Selenium-controlled stereoselective synthesis of 2′-deoxynucleosides from glycals. A formal synthesis of AZT
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[1] S. Lalitha,et al. First chemical synthesis of deuterated 3′-azido-3′-deoxythymidine (AZT) , 1992 .
[2] C. Kim,et al. Facile, highly stereoselective synthesis of 2′,3′-dideoxy- and 2′,3′-didehydro-2′,3t'-dideoxy nucleosides via a furanoid glycal intermediate , 1992 .
[3] S. Ahn,et al. A highly stereoselective synthesis of anti-HIV 2',3'-dideoxy- and 2',3'-didehydro-2',3'-dideoxynucleosides , 1992 .
[4] D. Liotta,et al. Diastereoselective sulfenylation reactions employing N-phenylthio lactams under nonbasic conditions , 1992 .
[5] J. Chattopadhyaya,et al. SYNTHESIS OF NEW 2'-3'-MODIFIED URIDINE DERIVATIVES FROM 2',3'-ENE-2'-PHENYLSELENONYL URIDINE BY MICHAEL ADDITION REACTIONS , 1991 .
[6] H. Mitsuya,et al. Molecular targets for AIDS therapy. , 1990, Science.
[7] D. Liotta,et al. A general method for controlling glycosylation stereochemistry in the synthesis of 2'-deoxyribose nucleosides , 1990 .
[8] E. De Clercq,et al. 3'-substituted 2',3'-dideoxynucleoside analogues as potential anti-HIV (HTLV-III/LAV) agents. , 1987, Journal of medicinal chemistry.
[9] J. Horwitz,et al. Nucleosides. V. The Monomesylates of 1-(2'-Deoxy-β-D-lyxofuranosyl)thymine1,2 , 1964 .