Synthesis, separation and NMR spectral analysis of methyl apiofuranosides

被引:72
作者
Ishii, T
Yanagisawa, M
机构
[1] Forestry & Forest Prod Res Inst, Tsukuba, Ibaraki 3058678, Japan
[2] Shimadzu Analyt & Measuring Ctr, Nakagyo Ku, Kyoto 604, Japan
关键词
apiose; 3-C-(hydroxymethyl)-D-glycero-aldotetrose; methyl apiofuranosides;
D O I
10.1016/S0008-6215(98)00262-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Methyl apiofuranosides were prepared by methanolysis of D-apiose. Four methyl apiofuranosides were separated by ion-exclusion and normal phase chromatography and their structures were characterized by H-1 and C-13 NMR spectroscopy. The composition of methyl apiofuranosides was almost the same as that of D-apiose in D2O. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:189 / 192
页数:4
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