Author:
Lemieux R. U.,Watanabe K. A.,Pavia A. A.
Abstract
Both the anomers for methyl 2,3-dideoxy-D-glycero-pent-2-enofuranoside were characterized and hydrogenated to the corresponding methyl 2,3-dideoxy-D-glycero-pentofuranosides. The similar compounds were prepared in the pyranoside ring form but in the L-glycero configuration. The anomeric forms for methyl 3-deoxy-L-erythro-pentopyranoside are reported together with a number of their derivatives of interest for the study of solvation effects on conformational equilibria (21). The molar rotations of the deoxy and unsaturated glycosides are discussed as are the conformational properties of the various compounds.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
62 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献