Abstract
Stereoselective functionalization of the 1'-position of 4'-thionucleosides was achieved using a stereoselective S(N)2 reaction controlled by 5-membered ring coordination.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenosine A3 Receptor Antagonists
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Drug Design
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Humans
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Hydrogen Bonding
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Stereoisomerism
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Thionucleosides / chemical synthesis*
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Thionucleosides / chemistry
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Thionucleosides / pharmacology
Substances
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Adenosine A3 Receptor Antagonists
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Thionucleosides