Highly stereoselective approach for β-hydroxy-α-amino acids from d-glucose: the synthesis of MeBmt

Rama Rao, A. V. ; Yadav, J. S. ; Chandrasekhar, S. ; Srinivas Rao, C. (1989) Highly stereoselective approach for β-hydroxy-α-amino acids from d-glucose: the synthesis of MeBmt Tetrahedron Letters, 30 (48). pp. 6769-6772. ISSN 0040-4039

Full text not available from this repository.

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

Related URL: http://dx.doi.org/10.1016/S0040-4039(00)70672-1

Abstract

A highly stereoselective protocol for the synthesis of β-hydroxy-α-amino acids from glucofuranose has been developed which has culminated in stereospecific synthesis of MeBmt- an unusual aminoacid component of immunosuppressive peptide cyclosporin.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:38922
Deposited On:05 May 2011 09:49
Last Modified:05 May 2011 09:49

Repository Staff Only: item control page