CONVENIENT SYNTHESIS OF 2-FLUOROADENINE

被引：10

作者：

EATON, CN

DENNY, GH

机构：

[1] Merck Sharp & Dohme Research Laboratories, Division of Merck & Co., Inc., Rahway

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1969年 / 34卷 / 03期

关键词：

D O I：

10.1021/jo01255a062

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：747 / &

共 10 条

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[2] A NEW SYNTHESIS OF PURINE NUCLEOSIDES - THE SYNTHESIS OF ADENOSINE, GUANOSINE AND 2,6-DIAMINO-9-BETA-D-RIBOFURANOSYLPURINE [J].

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LOWY, BA .

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[3] 3'-DEOXYNUCLEOSIDES .V. 3'-DEOXY-2-FLUOROADENOSINE [J].

DICKINSON, MJ ;

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[4]

FORCHE E, 1962, METHODEN ORGANISCHEN, P215

[5] A CONVENIENT METHOD FOR SYNTHESIS OF 2-FLUOROADENOSINE [J].

MONTGOMERY, JA ;

HEWSON, K .

JOURNAL OF ORGANIC CHEMISTRY, 1968, 33 (01) :432-+

[6] SYNTHESIS OF POTENTIAL ANTICANCER AGENTS .20. 2-FLUOROPURINES [J].

MONTGOMERY, JA ;

HEWSON, K .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1960, 82 (02) :463-468

[7]

MONTGOMERY JA, 1965, PROGR DRUG RES, V8, P489

[8]

MONTGOMERY JA, 1968, MEDI26 AM CHEM SOC N

[9]

MONTGOMERY JA, 1965, PROGR DRUG RES, V8, P475

[10] METABOLISM OF 2-FLUOROADENOSINE BY EHRLICH ASCITES CELLS [J].

SHIGEURA, HT ;

BOXER, GE ;

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MELONI, ML .

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1965, 111 (03) :713-&

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