A short formal synthesis of (-)-serricornine

Article abstract of DOI:10.1080/00397919408013822

A short and efficient formal synthesis of serricornine (1), the sex pheromone of Lasioderma serricorne F., is described. The homochiral aldol 5 is straightforwardly converted to tosylate 9 to give homochiral lactone 2a (6 steps. 22% overall yield from oxazolidinone 4), a known precursor of (-)-1.

Full text of DOI:10.1080/00397919408013822

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Short Formal Synthesis of (-)-
Serricornine
Ronaldo A. Pilli a & Carlos K. Z. De Andrade a
a Universidade Estadual de Campinas, Instituto de
Química , 13081-970, Campinas, SP Brazil
Published online: 23 Sep 2006.
To cite this article: Ronaldo A. Pilli & Carlos K. Z. De Andrade (1994) A Short Formal
Synthesis of (-)-Serricornine, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 24:2, 233-241, DOI:
10.1080/00397919408013822
To link to this article: http://dx.doi.org/10.1080/00397919408013822
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