An efficient and stereoselective synthesis of (+)-α-cyperone

Article abstract of DOI:10.1080/00397919608003880

An efficient and stereoselective three step synthesis of (+)-α-cyperone 1 is described. The key step involves a stereoselective Michael addition of chiral imine to (R)-dihydrocarvone.

Full text of DOI:10.1080/00397919608003880

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Synthetic Communications:
An International Journal
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Synthetic Organic Chemistry
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An Efficient and
Stereoselective Synthesis of
(+)-α-Cyperone
Beatriz S.M. Tenius a , Adriana R. Rohde a
Mauricio M. Victor a & Cláudio Viegas Jr a
,
a Universidade Federal do Rio Grande do Sul,
Instituto de Química , 91501–970, Porto Alegre,
RS, Brazil
Published online: 21 Aug 2006.
To cite this article: Beatriz S.M. Tenius , Adriana R. Rohde , Mauricio M.
Victor & Cláudio Viegas Jr (1996) An Efficient and Stereoselective Synthesis
of (+)-α-Cyperone, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 26:1, 197-203, DOI:
10.1080/00397919608003880
To link to this article: http://dx.doi.org/10.1080/00397919608003880
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