SYNTHESIS AND RELATIVE CONFIGURATION OF THE SUGAR PART OF A MARINE TOXIN POLYCAVERNOSIDE-A

被引：16

作者：

FUJIWARA, K ^{[1
]}

AMANO, S ^{[1
]}

MURAI, A ^{[1
]}

机构：

[1] HOKKAIDO UNIV,FAC SCI,DEPT CHEM,SAPPORO,HOKKAIDO 060,JAPAN

来源：

CHEMISTRY LETTERS | 1995年 / 03期

关键词：

D O I：

10.1246/cl.1995.191

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Construction of the sugar part of polycavernoside-A, which has been isolated as one of toxic principles from the red alga Polycavernosa tsudai, is described starting from L-fucose and D-xylose in order to elucidate the relative stereochemistry.

引用

页码：191 / 192

页数：2

共 8 条

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OKA, T
MURAI, A
[J]. CHEMISTRY LETTERS, 1994, (11) : 2147 - 2150
[4] SYNTHESIS OF THE TETRAHYDROFURAN RING PART OF A MARINE TOXIN POLYCAVERNOSIDE-A
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FUJIWARA, K
MURAI, A
[J]. CHEMISTRY LETTERS, 1994, (11) : 2143 - 2146
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[6] AN EFFICIENT AND STEREOCONTROLLED SYNTHESIS OF THE NEPHRITOGENOSIDE CORE STRUCTURE
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[J]. TETRAHEDRON LETTERS, 1991, 32 (47) : 6873 - 6876
[7] IODONIUM ION PROMOTED REACTIONS AT THE ANOMERIC CENTER .2. AN EFFICIENT THIOGLYCOSIDE MEDIATED APPROACH TOWARD THE FORMATION OF 1,2-TRANS LINKED GLYCOSIDES AND GLYCOSIDIC ESTERS
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[J]. TETRAHEDRON LETTERS, 1990, 31 (09) : 1331 - 1334
[8] Yamashita M. Y., 1993, J AM CHEM SOC, V115, P1147

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