Abstract
THE synthesis of cyclitol glycosides is of interest because of the natural occurrence of these substances as such (galactinol) and as structural moieties of several antibiotics and phospholipids1,2. In this laboratory, attempts have been made to couple activated forms of glucose with protected derivatives3 of myo-inosamine-2 and, more recently, (+)-pinitol. The former efforts were unsuccessful; but the latter provided a glucoside (V) of pinitol in fair yield.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 52 print issues and online access
$199.00 per year
only $3.83 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to the full article PDF.
USD 39.95
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Reviewed by Angyal, S. J., and Anderson, L., Adv. Carbohydrate Chem., 14, 135 (1959).
Reviewed by Hawthorne, J. N., J. Lipid Res., 1, 255 (1960).
Drummond, G. I., and Anderson, L., J. Amer. Chem. Soc., 78, 1750 (1956).
Angyal, S. J., Macdonald, C. G., and Matheson, N. K., J. Chem. Soc., 3321 (1953).
Anderson, A. B., Tappi, 35, 198 (1952).
Jeanes, Allene, and Isbell, H. S., J. Res. Nat. Bur. Stand., 27, 125 (1941).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
CALDWELL, K., RAMAN, S. & ANDERSON, L. A Synthetic Cyclitol Glycoside. Nature 199, 373–374 (1963). https://doi.org/10.1038/199373b0
Issue date:
DOI: https://doi.org/10.1038/199373b0


