SYNTHETIC STUDY TOWARD VINEOMYCINS - SYNTHESIS OF C-ARYL GLYCOSIDE SECTOR VIA CP2HFCL2-AGCLO4-PROMOTED TACTICS

被引：67

作者：

MATSUMOTO, T ^{[1
]}

KATSUKI, M ^{[1
]}

JONA, H ^{[1
]}

SUZUKI, K ^{[1
]}

机构：

[1] KEIO UNIV,DEPT CHEM,YOKOHAMA,KANAGAWA 223,JAPAN

来源：

TETRAHEDRON LETTERS | 1989年 / 30卷 / 45期

关键词：

D O I：

10.1016/S0040-4039(01)93337-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：6185 / 6188

页数：4

共 15 条

[1] TOTAL SYNTHESIS OF VINEOMYCINONE-B2 METHYL-ESTER
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[2] SIMPLE SYNTHESIS OF GLYCOSYL FLUORIDES
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[J]. CHEMISTRY LETTERS, 1984, (10) : 1747 - 1750
[3] THE STRUCTURE OF VINEOMYCIN-B-2
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OMURA, S
[J]. JOURNAL OF ANTIBIOTICS, 1981, 34 (11) : 1517 - 1518
[4] SYNTHESIS OF RAC-FRIDAMYCIN-E AND ENT-FRIDAMYCIN-E
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BALTUS, W
[J]. TETRAHEDRON, 1988, 44 (01) : 49 - 54
[5] NEW GLYCOSIDATION REACTION .1. COMBINATIONAL USE OF CP2ZRCL2-AGCLO4 FOR ACTIVATION OF GLYCOSYL FLUORIDES AND APPLICATION TO HIGHLY BETA-SELECTIVE GLYCOSIDATION OF D-MYCINOSE
MATSUMOTO, T
MAETA, H
SUZUKI, K
TSUCHIHASHI, G
[J]. TETRAHEDRON LETTERS, 1988, 29 (29) : 3567 - 3570
[6] NEW APPROACH TO C-ARYL GLYCOSIDES STARTING FROM PHENOL AND GLYCOSYL FLUORIDE - LEWIS ACID-CATALYZED REARRANGEMENT OF O-GLYCOSIDE TO C-GLYCOSIDE
MATSUMOTO, T
KATSUKI, M
SUZUKI, K
[J]. TETRAHEDRON LETTERS, 1988, 29 (52) : 6935 - 6938
[7] CP2ZRCL2-AGCLO4 - EFFICIENT PROMOTER FOR THE FRIEDEL-CRAFTS APPROACH TO C-ARYL GLYCOSIDES
MATSUMOTO, T
KATSUKI, M
SUZUKI, K
[J]. TETRAHEDRON LETTERS, 1989, 30 (07) : 833 - 836
[8] 1ST TOTAL SYNTHESIS OF MYCINAMICIN-IV AND MYCINAMICIN-VII SUCCESSFUL APPLICATION OF NEW GLYCOSIDATION REACTION
MATSUMOTO, T
MAETA, H
SUZUKI, K
TSUCHIHASHI, G
[J]. TETRAHEDRON LETTERS, 1988, 29 (29) : 3575 - 3578
[9] MATSUMOTO T, 1988, TETRAHEDRON LETT, V29, P3571
[10] ISOLATION AND STRUCTURE ELUCIDATION OF SOME COMPONENTS OF THE ANTITUMOR ANTIBIOTIC MIXTURE RUBIFLAVIN
NADIG, H
SEQUIN, U
[J]. HELVETICA CHIMICA ACTA, 1987, 70 (04) : 1217 - 1228

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