Regiocontrolled C-8 acylation of castanospermine

Article abstract of DOI:10.1080/00397919608003581

A convenient route to previously unknown 8-acylated castanospermines is illustrated by synthesis of the butyryl derivative.

Full text of DOI:10.1080/00397919608003581

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Regiocontrolled C-8 Acylation
of Castanospermine
Nelson G. Landmesser a , Hon-Chung Tsui b , Chi-Hsin
R. King a & Leo A. Paquette b
a Hoechst Marion Roussel, Inc. , 2110 East Galbraith
Road, Cincinnati, Ohio, 45215
b Evans Chemical Laboratories, The Ohio State
University , Columbus, Ohio, 43210
Published online: 21 Aug 2006.
To cite this article: Nelson G. Landmesser , Hon-Chung Tsui , Chi-Hsin R. King & Leo
A. Paquette (1996) Regiocontrolled C-8 Acylation of Castanospermine, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:11, 2213-2221, DOI: 10.1080/00397919608003581
To link to this article: http://dx.doi.org/10.1080/00397919608003581
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