64880-43-9Relevant academic research and scientific papers
Synthesis of stereospecifically labeled 3,6-dideoxyhexoses.
Russell,Weigel,Han,Liu
, p. 95 - 114 (2007/10/02)
Preparations of ascarylose (3,6-dideoxy-L-arabino-hexose), abequose (3,6-dideoxy-D-xylo-hexose), and paratose (3,6-dideoxy-D-ribo-hexose) with stereospecific deuterium labeling at C-3 are discussed. The methods used to synthesize these sugars, such as the
Ring Opening of 2,3-, 3,4-, and 4,6-O-Benzylidene Acetals of Pyranosides by Photobromination with Bromotrichloromethane
Chana, Jasbir S.,Collins, Peter M.,Farnia, Farnoosh,Peacock, David J.
, p. 94 - 96 (2007/10/02)
2,3-, 3,4-, and 4,6-O-Benzylidene pyranoside dervatives on photobromination in bromotrichloromethane yield bromo-deoxy-pyranoside benzoates regio- and stereo-specifically which, for the acyl derivatives of the 2,3- and 3,4- acetals, is superior to their r
SYNTHESIS OF STEREOSPECIFICALLY LABELED CARBOHYDRATES: PREPARATION OF (3S)- AND (3R)-ASCARYLOSE
Han, Oksoo,Liu, Hung-wen
, p. 1073 - 1076 (2007/10/02)
The general problem of the synthesis of 3,6-dideoxy sugars containing stereospecifically labeled hydrogen isotope at C-3 is adressed for the specific case of ascarylose (3,6-dideoxy-L-arabino-hexose).
