65.7
[1]. Andreas Schmidt, et al. Syntheses, pi-stacking interactions and base-pairings of uracil pyridinium salts and uracilyl betaines with nucleobases. Org Biomol Chem. 6 Aug 1;4(16):356-66.
[]. Stephan Denifl, et al. Electron attachment to chlorouracil: a comparison between 6-ClU and 5-ClU. J Chem Phys. 4 Jan 8;1():74-9.
[3]. Y W Lee, et al. Tumor uptake of radiolabelled pyrimidine bases and pyrimidine nucleosides in animal models--V. 6-[36Cl]chlorouracil, 6-[8Br]bromouracil and 6-[13I]iodouracil. Int J Nucl Med Biol. 1984;11(3-4):6-6.
[4]. Z Kazimierczuk, et al. Photochemical transformation of 6-chlorouracil and some alkylated analogues. Biochim Biophys Acta. 1971 Dec 16;54():157-66.
[5]. Zhibo Yang, et al. Influence of halogenation on the properties of uracil and its noncovalent interactions with alkali metal ions. Threshold collision-induced dissociation and theoretical studies. J Am Chem Soc. 4 Dec 15;16(49):1617-6.
P61-P64-P71-P8-P3+P35-P34+P34-P36+P364-P45-P51
GHS7