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• W2951567342 endingPage "114" @default.
• W2951567342 startingPage "57" @default.
• W2951567342 abstract "Publisher Summary This chapter discusses the chemistry, biological activity, and the uses of 1,2,3-triazolopyrimidines. There are three possible classes of 1,2,3-triazolopyrimidines according to the site of fusion of the two rings: [1,5-a]-fused, [1,5-c]-fused, and [4,5-d]-fused compounds that are included because of their chemotherapeutic potential. Pyrimidines have attracted the attention of organic chemists and biochemists because of their role in biological systems, particularly in nucleic acids, which contain pyrimidines and purines as the main nucleobases. The aza analogs of purines––mainly the triazolo and tetrazolo [x,y-z] pyrimidines—are also important. The aza analogs of purines and the annulation of a pyrimidine ring to an existing ring are also reviewed in the chapter. The order of the site of fusion onto the pyrimidine ring is denoted by the letter “z.” The letters “x” and “y” indicate the site of fusion onto the triazole ring. The arrangement of the subdivisions is dependent on the extent of already published work." @default.
• W2951567342 created "2019-06-27" @default.
• W2951567342 creator A5051335127 @default.
• W2951567342 creator A5078795493 @default.
• W2951567342 date "1998-01-01" @default.
• W2951567342 modified "2023-09-22" @default.
• W2951567342 title "1,2,3-Triazolo[x, y-z]pyrimidines" @default.
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• W2951567342 doi "https://doi.org/10.1016/s0065-2725(08)60831-4" @default.
• W2951567342 hasPublicationYear "1998" @default.

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