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- 8. The synthesis of trypanocides. Part I. Some pyrimidylaminoquinoline derivatives. P. A. Barrett, F. H. S. Curd, W. Hepworth
, J. Chem. Soc.
, 1953
, 50
- 688. Electronic levels in pyrimidines: the crystal spectrum of 2-amino-4-chloro-6-methylpyrimidine. L. E. Lyons, J. C. Mackie
, J. Chem. Soc.
, 1963
, 3665
- 9. The synthesis of trypanocides. Part II. 4-Amino-6-(2-amino-1 : 6-dimethylpyrimidinium-4-amino)-1 : 2-dimethylquinolinium (“Antrycide”) salts and related compounds. A. D. Ainley, F. H. S. Curd, W. Hepworth, A. G. Murray, C. H. Vasey
, J. Chem. Soc.
, 1953
, 59
- Synthesis and biological evaluation of 5-substituted O
4-alkylpyrimidines as CDK2 inhibitors. Francesco Marchetti, Céline Cano, Nicola J. Curtin, Bernard T. Golding, Roger J. Griffin, Karen Haggerty, David R. Newell, Rachel J. Parsons, Sara L. Payne, Lan Z. Wang, Ian R. Hardcastle
, Org. Biomol. Chem.
, 2010
, 8
, 2397
- A prototype solid phase synthesis of pteridines and related heterocyclic compounds. Colin L. Gibson, Salvatore La Rosa, Colin J. Suckling
, Org. Biomol. Chem.
, 2003
, 1
, 1909
- Synthesis, antimicrobial evaluation and molecular modeling of some novel phenothiazine derivatives. Ahmed A. Fadda, Ahmed Fekri, Nesma M. Bayoumy
, RSC Adv.
, 2015
, 5
, 80844
- A multi-fused heat-resistant energetic compound constructed by hydrogen bonds. Yong Hu, Wen-Shuai Dong, Zu-Jia Lu, Han Zhang, Jian-Guo Zhang
, Chem. Commun.
, 2023
, 59
, 9864
- 9. Synthetic antimalarials. Part XI. The effect of variation of substituents in derivatives of mono- and di-alkylprimidines. R. Hull, B. J. Lovell, H. T. Openshaw, A. R. Todd
, J. Chem. Soc.
, 1947
, 41
- 612. Pyrimidine reactions. Part IV. The methylation of 2,4- and 4,5-diaminopyrimidine and related compounds. D. J. Brown, N. W. Jacobsen
, J. Chem. Soc.
, 1962
, 3172
- Hydrogen bond donor–acceptor–donor organocatalysis for conjugate addition of benzylidene barbiturates via complementary DAD–ADA hydrogen bonding. Franco King-Chi Leung, Jian-Fang Cui, Tsz-Wai Hui, Zhong-Yuan Zhou, Man-Kin Wong
, RSC Adv.
, 2014
, 4
, 26748