Abstract
A novel and efficient synthesis of 4-substituted 2-oxazolidinones is described; the synthesis utilizes Sharpless asymmetric dihydroxylation (AD) of appropriately substituted O-allylcarbamates and intramolecular cyclisation as key steps.
Keywords: chiral, substituted -oxazolidinones, asymmetric dihydroxylation, intramolecular cyclisation
Letters in Organic Chemistry
Title: A Simple Asymmetric Synthesis of 4-Substituted-2-Oxazolidinones
Volume: 2 Issue: 7
Author(s): V. J. Sattigeri, A. S.S.V. Srinivas, A. Soni, J. M. Khanna and A. Mehta
Affiliation:
Keywords: chiral, substituted -oxazolidinones, asymmetric dihydroxylation, intramolecular cyclisation
Abstract: A novel and efficient synthesis of 4-substituted 2-oxazolidinones is described; the synthesis utilizes Sharpless asymmetric dihydroxylation (AD) of appropriately substituted O-allylcarbamates and intramolecular cyclisation as key steps.
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Sattigeri J. V., Srinivas S.S.V. A., Soni A., Khanna M. J. and Mehta A., A Simple Asymmetric Synthesis of 4-Substituted-2-Oxazolidinones, Letters in Organic Chemistry 2005; 2 (7) . https://dx.doi.org/10.2174/157017805774296876
DOI https://dx.doi.org/10.2174/157017805774296876 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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