52602-65-0Relevant articles and documents
PREPARATION OF ALKYL- AND PHENYL-SUBSTITUTED PYRIMIDINES
Martinez, A. Garcia,Fernandez, A. Herrera,Alvarez, R. Martinez,Vilar, E. Teso,Fraile, A. Garcia,et. al.
, p. 1929 - 1932 (1987)
Vinyltrifluoromethanesulfonates (triflates) 1, which are obtained from the corresponding ketones, react in an excess of pure nitriles (acetonitrile, propionitrile, benzonitrile) at 80 deg C (20 h) to form substituted pyrimidines 5 and 8 in good yields
A New and Convenient Synthesis of Alkyl and Aryl Pyrimidines
Martinez, A. Garcia,Herrera, A.,Martinez, R.,Teso, E.,Garcia, A.,et al.
, p. 1237 - 1241 (2007/10/02)
Vinyl triflates 1, which are obtained easily from the corresponding ketones, react in an excess of pure nitrile (80 deg C/20 hours) to form tri- and tetra-substituted alkyl and arylpyrimidines 4 and 5 in good yields (45-87percent).An isomeric mixture of p
SYNTHESIS OF PYRIMIDINES FROM VINYL CHLORIDES AND NITRILES BY THE RITTER REACTION
Borodaev, S. V.,Zubkova, O. V.,Luk'yanov, S. M.
, p. 2100 - 2103 (2007/10/02)
Chloroalkenes with a chlorine atom at the vinylic position and also phenylacetylene react with nitriles in the presence of trifluoromethanesulfonic acid to form tri- and tetrasubstituted pyrimidines.