Microwave-assisted regioselective synthesis of acyclic nucleosides through an alkylating reaction with 2-oxa-1,4-butanediol diacetate

Canadian Journal of Chemistry

Volumn 84, Issue 5, 2006, Pages 819-824

  Qu, Guirong ^a   Han, Suhui ^a   Zhang, Zhiguang ^a   Geng, Mingwei ^a   Xue, Feng ^a  

^a HENAN NORMAL UNIVERSITY   (China)

Author keywords

2 oxa 1,4 butanediol diacetate; Acyclic nucleosides; Alkylation; Microwave irradiation; Regioselectivity

Indexed keywords

ALKYLATION; CATALYSTS; REACTION KINETICS; SOLVENTS; SYNTHESIS (CHEMICAL);

2-OXA-1,4-BUTANEDIOL DIACETATE; ACYCLIC NUCLEOSIDES; MICROWAVE IRRADIATION; REGIOSELECTIVITY;

NUCLEIC ACIDS;

2 OXA 1,4 BUTANEDIOL DIACETATE; 9 [(2 ACETOXYETHOXY)METHYL 6 (P TOLYLAMINO)PURINE; 9 [(2 ACETOXYETHOXY)METHYL] 2 AMINO 6 (P TOLYLAMINO) PURINE; 9 [(2 ACETOXYETHOXY)METHYL] 2 CHLORO 6 (P METHOXY PHENYLAMINO)PURINE; 9 [(2 ACETOXYETHOXY)METHYL] 2 CHLORO 6 (P TOLYLAMINO) PURINE; 9 [(2 ACETOXYETHOXY)METHYL] 2 CHLORO 6 CYCLOHEXYLAMINO PURINE; 9 [(2 ACETOXYETHOXY)METHYL] 2 CHLORO 6 PHENYLAMINO PURINE; 9 [(2 ACETOXYETHOXY)METHYL] 6 (P ETHOXYPHENYLAMINO) PURINE; 9 [(2 ACETOXYETHOXY)METHYL] 6 (P METHOXYPHENYL AMINO)PURINE; 9 [(2 ACETOXYETHOXY)METHYL] 6 CHLOROPURINE; 9 [(2 ACETOXYETHOXY)METHYL] 6 CYCLOHEXYLAMINOPURINE; 9 [(2 ACETOXYETHOXY)METHYL] 6 PHENYLAMINOPURINE; 9 [(ACETOXYETHOXY)METHYL]HYPOXANTHINE; ACICLOVIR; ACYCLIC NUCLEOSIDE; GANCICLOVIR; PENCICLOVIR; PURINE; SOLVENT; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CATALYST; DRUG STRUCTURE; ENVIRONMENTAL FACTOR; METHODOLOGY; MICROWAVE RADIATION; REACTION TIME; SYNTHESIS;

EID: 33747066349     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/V06-061     Document Type: Article

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