CHEMICAL MODIFICATION OF LACTOSE .6. STUDIES ON REACTIVITIES OF SECONDARY HYDROXYL-GROUPS IN 1,6-ANHYDRO-4',6'-0-BENZYLIDENE-BETA-LACTOSE BY SELECTIVE BENZOYLATION

被引：17

作者：

CHIBA, T ^{[1
]}

HAGA, M ^{[1
]}

TEJIMA, S ^{[1
]}

机构：

[1] NAGOYA CITY UNIV,FAC PHARM SCI,NAGOYA,JAPAN

来源：

CARBOHYDRATE RESEARCH | 1975年 / 45卷 / DEC期

关键词：

D O I：

10.1016/S0008-6215(00)85861-9

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：

引用

页码：11 / 18

页数：8

共 18 条

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HOUGH, L ;

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[2]

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[3]

CHIBA T, 1974, CHEM PHARM BULL, V22, P398

[4]

DEFERRARI JO, 1972, METHODS CARBOHYD CHE, V6, P365

[5]

HIRST EL, 1963, METHODS CARBOHYDR CH, V2, P147

[6] A PROPOSED INVERSION MECHANISM FOR THE FORMATION OF LEVOGLUCOSAN FROM PHENYL BETA-D-GLUCOSIDE AND TRIMETHYLGLUCOSYLAMMONIUM COMPOUNDS [J].

MCCLOSKEY, CM ;

COLEMAN, GH .

JOURNAL OF ORGANIC CHEMISTRY, 1945, 10 (03) :184-193

[7] Derivatives of 3 4-Monoacetone beta-1 6-Anhydrogalactose [J].

McCreath, D ;

Smith, F .

JOURNAL OF THE CHEMICAL SOCIETY, 1939, :387-391

[8]

MORI M, 1974, CHEM PHARM BULL, V22, P1331

[9]

MORI M, 1975, 95TH ANN M PHARM SOC

[10]

OKAMORI Y, 1973, CHEM PHARM BULL, V21, P2538

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