CARBOHYDRATE SYNTHESIS FOR NUCLEAR-MEDICINE - A NEW, RAPID, AND STEREOSPECIFIC ROUTE TO 2-DEOXY-2-FLUORO-D-GLUCOSE

被引：36

作者：

DESSINGES, A ^{[1
]}

OLESKER, A ^{[1
]}

LUKACS, G ^{[1
]}

THANG, TT ^{[1
]}

机构：

[1] UNIV MONTPELLIER 2,CNRS,ERA 948,F-34060 MONTPELLIER,FRANCE

来源：

CARBOHYDRATE RESEARCH | 1984年 / 126卷 / 01期

关键词：

D O I：

10.1016/0008-6215(84)85137-X

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：C6 / C8

页数：3

共 15 条

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[6] GOODMAN MM, 1981, RADIOPHARMACEUTICALS, P801
[7] FLUORINATION WITH F2 - CONVENIENT SYNTHESIS OF 2-DEOXY-2-FLUORO-D-GLUCOSE
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[9] DIRECT DISPLACEMENT WITH ANHYDROUS FLUORIDE OF THE C-2 TRIFLUOROMETHANESULFONATE OF METHYL 4,6-O-BENZYLIDENE-3-O-METHYL-2-O-TRIFLUOROMETHYLSULPHONYL-BETA-D-MANNOPYRANOSIDE
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[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1982, (17) : 972 - 973
[10] STERIC AND ELECTROSTATIC INTERACTIONS IN REACTIONS OF CARBOHYDRATES .3. DIRECT DISPLACEMENT OF C-2 SULFONATE OF METHYL 4,6-ORTHO-BENZYLIDENE-3-ORTHO-METHYL-2-ORTHO-METHYLSULFONYL-BETA-D-GLUCOPYRANOSIDES AND MANNOPYRANOSIDES
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