The Degradation of l-Arabinal to l-Erythrose1
GE Felton, W Freudenberg
Index: Felton; Freudenberg Journal of the American Chemical Society, 1935 , vol. 57, p. 1637,1638
Full Text: HTML
Citation Number: 5
Abstract
In a previous paper? it was shown that d-xylal by means of ozone could be degraded to a tetrose, which was identified as d-threose. Ozone apparently had a dualistic action. Firstly, it was added to the double bond, forming an unstable ozonide, which in turn was broken down under the influence of the solvent, acetic acid, to two aldehyde groups. Secondly, cleavage of the 1, 5-oxygen ring took place, a fact which had to be assumed since a free tetrose and ...
Related Articles:
Synthesis of acetobromo sugars
[Scheurer; Smith Journal of the American Chemical Society, 1954 , vol. 76, p. 3224]
Stereospecific synthesis of sugar-1-phosphates and their conversion to sugar nucleotides
[Timmons, Shannon C.; Jakeman, David L. Carbohydrate Research, 2008 , vol. 343, # 5 p. 865 - 874]
Cyclometalated gold (III) iminophosphoranes which incorporate carbohydrate groups
[Jarman, Bevan P.; Nicholson, Brian K. Journal of Organometallic Chemistry, 2012 , vol. 702, p. 1 - 9]