A convenient one-step gingerol synthesis

Article abstract of DOI:10.1080/00397919908086182

Racemic 6-gingerol can be obtained in a one-pot reaction by hexanal addition to the dianion of zingerone at low temperature. Similarly, addition of octanal or decanal to the dianion provides 8-gingerol or 10-gingerol, respectively. Acid treatment of the gingerols allows for formation of the corresponding shogaols.

Full text of DOI:10.1080/00397919908086182

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Convenient One-Step
Gingerol Synthesis
a
a
Steven A. Fleming , Carrie W. Dyer & Julie
a
Eggington
a
Department of Chemistry and Biochemistry ,
Brigham Young University , Provo, Utah, 84602
Published online: 17 Sep 2007.
To cite this article: Steven A. Fleming , Carrie W. Dyer & Julie Eggington (1999) A
Convenient One-Step Gingerol Synthesis, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 29:11, 1933-1939,
DOI: 10.1080/00397919908086182
To link to this article: http://dx.doi.org/10.1080/00397919908086182
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