Syntheses of penta-O-benzyl-myo-inositols, O-β-L-arabinosyl-(1→2)-sn-myo-inositol, O-α-D-galactosyl-(1→3)-sn-myo-inositol, and O-α-D-galactosyl-(1→6)-O-α-D-galactosyl-(1→3)-sn-myo-inositol

被引：12

作者：

Koto, S ^{[1
]}

Hirooka, M

Yoshida, T

Takenaka, K

Asai, C

Nagamitsu, T

Sakuma, H

Sakurai, M

Masuzawa, S

Komiya, M

Sato, T

Zen, S

Yago, K

Tomonaga, F

机构：

[1] Kitasato Univ, Sch Pharmaceut Sci, Minato Ku, Tokyo 1088641, Japan

[2] Kitasato Univ Hosp, Dept Pharm, Sagamihara, Kanagawa 2288555, Japan

来源：

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN | 2000年 / 73卷 / 11期

关键词：

D O I：

10.1246/bcsj.73.2521

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Two-step conversions of myo-inositol into (+/-)-2,3,4,5,6- and 1,3,4,5,6-penta-0-benzyl-myo-inositols are described. Starting from these monohydroxy derivatives of myo-inositol, O-beta -L-arabinopyranosyl-(1-->2)-sn-myo-inositol from Japanese green tea [], Camellia sinensis, and O-alpha -D-galactopyranosyl-(1-->3)-sn-myo-inositol (galactinol) as well as its homolog, O-alpha -D-galactopyranosy1-(1-->6(II))-galactinol, were synthesized by way of the in situ activating glycosylation procedure.(##)

引用

页码：2521 / 2529

页数：9

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