Novel synthetic equivalents of differentially protected tartaric aldehydes. A simple route to useful c-4 chiral synthons

Dhavale, Dilip D. ; Tagliavini, Emilio ; Trombini, Claudio ; Umani-Ronchi, Achille (1988) Novel synthetic equivalents of differentially protected tartaric aldehydes. A simple route to useful c-4 chiral synthons Tetrahedron Letters, 29 (47). pp. 6163-6165. 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)82295-9

Abstract

The synthesis of 4-acetoxy-3-O-benzyl-1,2-O-isopropylidene aldotetroses from D-glucose is reported. These synthetic equivalents of tartaric aldehydes are chemoselectively reduced at the acetoxylated center leading to a series of useful differentially protected C-4 chiral synthons.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:9566
Deposited On:02 Nov 2010 11:55
Last Modified:01 Jun 2011 10:37

Repository Staff Only: item control page