AAAAAA

   
Results: 1-11 |
Results: 11
A new method for the synthesis of N-2-alkylguanosines using Mitsunobu reaction as a key step
Authors: Kozai, S Yorikane, A Maruyama, T
Citation: S. Kozai et al., A new method for the synthesis of N-2-alkylguanosines using Mitsunobu reaction as a key step, NUCLEOS NUC, 20(8), 2001, pp. 1523-1531
Synthesis of N-2-alkylguanosine using Mitsunobu reaction as a key step
Authors: Maruyama, T Yorikane, A Kozai, S
Citation: T. Maruyama et al., Synthesis of N-2-alkylguanosine using Mitsunobu reaction as a key step, NUCLEOS NUC, 20(4-7), 2001, pp. 935-936
Synthesis and hypnotic activities of 4-thio analogues of N-3-substituted uridines
Authors: Kozai, S Maruyama, T Kimura, T Yamamoto, I
Citation: S. Kozai et al., Synthesis and hypnotic activities of 4-thio analogues of N-3-substituted uridines, CHEM PHARM, 49(9), 2001, pp. 1185-1188
Method for the synthesis of uric acid derivatives
Authors: Maruyama, T Kozai, S Sasaki, F
Citation: T. Maruyama et al., Method for the synthesis of uric acid derivatives, NUCLEOS NUC, 19(7), 2000, pp. 1193-1203
Reaction of 7-(2-mesyloxy-2-phenylethyl)theophylline with amines: Synthesis of 1,2,3,6-tetrahydro-6-imino-2-oxo-7H-purine derivatives
Authors: Kozai, S Ogimoto, K Maruyama, T
Citation: S. Kozai et al., Reaction of 7-(2-mesyloxy-2-phenylethyl)theophylline with amines: Synthesis of 1,2,3,6-tetrahydro-6-imino-2-oxo-7H-purine derivatives, TETRAHEDRON, 56(39), 2000, pp. 7685-7690
Participation of acidic sites on catalyst in hydrodenitrogenation of quinoline
Authors: Kozai, S Kabashima, H Hattori, H
Citation: S. Kozai et al., Participation of acidic sites on catalyst in hydrodenitrogenation of quinoline, FUEL, 79(3-4), 2000, pp. 305-310
Synthesis of N-aryl uracils and hypoxanthines and their biological properties
Authors: Maruyama, T Kozai, S Uchida, M
Citation: T. Maruyama et al., Synthesis of N-aryl uracils and hypoxanthines and their biological properties, NUCLEOS NUC, 18(4-5), 1999, pp. 661-671
Synthesis of 8-substituted analogues of 2 '-deoxy-2 '-fluoroadenosine
Authors: Maruyama, T Kozai, S Manabe, T Yazima, Y Satoh, Y Takaku, H
Citation: T. Maruyama et al., Synthesis of 8-substituted analogues of 2 '-deoxy-2 '-fluoroadenosine, NUCLEOS NUC, 18(11-12), 1999, pp. 2433-2442
Introduction of a benzoyl group onto riboside in aqueous solution: One-step syn thesis of 6-chloropurine 2 ',3 '-di-O-benzoylriboside
Authors: Kozai, S Takamatsu, S Izawa, K Maruyama, T
Citation: S. Kozai et al., Introduction of a benzoyl group onto riboside in aqueous solution: One-step syn thesis of 6-chloropurine 2 ',3 '-di-O-benzoylriboside, TETRAHEDR L, 40(23), 1999, pp. 4355-4358
Synthesis of 9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine bearing aselectively removable protecting group
Authors: Maruyama, T Takamatsu, S Kozai, S Satoh, Y Izawa, K
Citation: T. Maruyama et al., Synthesis of 9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine bearing aselectively removable protecting group, CHEM PHARM, 47(7), 1999, pp. 966-970
Synthesis and biological activity of 9-(2,6-difluorobenzyl)-9H-purines bearing chlorine
Authors: Kozai, S Maruyama, T
Citation: S. Kozai et T. Maruyama, Synthesis and biological activity of 9-(2,6-difluorobenzyl)-9H-purines bearing chlorine, CHEM PHARM, 47(4), 1999, pp. 574-575
Risultati: 1-11 |