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Pheromone syntheses: A tropical approach. Enantioselective synthesis of the (2R,6S,10S) and (2S,6S,10S) isomers of methyl 2,6,10-trimethyldodecanoate

✍ Scribed by J.Tércio B. Ferreira; Paulo H.G. Zarbin


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
622 KB
Volume
4
Category
Article
ISSN
0968-0896

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✦ Synopsis


The enantioselective syntheses of two stereoisomers, (2R,6S,10S) and (2S,6S,10S), of methyl 2,6,10-trimethyldodecanote, out of eight possible isomers, are described , employing the stereoselective hydroboration of (-)-isopulegol (2) and (+)-neo-isopulegol (2a) as the key reaction.


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