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Enzyme Inhibitors. XIX. The Synthesis of Some l-Hydroxy-2-hydroxymethyl-4-(6-substituted-9-purinyl)cyclohexanes as Nucleoside Analogs
Howard J. Schaeffer,
Robert Vince
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Article
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peer-review
14
Scopus citations
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Dive into the research topics of 'Enzyme Inhibitors. XIX. The Synthesis of Some l-Hydroxy-2-hydroxymethyl-4-(6-substituted-9-purinyl)cyclohexanes as Nucleoside Analogs'. Together they form a unique fingerprint.
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Medicine & Life Sciences
Cyclohexanes
100%
Hydrogenation
78%
Enzyme Inhibitors
54%
Nucleosides
49%
Azides
44%
Ketones
39%
Amines
33%
lithium aluminum hydride
31%
Adenosine Deaminase Inhibitors
24%
Cyclohexane
24%
Cyclization
23%
Esters
16%
Alcohols
11%
Enzymes
8%
Chemical Compounds
Nucleoside Analogue
57%
Enzyme Inhibitor
54%
Cyclohexane
42%
Hydrogenation
34%
Azide
28%
Dieckmann Condensation
23%
Amine
20%
Adenosine
15%
Stereochemistry
13%
Displacement
12%
Cyclization Reaction
11%
Ester
9%
Alcohol
9%
Reduction
7%