400. Deoxy-sugars. Part V. A reinvestigation of the glycal method for the synthesis of 2-deoxy-D- and -L-ribose
β Scribed by Deriaz, R. E. ;Overend, W. G. ;Stacey, M. ;Teece, Ethel G. ;Wiggins, L. F.
- Book ID
- 120579087
- Publisher
- The Royal Society of Chemistry
- Year
- 1949
- Weight
- 650 KB
- Category
- Article
- ISSN
- 0368-1769
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π SIMILAR VOLUMES
## For introducing 14C into position I of 2-deoxyaldoses, methods based on prolongation of the carbon chain usually come into consideration since one can proceed from simple and inexpensive 14C-compounds. Such a possibility is ofleered by the method of Fisher and Sowden'l? 2, which was applied by
Considerable effort has been devoted over the years to the synthesis of amino nucleosides spurred on largely by the antibiotic properties exhibited by many of them. l-4 However, the synthesis of 2'-amino-2'-deoxy nucleosides which have the amino group in the "up" (arabino) configuration has proved r