butoxycarbonyl-2-methylpropanoic acid (D) and (2R,6S)-7acetoxy-2,6-dimethyl-1-heptanol (G), by employing lipase-dodecyl propanoate (1 and 2), the components of the pheromone of Microdiprion pallipes, were synthesized from catalyzed kinetic resolution in a later step. two chiral and nonracemic buildi
✦ LIBER ✦
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
No coin nor oath required. For personal study only.
✦ 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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