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Amidines pyrimidines, 1,4,5,6-tetrahydro

The other main reaction in this class is the Dieckmann-type cyclization of the intermediates (163) from 4(6)-halo-5-ethoxycarbonylpyrimidines with AC-substituted /3-alanine esters and nitriles, and related compounds, to give 5,6,7,8-tetrahydro-5-oxopyrido[2,3-[Pg.221]

Pyrimidin 4-Hydroxy-2-methyl-4-(nonafluor-butyl)-l(3),4,5,6-tetrahydro- E14a/2, 459 (En-on + Amidin)... [Pg.599]

See other pages where Amidines pyrimidines, 1,4,5,6-tetrahydro is mentioned: [Pg.198]    [Pg.169]    [Pg.439]    [Pg.594]    [Pg.542]    [Pg.314]   
See also in sourсe #XX -- [ Pg.18 , Pg.478 ]



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Tetrahydro-pyrimidines

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