References
- Agrofoglio, L., Suhas, E., Farese, A., Condom, R., Challand, S., and Earl, R. A., Synthesis of carbocyclic nucleosides. Tetrahedron, 50, 10611-10670 (1994) https://doi.org/10.1016/S0040-4020(01)89258-9
- Borthwick, A. D. and Biggadike, K., Synthesis of chiral carbocyclic nucleoside. Tetrahedron, 48, 571-623 (1992) https://doi.org/10.1016/S0040-4020(01)88122-9
- Chatis, P. A. and Crumpacker, C. S., Resistance of herpesvirus to antiviral drugs. Antimicrob. Agents Chemother., 36, 1589-1595 (1992) https://doi.org/10.1128/AAC.36.8.1589
- Daiz, Y., Bravo, F., and Castillon, S., Synthesis of purine and pyrimidine isodideoxynucleosides from (S)-glycydol using iodoetherification as key step. synthesis of (S, S)-iso-ddA. J. Org. Chem., 64, 6508-6511 (1999) https://doi.org/10.1021/jo990495e
- Daluge, S. M., Good, S. S., Faletto, M. B., Miller, W. H., St Clair, M. H., Boone, L. R., Tisdale, M., Parry, N. R., Reardon, J. E., Dornsife, R. E., Averett, D. R., and Krenisky, T. A., 1592U89, A novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity. Antimicrob. Agents Chemother., 41, 1082-1093 (1997)
- Dias, E. L., Nguyun, S. T., and Grubbs, R. H., Well-defined Ruthenium olefin metathesis catalysts: Mechanism and activity. J. Am. Chem. Soc., 119, 3887-3897 (1997) https://doi.org/10.1021/ja963136z
- Herdewijn, P., De Clercq, E., Balzarini, J., and Vanderhaeghe, H., Synthesis and antiviral activity of the carbocyclic analogues of (E)-5-(2-halovinyl)-2'-deoxyuridine and (E)-5-(2-halovinyl)-2'-deoxycytidines. J. Med. Chem., 28, 550-555 (1985) https://doi.org/10.1021/jm50001a003
- Jenny, T. F., Horlacher, J., Previsani, N., and Benner, S., Carbocyclic analogs of nucleosides. Part 2. Synthesis of 2',3'-dideoxy-5'-homonucleoside analogs. Helv. Chim. Acta, 75, 1944-1954 (1992) https://doi.org/10.1002/hlca.19920750620
- Jeon, G. S. and Nair, V., New isomeric analogues of anti-HIV active azidonucleosides. Tetrahedron, 52, 12643-12650 (1996) https://doi.org/10.1016/0040-4020(96)00766-1
- Kitano, K., Miura, S., Ohrui, H., and Meguro, H., Synthesis of 4'-C-fluoromethylnucleosides as potential antineoplastic agents. Tetrahedron, 53, 13315-13322 (1997) https://doi.org/10.1016/S0040-4020(97)00844-2
- Ko, O. H. and Hong, J. H., Efficient synthesis of novel carbo-cyclic nucleosides via sequential Claisen rearrangement and ring-closing metathesis. Tetrahedron Lett., 43, 6399-6402 (2002) https://doi.org/10.1016/S0040-4039(02)01384-9
- Parker, W: B. and Cheng, Y. C., Mitochondrial toxicity of antiviral nucleoside analogues. J. NIH Res., 6, 57-61 (1994)
-
Schwab, P., Grubbs, R. H., and Ziller, J. W., Synthesis and application of
$RuCl_2(=CHR')(PR_3)_2$ : The influence of the alkylidene moiety on metathesis activity. J. Am. Chem. Soc., 118, 100-110 (1996) https://doi.org/10.1021/ja952676d - Roy, A. and Schneller, S. W., 4'-, 1'-Methyl SUbstituted 5'-norcarbanucleosides. J. Org. Chem., 68, 9269-9273 (2003) https://doi.org/10.1021/jo030238g
- Youssefyeh, R. D., Verheyden, J. H. P., and Moffatt, J. G., 4'-Substituted nucleosides. Hydroxymethylation of nucleoside 5'-aldehyde. J. Org. Chem., 44, 1301-1309 (1979) https://doi.org/10.1021/jo01322a024
- Wachmeister, J., Classon, B., and Samuelsson, B., Synthesis of 2' ,3'-dideoxycyclo-2'-pentenyl-3'-C-hydroxymethyl carbo-cyclic nucleoside analogues as potential anti-viral agents. Tetrahedron, 51, 2029-2038 (1995) https://doi.org/10.1016/0040-4020(94)01067-A