HIGHLY STEREOSELECTIVE GLYCOSYLATION OF SIALIC-ACID AIDED BY STEREOCONTROLLING AUXILIARIES

被引：102

作者：

ITO, Y ^{[1
]}

OGAWA, T ^{[1
]}

机构：

[1] INST PHYS & CHEM RES,WAKO,SAITAMA 35101,JAPAN

来源：

TETRAHEDRON | 1990年 / 46卷 / 01期

关键词：

D O I：

10.1016/S0040-4020(01)97586-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：89 / 102

页数：14

共 38 条

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[6] AN EFFICIENT APPROACH TO STEREOSELECTIVE GLYCOSYLATION OF N-ACETYLNEURAMINIC ACID - USE OF PHENYLSELENYL GROUP AS A STEREOCONTROLLING AUXILIARY
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[7] HIGHLY STEREOSELECTIVE GLYCOSYLATION OF N-ACETYLNEURAMINIC ACID AIDED BY A PHENYLTHIO SUBSTITUENT AS A STEREOCONTROLLING AUXILIARY
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[8] NOVEL APPROACHES TO GLYCOSIDE SYNTHESIS - SULFENATE ESTERS AS GLYCOSYL ACCEPTORS - A NOVEL-APPROACH TO THE SYNTHESIS OF 2-DEOXYGLYCOSIDES
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[J]. TETRAHEDRON LETTERS, 1987, 28 (24) : 2723 - 2726
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