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A Chiron Approach to Aminocytitols by Petasis-Borono-Mannich Reaction: Formal Synthesis of (+)-Conduramine E and (-)-Conduramine E

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field Value
 
Creator Ghosal, Partha
Shaw, A K
 
Date 2013-02-04T09:02:05Z
2013-02-04T09:02:05Z
2012
 
Identifier Journal of Organic Chemistry 2012, 77 (17), 7627–7632
http://hdl.handle.net/123456789/991
 
Description A chiron approach to stereoselective route for the synthesis of aminocytitols from carbohydrates is described. The formal synthesis of (+)-conduramine E and (-)-conduramine E was achieved by utilizing this strategy. The key features of the synthetic strategy include one pot three component Petasis-Borono-Mannich reaction to introduce the syn-ß-amino alcohol functionality of conduramine E and ring closing metathesis to construct its carbocyclic core. The present synthetic approach paves the way for stereoselective synthesis of several conduramines starting from carbohydrates
 
Format 886642 bytes
application/pdf
 
Language en
 
Relation CDRI Communication no. 8302
 
Subject Stereoselective
Carbohydrates
Aminocytitols
 
Title A Chiron Approach to Aminocytitols by Petasis-Borono-Mannich Reaction: Formal Synthesis of (+)-Conduramine E and (-)-Conduramine E
 
Type Article