Cu-mediated selective N-arylation of aminotriazole acyclonucleosides

Helvetica Chimica Acta

Volumn 92, Issue 8, 2009, Pages 1503-1513

  Li, Wei ^a   Fan, Yuting ^a   Xia, Yi ^b   Rocchi, Palma ^c   Zhu, Ruizhi ^a   Qu, Fanqi ^a   Neyts, Johan ^d   Iovanna, Juan L ^c   Peng, Ling ^a,b  

^a WUHAN UNIVERSITY   (China)

^b AIX MARSEILLE UNIVERSITÉ   (France)

^c INSERM   (France)

^d REGA INSTITUTE FOR MEDICAL RESEARCH   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE FUNCTIONALITIES; AMIDE GROUPS; AMINE GROUPS; BORONIC ACID; CROSS COUPLING REACTIONS; N-ARYLATIONS; NUCLEOBASES;

AMINES; AROMATIC COMPOUNDS; BIOMOLECULES;

AMIDES;

ACYCLIC NUCLEOSIDE; AMIDE; AMINE; AMINOTRIAZOLE; ANTIVIRUS AGENT; BORONIC ACID DERIVATIVE; COPPER; NUCLEIC ACID BASE; PALLADIUM; REAGENT; RIBAVIRIN; TRIAZOLE DERIVATIVE;

ANTINEOPLASTIC ACTIVITY; ANTIVIRAL ACTIVITY; ARTICLE; ARYLATION; CANCER CELL CULTURE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; DRUG SYNTHESIS; HEPATITIS C VIRUS; HUMAN; HUMAN CELL; MASS SPECTROMETRY; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 69249221443     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200900033     Document Type: Article

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