1 |
Katsuki, T. and Sharpless, K. B. : The first practical method for asymmetric epoxidation. J. Am. Chem. Soc. 102, 5974 (1980).
DOI
|
2 |
Dale, J. A., Dull, D. L., and Mosher, H. S. : -trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines. J. Org. Chem. 34, 2543 (1969).
DOI
|
3 |
Altona, C. and Sundaralingam, M. : Conformational analysis of the sugar ring in nucleosides and nucleotides. A new description using the concept of pseudorotation. J. Am. Chem. Soc. 94, 8105 (1972).
DOI
|
4 |
Hodgson, D. M., Gibbs, A. R. and Drew, M, G. B. : Mechanism and applications of lithium amide-induced asymmetric rearrangements of 4-substituted and 4,4-disubstituted cyclopentene oxides to cyclopentenols. J. Chem. Soc., Perkin Trans. 1, 24, 3579 (1999).
|
5 |
Kim, J. W., Choi, B. G. and Hong, J. H. : Stereoselective synthesis and antiviral activity of novel 4'(a)-hydroxymethyl and 6'(a)-methyl dually brached carbocyclic nucleosides. Bull. Kor. Chem. Soc. 25, 1812 (2004).
DOI
ScienceOn
|
6 |
Kauppinen, S., Vester, B. and Wengel, J. : Locked nucleic acid (LNA): High affinity targeting of RNA for diagnostics and therapeutics. Drug Discovery Today 10, 287 (2005).
|
7 |
Costanzi, S., Joshi, B. V., Maddileti, S., Mamedova, L., Gonzalez-Moa, M. J., Marquez, V. E., Harden, T. K. and Jacobson, K. A. : Human receptor: molecular modeling leads to the rational design of a novel agonist based on a unique conformational preference. J. Med. Chem. 48, 8108 (2005).
DOI
ScienceOn
|
8 |
Besada, P., Shin, D. H., Costanzi, S., Ko, H., Mathe, C., Gagneron, J., Gosselin, G., Maddileti, S., Harden, T. K. and Jacobson, K. A. : Structure-activity relationships of uridine 5''- diphosphate analogues at the human receptor. J. Med. Chem. 49, 5532 (2006).
DOI
ScienceOn
|
9 |
Ohno, M., Costanzi, S., Kim, H. S., Kempeneers, V., Vastmans, K., Herdewijn, P., Maddileti, S., Gao, A.-G., Harden, T. K. and Jacobson, K. A. : Nucleotide analogues containing 2- oxa-bicyclo[2.2.1]heptane and l-alpha-threofuranosyl ring systems: interactions with P2Y receptors. Bioorg. Med. Chem. 12, 5619 (2004).
DOI
ScienceOn
|
10 |
Obika, S., Uneda, T., Sugimoto, T., Nanbu, D., Minami, T., Doi, T. and Imanishi, T. : 2'-O,4'-C-Methylene bridged nucleic acid (2',4'-BNA): synthesis and triplex-forming properties. Bioorg. Med. Chem. 9, 1001 (2001).
DOI
ScienceOn
|
11 |
Kim, H. S. and Jacobson, K. A. : Synthesis of a novel conformationally locked carbcyclic nucleoside ring system. Org. Lett. 5, 1665 (2003).
DOI
ScienceOn
|
12 |
Kim, S. A., Lee, H. M., Ryu, J.-S. and Kim, H. S. : Synthesis of conformationally locked methanocarba-uridine as a precursor for nucleotides agonizing receptor. Synlett 7, 1055 (2007).
|
13 |
Jin, Y. L. and Hong, J. H. : Synthesis and antiviral activity of novel 4'-branched carbcyclic c-nucleoside. Bull. Kor. Chem. Soc. 26, 1366 (2005).
과학기술학회마을
DOI
ScienceOn
|
14 |
Obika, S., Morio, K.-I., Nanbu, D., Hari, Y., Itoh, H. and Imanishi, T. : Synthesis and conformation of 3',4'-BNA monomers, 3'-O,4'-C Methyleneribonucleosides. Tetrahedron 58, 3039 (2002).
DOI
ScienceOn
|
15 |
Balmer, E., Germain, A., Jackson, W. P., and Lygo, B. : Larger scale preparation of optically-active allylic alcohols. J. Chem. Soc., Perkin Trans. 1: Org. Bio-Org. Chem. 4, 399 (1993).
|