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Enol triflates pyrimidines

The reaction of 4-bromobenzaldehyde with substituted acetophenones and urea gave aryl-substituted pyrimidin-2-ones 63 or hexahydro-l//,8//-pyrimido[4,5-rfJpyrimidin-2,7-diones 64, depending on the nature of the acetophenone substituent and the solvent <04CHE194>. Two new approaches to 2,4-dialkylamino-substituted 6,7-dihydro-5//-benzocyclohepta[l,2-c( pyrimidines were developed, one based on the reaction of substituted cyanamides and the enol triflate of 1-benzosuberone, and the other based on nucleophilic displacements at C2 and C4 of... [Pg.316]

Pyrimidines from enol triflates and two nitrile molecules... [Pg.431]

Trimethylsilylpyrimidinium triflate, derived from pyrimidine and trimethylsilyl triflate, adds silylated enol ethers to form 1,4-dihydropyrimidines. /V-Acylpyrimidinium tetrafluoroborates undergo analogous reactions (85H(23)207). [Pg.213]


See other pages where Enol triflates pyrimidines is mentioned: [Pg.115]    [Pg.513]    [Pg.513]    [Pg.61]    [Pg.382]    [Pg.153]   
See also in sourсe #XX -- [ Pg.44 ]




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