1055-s-2006-958427-1.jpg)
Abstract
Described herein is a high yielding, diastereoselective synthesis of the syn-cis hydroxypyrroloindoline moiety by oxidation of the N α-trityl-tryptophan-N α ′-methyl-dipeptide methyl esters.
Key words
hydroxypyrroloindole - peptide natural products - oxidation - diastereoselectivity
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