BARC/PUB/2002/0071

 
 

Synthesis of the 1,5-dimethylic chiron enantiomers, 3,7,11-trimethyldodec-10-en-1-ol: application to enantiomeric syntheses of tribolure and a marine fatty acid

 
     
 
Author(s)

Sankaranarayanan, S.; Sharma, A.; Chattopadhyay, S.
(BOD)

Source

Tetrahedron: Asymmetry, 2002. Vol. 13: pp. 1373-1378

ABSTRACT

A convenient synthesis of the title chiron antipodes has been developed starting from (±)-citronellol via a sequential acetylation protocol using two lipases. The different stereoisomers of the chiron were then functionalized by simple routes to (4R,8R)-dimethyldecanal, an insect pheromone and (5R,9R)-5,9,13-trimethyltetradecanoic acid, a marine phospholipid  fatty acid.

 
 
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