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Volumn 7, Issue 6, 2012, Pages 1044-1056

Synthesis, Anti-HIV Activity Studies, and insilico Rationalization of Cyclobutane-Fused Nucleosides

Author keywords

Antiviral agents; Carbocycles; HIV 1; Molecular modeling; Nucleosides

Indexed keywords

1 (1' CHLORO 4' HYDROXYMETHYL 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (1' FLUORO 4' HYDROXYMETHYL 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (4 HYDROXYMETHYL 3 OXABICYCLO[3.2.0]HEPT 6 EN 2 YL)THYMINE; 1 (4 TERT BUTYLDIMETHYLSILYLOXYMETHYL 3 OXABICYCLO[3.2.0]HEPT 6 EN 2 YL)THYMINE; 1 (4' HYDROXYMETHYL 6' HYDROXY 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (4' HYDROXYMETHYL 6' METHYLENE 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (4' HYDROXYMETHYL 6' OXO 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (4' TERT BUTYLDIMETHYLSILYLOXYMETHYL 1' CHLORO 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (4' TERT BUTYLDIMETHYLSILYLOXYMETHYL 1' FLUORO 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (4' TERT BUTYLDIMETHYLSILYLOXYMETHYL 6' METHYLENE 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (4' TERT BUTYLDIMETHYLSILYLOXYMETHYL 6' OXO 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (4' TERT BUTYLDIMETHYLSILYLOXYMETHYL 6',6' DIETHOXY 3' OXABICYCLO[3.2.0]HEPT 2 YL)THYMINE; 1 (HYDROXYMETHYL 3 OXABICYCLO[3.2.0]HEPT 6 EN 2 YL)THYMINE; 2 ACETYLOXY 4 TERT BUTYLDIMETHYLSILYLOXYMETHYL 6,6 DIETHOXY 3 OXABICYCLO[3.2.0]HEPTANE; 4 TERT BUTYLDIMETHYLSILYLOXYMETHYL 6,6 DIETHOXY 3 OXABICYCLO[3.2.0]HEPTAN 2 ONE; 4 TERT BUTYLDIMETHYLSILYLOXYMETHYL 7,7 DIETHOXY 3 OXABICYCLO[3.2.0]HEPTAN 2 ONE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; CYCLOBUTANE DERIVATIVE; NUCLEOSIDE ANALOG; RNA DIRECTED DNA POLYMERASE; STAVUDINE; UNCLASSIFIED DRUG;

EID: 84861556548     PISSN: 18607179     EISSN: 18607187     Source Type: Journal    
DOI: 10.1002/cmdc.201200059     Document Type: Article
Times cited : (8)

References (52)
  • 1
    • 73549088038 scopus 로고    scopus 로고
    • citations therein.
    • T. Cihlar, A. S. Ray, Antiviral Res. 2010, 85, 39-58 and citations therein.
    • (2010) Antiviral Res. , vol.85 , pp. 39-58
    • Cihlar, T.1    Ray, A.S.2
  • 25
    • 84861546577 scopus 로고    scopus 로고
    • All the attempts to carry out the photochemical reaction with the unprotected lactone failed.
    • All the attempts to carry out the photochemical reaction with the unprotected lactone failed.
  • 26
    • 84861549212 scopus 로고    scopus 로고
    • Addition of an asymmetrical olefin to an α,β-unsaturated lactone gives two regioisomers: the head-to-head (HH) and head-to-tail (HT) adducts, where head refers to the carbonyl end of the lactone and to the more substituted end of the olefin.
    • Addition of an asymmetrical olefin to an α, β-unsaturated lactone gives two regioisomers: the head-to-head (HH) and head-to-tail (HT) adducts, where head refers to the carbonyl end of the lactone and to the more substituted end of the olefin.
  • 35
    • 84861557504 scopus 로고    scopus 로고
    • The nucleoside numbering system is used to facilitate comparison of the synthesized nucleosides with regular nucleosides. The systematic numbering for these compounds is used in the Experimental Section.
    • The nucleoside numbering system is used to facilitate comparison of the synthesized nucleosides with regular nucleosides. The systematic numbering for these compounds is used in the Experimental Section.
  • 36
    • 84861557513 scopus 로고    scopus 로고
    • Marvin version5.4 (2010), ChemAxon Kft, Budapest (Hungary)
    • Marvin version5.4 (2010), ChemAxon Kft, Budapest (Hungary).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.