DSpace
 

DSpace at IIT Bombay >
IITB Publications >
Article >

Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/11351

Title: STEREOSELECTIVE TOTAL SYNTHESIS OF (2R,2'S,3Z)-1-0-(2-METHOXYHEXADECENYL)GLYCEROL AND (2R,2'S)-1-(2'-METHOXYHEXADECYL)GLYCEROL-POTENTIAL ANTITUMOR COMPOUNDS FROM SHARK LIVER OIL
Authors: BAIG, MHA
BASKARAN, S
BANERJEE, S
TRIVEDI, GK
Issue Date: 1995
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Citation: TETRAHEDRON, 51(16), 4723-4732
Abstract: A simple and high yielding route for the stereoselective synthesis of alkyl glycerol ethers namely (2R,2'S,3Z)-1-O-(2-methoxyhexadecenyl)glycerol 1 and (2R,2'S)-1-(2'-methoxyhexadecyl) glycerol 2, isolated form Shark liver oil is reported. The key reaction involves the Wittig olefination of the chiral aldehyde 12 with the ylide generated from tridecyl triphenyl phosphonium bromide results in the formation of compound 13, a precursor for the title compounds 1 and 2.
URI: http://dx.doi.org/10.1016/0040-4020(95)00156-3
http://dspace.library.iitb.ac.in/xmlui/handle/10054/11351
http://hdl.handle.net/10054/11351
ISSN: 0040-4020
Appears in Collections:Article

Files in This Item:

There are no files associated with this item.

View Statistics

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

Valid XHTML 1.0! DSpace Software Copyright © 2002-2010  Duraspace - Feedback