Synthesis of [2-14C]-labelled 2,2′-anhydrouridine and 2'-deoxyuridine derivatives. A convenient route to [2-14C]-labelled 5-ethynyl- and 5-ethyl-2′-deoxyuridine
Tài liệu tham khảo
Wataya, 1979, J. Med. Chem., 22, 339, 10.1021/jm00190a001
Chang, 1979, J. Med. Chem., 22, 1137, 10.1021/jm00195a028
Barr, 1983, Biochemistry, 22, 1696, 10.1021/bi00276a027
Shugar, 1973, 295
Bigar, 1979, Adv. Ophthalmol., 38, 105
Heidelberger, 1975, Ann. N.Y. Acad. Sci., 255, 317, 10.1111/j.1749-6632.1975.tb29239.x
Kaul, 1980, J. Pharm. Sci., 69, 531, 10.1002/jps.2600690514
Torrence, 1977, J. Med. Chem., 20, 974, 10.1021/jm00217a026
Cheng, 1976, Antimicrob. Agents Chemother., 10, 119, 10.1128/AAC.10.1.119
Torrence, 1978, J. Med. Chem., 21, 228, 10.1021/jm00200a018
De Clercq, 1979, 275
Jones, 1981, J. Med. Chem., 24, 759, 10.1021/jm00138a024
Szabolcs, 1978, J. Labeled Compd. Radiopharm., 14, 713, 10.1002/jlcr.2580140509
Fel'dman, 1966, Mechenye Biol. Veschestva, Sb. Statei., 2, 5
1967, Chem. Abstr., 66, 55695y
Sekiguchi, 1959, J. Biochem., 46, 1505, 10.1093/oxfordjournals.jbchem.a126947
1960, Chem. Abstr., 54, 13225f
Filip, 1967, J. Labeled Compd., 3, 128, 10.1002/jlcr.2590030208
Filip, 1978, J. Labeled Compd. Radiopharm., 14, 297, 10.1002/jlcr.2580140220
Friedkin, 1956, J. Biol. Chem., 220, 653, 10.1016/S0021-9258(18)65290-1
Kara, 1963, Collect. Czech. Chem. Commun., 28, 1441, 10.1135/cccc19631441
Filip, 1969, J. Labeled Compd., 5, 241, 10.1002/jlcr.2590050305
Ruth, 1982, J. Labeled Compd. Radiopharm., 19, 861, 10.1002/jlcr.2580190706
Robins, 1981, J. Am. Chem. Soc., 103, 932, 10.1021/ja00394a033
Lessor, 1981, J. Org. Chem., 46, 4300, 10.1021/jo00334a043
Zbarsky, 1949, Can. J. Res., 27B, 81, 10.1139/cjr49b-011
Murray, 1958, 588
Sanchez, 1970, J. Mol. Biol., 47, 531, 10.1016/0022-2836(70)90320-7
Marumoto, 1974, Chem. Pharm. Bull. Tokyo, 22, 128, 10.1248/cpb.22.128
Dawson, 1979, J. Labeled Compd. Radiopharm., 16, 335, 10.1002/jlcr.2580160213
Robins, 1982, Can. J. Chem., 60, 554, 10.1139/v82-082
Robins, 1981, Tetrahedron Lett., 22, 421, 10.1016/0040-4039(81)80115-3
Robins, 1983, J. Org. Chem., 48, 1854, 10.1021/jo00159a012
Koyama, 1982, Nucl. Acids Res. Symp. Ser. II, 11, 41
Abrams, 1979, J. Labeled Compd. Radiopharm., 16, 12
Codington, 1964, J. Org. Chem., 29, 558, 10.1021/jo01026a009
Robins, 1976, J. Am. Chem. Soc., 98, 7381, 10.1021/ja00439a046
Cech, 1976, Collect. Czech. Chem. Commun., 41, 3335, 10.1135/cccc19763335
Friedland, 1961, Biochim. Biophys. Acta, 51, 148, 10.1016/0006-3002(61)91025-3
Chang, 1963, J. Med. Chem., 6, 428, 10.1021/jm00340a019
Pichat, 1969, C.R. Acad. Sci. Paris Ser. C., 268, 197
Pichat, 1971, Bull. Soc. Chim. Fr., 2102
Pichat, 1973, Bull. Soc. Chim. Fr., 2715
Huang, 1977, J. Org. Chem., 42, 3821, 10.1021/jo00444a006
Baker, 1966, J. Med. Chem., 9, 66, 10.1021/jm00319a018
Hsi, 1972, J. Labeled Compd., 8, 407, 10.1002/jlcr.2590080306
Burmeister, 1964, Inorg. Chem., 3, 1587, 10.1021/ic50021a025
Fox, 1965, Tetrahedron Lett., 643
Hampton, 1966, Biochemistry, 5, 2076, 10.1021/bi00870a040