作者:Toshio Itahara、Reiko Ebihara、Yukiko Fujii、Miki Tada
DOI:10.1246/cl.1986.1319
日期:1986.8.5
Reaction of thymines with Na2S2O8 in water resulted in selective oxidation of the methyl group at 5-position of thymines. Oxidation of thymines with Na2S2O8 in hydrochloric acid gave 5-chloro-6-hydroxy-5,6-dihydrothymines and in acetic acid containing NaCl gave 6-acetoxy-5-chloro-5,6-dihydrothymines which were converted to 6-alkoxy-5-chloro-5,6-dihydrothymines with alcohols. The reaction of uracils also gave similar products together with 5-chlorouracils.
胸腺
嘧啶与Na2S2O8在
水中的反应导致了胸腺
嘧啶5位甲基基团的选择性氧化。在
盐酸中用Na2S2O8氧化胸腺
嘧啶生成5-
氯-6-羟基-5,6-二氢胸腺
嘧啶,而在含NaCl的
醋酸中则生成6-乙氧基-5-
氯-5,6-二氢胸腺
嘧啶,这些化合物可以与醇转化为6-烷氧基-5-
氯-5,6-二氢胸腺
嘧啶。尿
嘧啶的反应也产生了类似的产物,同时伴随着5-
氯尿
嘧啶的生成。