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Protecting Group Control of Hydroxyketone-Hemiketal Tautomeric Equilibrium Enables the Stereoselective Synthesis of a 1′-Azido C-Nucleoside
Subhankar Panda
, Moyosore O. Orimoloye
, Tej Narayan Poudel
, Steven De Jonghe
, Dirk Jochmans
, Johan Neyts
,
Courtney C. Aldrich
Medicinal Chemistry
Research output
:
Contribution to journal
›
Article
›
peer-review
1
Scopus citations
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Dive into the research topics of 'Protecting Group Control of Hydroxyketone-Hemiketal Tautomeric Equilibrium Enables the Stereoselective Synthesis of a 1′-Azido C-Nucleoside'. Together they form a unique fingerprint.
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Keyphrases
Protecting Groups
100%
Azido
100%
Group Control
100%
Stereoselective Synthesis
100%
Tautomeric Equilibrium
100%
α-Hydroxy Ketones
100%
C-nucleosides
100%
Hemiketal
100%
Nucleosides
66%
Azidation
66%
Antiviral Drugs
33%
Azides
33%
Diastereoselectivity
33%
Lewis Acids
33%
Bioorthogonal
33%
Tetrazole
33%
Acid-promoted
33%
Conformational Control
33%
Schmidt Reaction
33%
Ring-chain tautomerism
33%
Chemistry
Stereoselective Synthesis
100%
C-Nucleoside
100%
Hemiketal
100%
Protecting Groups
100%
Nucleoside
66%
Azide
33%
Diastereoselectivity
33%
Tautomer
33%
Tautomerization
33%
Schmidt Reaction
33%
Lewis Acid
33%
formation
33%
Tetrazole
33%