An expeditious approach for the synthesis of β-hydroxy aryl α-amino acids present in vancomycin

Rama Rao, A. V. ; Chakraborty, T. K. ; Laxma Reddy, K. ; Srinivasa Rao, A. (1994) An expeditious approach for the synthesis of β-hydroxy aryl α-amino acids present in vancomycin Tetrahedron Letters, 35 (28). pp. 5043-5046. ISSN 0040-4039

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

Related URL: http://dx.doi.org/10.1016/S0040-4039(00)73315-6

Abstract

Stereoselective synthesis of the β-hydroxyaryl amino acids which constitute C and E rings of vancomycin is described making use of benzylic oxidation and asymmetric dihydroxylation as the key steps.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Vancomycin; β-hydroxy Aryl Amino Acids; Diastereoselective Synthesis; Asymmetric Dihydroxylation
ID Code:20627
Deposited On:20 Nov 2010 13:50
Last Modified:20 May 2011 11:50

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