Pseudo-sugars. VII. Synthesis of pseudo-hexopyranose derivatives with .ALPHA.- and .BETA.-gluco configurations.
スポンサーリンク
概要
- 論文の詳細を見る
Several derivatives of pseudo-hexopyranose (5-hydroxymethyl-1,2,3,4-cyclohexanetetrol) with α-gluco, (1,2,4/3,5), and β-gluco, (1,3,5/2,4), configurations were synthesized starting from the compounds obtained by <I>cis</I>-hydroxylation and oxyamination of DL-di-<I>O</I>-acetyl-(1,3/2)-3-bromomethyl-5-cyclohexene-1,2-diol. The <SUP>1</SUP>H NMR chemical shifts of the acetyl methyl protons of the several acetyl derivatives of <I>N</I>-(<I>p</I>-tolylsulfonyl)-pseudoglucosamines are discussed.
- 公益社団法人 日本化学会の論文
著者
関連論文
- Ion Bernstein Wave Experiment on JFT-2M Tokamak
- ACETYLCHOLINE RECEPTOR-OPERATED INTRACELLULAR CALCIUM MOBILIZATION MODIFIED BY DIABETIC STATE IN SKELETAL MUSCLE
- Pseudo-sugars. VI. Synthesis of six isomers of 5-hydroxymethyl-1,2,3,4-cyclohexanetetrol (pseudo-hexopyranose) and their derivatives.
- Tetrodotoxin sensitivity of high K+-induced 86Rb efflux in the duodenal circular muscle of pigs.
- Pseudo-sugars. VII. Synthesis of pseudo-hexopyranose derivatives with .ALPHA.- and .BETA.-gluco configurations.