NUCLEOSIDE ANALOGS . SYNTHESIS OF 6-(6- AMINO-9-PURINYL)-1,5-ANHYDRO-6-DEOXY-L-ALLITOL

被引：13

作者：

VINCE, R

DONOVAN, J

机构：

[1] Department of Medicinal Chemistry, College of Pharmacy, University of Minnesota, Minneapolis

[2] Department of Pharmaceutical Chemistry, School of Pharmacy, University of Mississippi, University

来源：

JOURNAL OF MEDICINAL CHEMISTRY | 1969年 / 12卷 / 01期

关键词：

D O I：

10.1021/jm00301a049

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

[No abstract available]

引用

页码：175 / &

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CHARGAFF E, 1960, NUCLEIC ACIDS, V3, P304

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[6] STUDIES OF SYNTHESIS AND CONFORMATION IN D-RIBOPYRANOSE SERIES [J].

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[7]

HANDSCHUMACHER RE, 1960, NUCLEIC ACIDS, V3, P453

[8]

ROLL PM, 1956, J BIOL CHEM, V220, P439

[9] ENZYME INHIBITORS .8. STUDIES ON MODE OF BINDING OF SOME 6-SUBSTITUTED 9-(HYDROXYALKYL)PURINES TO ADENOSINE DEAMINASE [J].

SCHAEFFE.HJ ;

VOGEL, D ;

VINCE, R .

JOURNAL OF MEDICINAL CHEMISTRY, 1965, 8 (04) :502-&

[10] ENZYME INHIBITORS .I. INHIBITION OF ADENOSINE DEAMINASE BY ISOSTERIC NUCLEOSIDES [J].

SCHAEFFER, HJ ;

MARATHE, S ;

ALKS, V .

JOURNAL OF PHARMACEUTICAL SCIENCES, 1964, 53 (11) :1368-&

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