REACTIONS OF SUGAR CHLOROSULFATES: PART V. THE SYNTHESIS OF CHLORODEOXY SUGARS
作者:H. J. Jennings、J. K. N. Jones
DOI:10.1139/v65-319
日期:1965.8.1
The reaction of sulfuryl chloride with reducing sugars and their methyl glycopyranosides was shown to produce fully substituted pyranose derivatives containing both chlorodeoxy and chlorosulfate ester groups. It was demonstrated that the chlorodeoxy groups were formed by nucleophilic displacement (SN2) by chloride ion of specific reactive chlorosulfate groups in fully chlorosulfated intermediates.
THE REACTION OF SULPHURYL CHLORIDE WITH GLYCOSIDES AND SUGAR ALCOHOLS. PART I
作者:P. D. Bragg、J. K. N. Jones、J. C. Turner
DOI:10.1139/v59-207
日期:1959.9.1
The reaction of sulphurylchloride with methyl α-D-glucopyranoside, methyl 4,6-O-benzylidene-α-D-glucoside, methyl β-D-arabinopyranoside, D-mannitol, 2,5-O-methylene-D-mannitol, dulcitol, and sucro...