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  4. Diastereoselective synthesis of (1S,2S,3R,6S) 3-Chloro-3-methyl-6-isopropenyl-1,2-cyclohexanediol via Prins reaction induced by zinc and trimethylsilyl chloride

Diastereoselective synthesis of (1S,2S,3R,6S) 3-Chloro-3-methyl-6-isopropenyl-1,2-cyclohexanediol via Prins reaction induced by zinc and trimethylsilyl chloride

Author(s)
Marty, Maurus
Stoeckli-Evans, Helen  
Institut de chimie  
Neier, Reinhard  
Institut de chimie  
Date issued
1996
In
Tetrahedron, Elsevier, 1996/52/13/4645-4658
Abstract
While attempting to synthesize a potential inhibitor of the biosynthetic step of formation of PBG, a novel catalytic system inducing the Prins reaction was discovered. Treatment of epoxy geranial with Zn and trimethylsilyl chloride gave (1S,2S,3R,6S) 3-Chloro-3-methyl-6-isopropenyl-1,2-cyclohexanediol in high diastereoselectivity.
Publication type
journal article
Identifiers
https://libra.unine.ch/handle/20.500.14713/58077
DOI
10.1016/0040-4020(96)00167-6
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Marty_Maurus_-_Diastereoselective_synthesis_of_1S_2S_3R_6S_20070827.pdf

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