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1.3.5- Triazine derivatives, pyrimidine base analogs

All these findings, as well as the similarity of UV spectra - caused dioxotetrahydrotriazine to be classified as the simplest member of the formerly known 6-substituted derivatives. These derivatives are not interesting in connection with the analogs of natural pyrimidine bases and have been reviewed elsewhere. The structure of allantoxaidine and its appurtenance to the triazine series have been recently demonstrated by its unequivocal synthesis. [Pg.194]

The chemistry of the 6-aza analogs of pyrimidine bases which has been developed from the biochemical aspect since about 1956 was based on work reported in relatively numerous older papers. In spite of the fact that 6-azauracil was prepared only in 1947 and suitable syntheses were described only quite recently, substances of this type and methods of their preparation had been known for a long time. The chemistry of 6-aza analogs of pyrimidine bases is therefore relatively closely linked with the chemistry of the 1,2,4-triazine derivatives. [Pg.204]

Two types of addition to pyrimidine bases appear to exist. The first, the formation of pyrimidine photohydrates, has been the subject of a detailed review.251 Results suggest that two reactive species may be involved in the photohydration of 1,3-dimethyluracil.252 A recent example of this type of addition is to be found in 6-azacytosine (308) which forms a photohydration product (309) analogous to that found in cytosine.253 The second type of addition proceeds via radical intermediates and is illustrated by the addition of propan-2-ol to the trimethylcytosine 310 to give the alcohol 311 and the dihydro derivative 312.254 The same adduct is formed by a di-tert-butyl peroxide-initiated free radical reaction. Numerous other photoreactions involving the formation by hydrogen abstraction of hydroxyalkyl radicals and their subsequent addition to heterocycles have been reported. Systems studied include 3-aminopyrido[4,3-c]us-triazine,255 02,2 -anhydrouri-dine,256 and sym-triazolo[4,3-fe]pyridazine.257 The photoaddition of alcohols to purines is also a well-documented transformation. The stereospecific addition of methanol to the purine 313, for example, is an important step in the synthesis of coformycin.258 These reactions are frequently more... [Pg.290]


See other pages where 1.3.5- Triazine derivatives, pyrimidine base analogs is mentioned: [Pg.191]    [Pg.192]    [Pg.102]    [Pg.232]    [Pg.102]    [Pg.344]   
See also in sourсe #XX -- [ Pg.203 ]




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1,2,4-Triazine derivatives, pyrimidine base

Base analogs

Pyrimidin derivatives

Pyrimidine analogs

Pyrimidine bases

Pyrimidine bases derivation

Pyrimidines 1.3.5- triazine

Pyrimidines derivatives

Triazin derivative

Triazine derivatives

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