참고문헌
- Stoeckler, J. D., Cambor, C. and Parks, R. E. Jr. : Human erythrocytic purine nucleoside phosphorylase : reaction with sugar-modified nucleoside substrate. Biochemistry 19, 102 (1980) https://doi.org/10.1021/bi00542a016
- Crimmins, M. T.: New development in the enantioselective synthesis of cyclopentyl carbcyclic nucleosides. Tetrahedron 54, 9229 (1998)
- Agrofoglio, L., Suhas, E., Farese, A., Condom, R., Challand, S. R., Earl, R. A. and Guedj, R. : Synthesis of carbocyclic nucleosides. Tetrahedron 50, 10611 (1994) https://doi.org/10.1016/S0040-4020(01)89258-9
- Borthwick, A. D. and Biggadike, K. : Synthesis of chiral carbocyclic nucleosides. Tetrahedron 48, 571 (1992) https://doi.org/10.1016/S0040-4020(01)88122-9
- Borcherding, D. R., Narayanan, S., Hasobe, M., McKee, J. G., Keller, B. T. and Borchardt, R. T. : Potential inhibitors of S-adenosylmethionine- dependent methyltransferases. II. Molecular dissections of neplanocin A as potential inhibitors of S-adenosylhomocysteine hydrolase. J. Med. Chem. 31, 1729 (1988)
- Marquez, V. E., Lim, M.-I., Treanor, S. P., Plowman, J., Priest, M. A., Markovac, A., Khan, M.'S., Kaskar, B. and Driscoll, J. S. : Cyclopentenylcytosine. A carbocyclic nucleoside with antitumor and antiviral properties. J. Med. Chem. 31, 1687 (1988)
- Phadtare, S., Kessel, D., Corbett, T. H., Renis, H. E., Court, B. A. and Zemlicka, J. : Unsaturated and carbocyclic nucleoside analogues: synthesis, antitumor and antiviral activity. J. Med. Chem, 34, 421 (1991)
- O-Yang, C., Wu, H. Y., Fraser-Smith, E. B. and Walker, K. A. M. : Synthesis of 4'-Cyanothymidine and anlogues as potent inhibitors of HIV. Tetrahedron Lett. 33, 37 (1992) https://doi.org/10.1016/S0040-4039(00)77667-2
- Maag, H., Rydzewski, R. M., McRoberts, M. J., Crawford-Ruth, D., Verheyden, J. P. H. and Prisbe, E. J. : Synthesis and anti-HIV activity of 4'-azido- and 4'-methoxynucleosides. J. Med. Chem. 35, 1440 (1992) https://doi.org/10.1021/jm00086a013
- Maag, H., Nelson, J. T., Rios Steiner, J. L. and Prisbe, E. J. : Solid-state and solution conformations of the potent HIV inhibitor, 4'-azidothymidine. J. Med. Chem. 37, 431 (1994) https://doi.org/10.1021/jm00030a001
-
Chen, M. S., Stuttman, R. T., Papp, E., Cannon, P. D., McRoberts, M. J., Bach, C., Copeland, W. C. and Wang, T. S. F. : Selective action of 4'-azidothymidine triphosphate on reverse transcriptase of human immuno-deficiency virus type 1 and human DNA polymerase
$\alpha$ and$\beta$ . Biochemistry 32, 6002 (1993) - Matsuda, A., Takenuki, K., Itoh, H., Sasaki, T. and Ueda, T. : Radical deoxygenation of tert-alcohols in 2'-branched-chain sugar pyrimidine nucleosides: synthesis and antileukemic activity of 2'-deoxy-2'(S)-methylcytidine. Chem. Pharm. Bull. 35, 3967 (1987)
- Matsuda, A., Takenuki, K., Sasaki, T. and Ueda, T. : Radical deoxygenation of tert-alcohols in 1-(2-C-alkylpentofuranosyl) pyrimidines: synthesis of (2'S)-2'-deoxy-2'-C-methylcytidine, an antileukemic nucleoside. J. Med. Chem. 34, 234 (1991)
- Hong, J. H., Shim, M. J., Ro, B. O. and Ko, O. H. : An efficient synthesis of novel carbocyclic nucleosides with use of ring-closing metathesis from D-lactose. J. Org. Chem. 67, 6837 (2002) https://doi.org/10.1021/jo0202536
- Kim, J. and Hong, J. H. : Synthesis of novel apionucleosides: a short and concise synthesis of 2-deoxyapio-L- furanosyl acetate from D-lactose. Carbohydr. Res. 338, 705 (2003)
- Grubbs, R. H. and Chang, S. : Recent advances in olefin metathesis and its application in organic synthesis. Tetrahedron 54, 4413 (1998)
- Ko, O. H. and Hong, J. H. : Efficient synthesis of novel carbocyclic nucleosides via sequential Claisen rearrangement and ring-closing metathesis. Tetrahedron Lett. 43, 6399 (2002) https://doi.org/10.1016/S0040-4039(02)01384-9
-
Hong, J. H., Oh, C. H. and Cho, J. H. : Stereocontrolled synthesis of novel 6'(
$\alpha$ )-hydroxy carbovir analogues. Tetrahedron 59, 6103 (2003) - Gurjar, M. K. and Maheshwar, K. : Stereoselective synthesis of a novel carbocyclic nucleoside. J. Org. Chem. 66, 7552 (2001) https://doi.org/10.1021/jo010718c
- Crimmins, M. T., King, B. w., Zuercher, W. J. and Choy, A. L. : An efficient, general asymmetric synthesis of carbocyclic nucleosides: application of an asymmetric aldol/ring-closing metathesis strategy. J. Org. Chem. 65, 8499 (2000)