ACID-CATALYZED PHOTOSUBSTITUTION OF 5-FLUORO-1,3-DIMETHYLURACIL WITH SUBSTITUTED BENZENES

被引：9

作者：

SEKI, K

OHKURA, K

机构：

[1] Faculty of Pharmaceutical Sciences, Higashi-Nippon-Gakuen University, Ishikari-Tobetsu

来源：

NUCLEOSIDES & NUCLEOTIDES | 1992年 / 11卷 / 2-4期

关键词：

D O I：

10.1080/07328319208021723

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

The substantial photosubstitution of 5-fluoro-1,3-dimethyluracil with substituted benzenes is first achieved by the addition of trifluoroacetic acid to the reaction mixture. The presence of protons is essential for the formation of 5-aryl-1,3-dimethyluracils.

引用

页码：521 / 527

页数：7

共 16 条

[1]

BHATIA K, 1975, J PHYS CHEM-US, V77, P1888

[2] URACIL DERIVATIVES - SITES AND KINETICS OF PROTONATION OF THE RADICAL-ANIONS AND THE UV-SPECTRA OF THE C(5) AND C(6) H-ATOM ADDUCTS [J].