PREPARATION OF 2-DEOXY, 3-DEOXY, AND 4-DEOXY DERIVATIVES OF L-RHAMNOSE, AND DERIVATIVES OF 2-AZIDO-2-DEOXY-L-RHAMNOSE AND 2,6-DIDEOXY-2-FLUORO-L-GLUCOSE, FOR USE IN GLYCOSYLATION REACTIONS

被引：15

作者：

BOLS, M ^{[1
]}

LUNDT, I ^{[1
]}

OTTOSEN, ER ^{[1
]}

机构：

[1] LEO PHARMACEUT PROD,DK-2750 BALLERUP,DENMARK

来源：

CARBOHYDRATE RESEARCH | 1991年 / 222卷

关键词：

D O I：

10.1016/0008-6215(91)89013-6

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：

The following compounds have been prepared for use as glycosyl donors: 1,3,4-tri-O-acetyl-2,6-dideoxy-2-fluoro-alpha,beta-L-glucopyranose (5a), 1,3,4-tri-O-acetyl-2,6-dideoxy-alpha,beta-L-arabino-hexopyranose (7a), 1,3,4-tri-O-acetyl-2-azido-2,6-dideoxy-alpha,beta-L-mannopyranose(8a), 1,2,4-tri-O-acetyl-3,6-dideoxy-alpha,L-arabino-hexopyranose (13a), and 1,2,3-tri-O-acetyl-4,6-dideoxy-alpha- (15a) and -beta-L-lyxo-hexopyranose (15b).

引用

收藏

页码：141 / 149

页数：9

相关论文

共 15 条

[1] PREPARATION OF 3-DEOXY-ALDONOLACTONES BY HYDROGENOLYSIS OF ACETYLATED ALDONOLACTONES [J].

BOCK, K ;

LUNDT, I ;

PEDERSEN, C .

ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1981, 35 (03) :155-162

[2] AMINO-ACIDS AND AMINO-SUGARS FROM BROMODEOXYALDONOLACTONES .8. [J].

BOCK, K ;

LUNDT, I ;

PEDERSEN, C .

ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1987, 41 (06) :435-441

[3] REACTION OF ALDONIC ACIDS WITH HYDROGEN BROMIDE .2. THE PREPARATION OF SOME BROMODEOXY-HEXOSES AND DEOXY-HEXOSES FROM BROMODEOXYALDONIC ACIDS [J].

BOCK, K ;

LUNDT, I ;

PEDERSEN, C .

CARBOHYDRATE RESEARCH, 1981, 90 (01) :7-16

[4] PREPARATION OF 2,3-EPOXYALDONOLACTONES AND THEIR CONVERSION INTO 2-FLUORO-2-DEOXY-ALDONOLACTONES AND 2-FLUORO-2-DEOXY-SUGARS [J].

BOLS, M ;

LUNDT, I .

ACTA CHEMICA SCANDINAVICA, 1990, 44 (03) :252-256

[5] FLUOROCARBOHYDRATES .28. SYNTHESIS AND CHARACTERIZATION OF 2-DEOXY-2-FLUORO-DERIVATIVES OF L-RHAMNOSE AND L-EPIRHAMNOSE [J].

BUTCHARD, GC ;

KENT, PW .

TETRAHEDRON, 1979, 35 (20) :2439-2443

[6] SYNTHESIS AND CYTOTOXIC ACTIVITY OF 1,3,4-TRI-O-ACETYL-2,6-DIDEOXY-L-ARABINO-HEXOPYRANOSE AND 1,3,4-TRI-O-ACETYL-2,6-DIDEOXY-L-LYXO-HEXOPYRANOSE [J].

HADFIELD, AF ;

CUNNINGHAM, L ;

SARTORELLI, AC .

CARBOHYDRATE RESEARCH, 1979, 72 (JUL) :93-104

[7]

Isbell HS, 1933, BUR STAND J RES, V11, P649

[8]

ISELIN B, 1933, HELV CHIM ACTA, V11, P649

[9] LACTONES .15. SYNTHESIS OF 4,6-DIDEOXY-L-LYXO-HEXOPYRANOSE AND 4,6-DIDEOXY-L-LYXO-HEXONOLACTONE [J].

KEFURT, K ;

KEFURTOV.Z ;

JARY, J .

COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 1971, 36 (04) :1701-&

[10]

LUNDT I, UNPUB