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Pyrimidines Af-oxidation

The synthetic uses of pyrimidines in the construction of non-heterocycles appear to be relatively small. While the ring opening reaction of a pyrimidine Af-oxide with phenylmag-nesium bromide has been reported to give benzaldehyde upon hydrolysis (it thus plays the same role as DMF) (67JOC3788) the Diels-Alder capabilities of the pyrimidines do, on the other hand, appear to hold considerable promise in organic chemistry. [Pg.484]

Pyridine and pyrimidine Af-oxides 1320-1230 7.58-8.13 m-s m N-0 str, hydrogen bonding lowers... [Pg.196]


See other pages where Pyrimidines Af-oxidation is mentioned: [Pg.330]    [Pg.105]   
See also in sourсe #XX -- [ Pg.43 , Pg.153 ]




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