Efficient and selective cleavage of t-butoxycarbonyl group from carbamates and amides by CeCl3·7H2O-NaI

Yadav, J. S. ; Subba Reddy, B. V. ; Srinivasa Reddy, K. (2002) Efficient and selective cleavage of t-butoxycarbonyl group from carbamates and amides by CeCl3·7H2O-NaI Synlett, 2002 (3). 0468-0470. ISSN 0936-5214

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Official URL: http://www.thieme-connect.com/ejournals/abstract/s...

Related URL: http://dx.doi.org/10.1055/s-2002-20467

Abstract

A highly selective cleavage of the t-butoxycarbonyl group has been achieved in high yields using CeCl3·7H2O-NaI in acetonitrile at ambient temperature under neutral conditions. This method is mild and compatible with a wide range of functional groups such as THP, TBDMS, TBDPS, trityl ethers, mono-BOC or Cbz protected amines, acetamide, sulfonamide and benzamide etc., present in the substrate.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Cerium Reagents; Carbamates; Amides; α-amino Acids
ID Code:62856
Deposited On:24 Sep 2011 04:41
Last Modified:24 Sep 2011 04:41

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