Enantioselective synthesis of ipsenol and ipsdienol using a (2-bromoallyl)borane derivative

Article abstract of DOI:10.1080/00397919708003047

(S)-(-)-Ipsenol and (S)-(+)-ipsdienol, a major component of the sex pheromone of the bark beetle, and their enantiomers were prepared enantioselectively using tartrate esters of (2-bromoallyl)boronic acid in the key step.

Full text of DOI:10.1080/00397919708003047

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Synthetic Communications: An
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Enantioselective Synthesis
of Ipsenol and Ipsdienol
Using a (2-Bromoallyl)borane
Derivative
Yasunori Yamamoto a , Shoji Hara a & Akira Suzuki a
a Division of Molecular Chemistry, Graduate School
of Engineering , Hokkaido University , Sapporo, 060,
Japan
Published online: 22 Aug 2006.
To cite this article: Yasunori Yamamoto , Shoji Hara & Akira Suzuki (1997)
Enantioselective Synthesis of Ipsenol and Ipsdienol Using a (2-Bromoallyl)borane
Derivative, Synthetic Communications: An International Journal for Rapid
Communication of Synthetic Organic Chemistry, 27:6, 1029-1036, DOI:
10.1080/00397919708003047
To link to this article: http://dx.doi.org/10.1080/00397919708003047
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