Substitution and Ring Opening of Fused Pyrimidines Using Their Activation by Azido And Triazolyl Groups
27th Croatian Meeting of Chemists and Chemical Engineers: Book of Abstracts 2021
Māris Turks, Irina Novosjolova, Ērika Bizdēna

We have developed synthesis of 2,6-bis-triazolyl-purine derivatives 4 (Y = 1,2,3-triazole) and demonstrated their application in SNAr reactions by substituting C(6) position of purine with a broad range of N-, S-, Se-, C-, O-, and P-nucleophiles (Scheme 1).[1] 2,6-Bis-triazolyl-purine derivatives 4 and their SNAr products 5 are fluorescent and this has led to development of ion sensing, cell imaging systems and applications in materials science.[2] On the other hand, azidosubstituted fused pyrimidines of type 2 exhibit azide-tetrazole tautomerism, which was instrumental to develop novel substitution methodologies (nucleophile-nucleofuge dance) around the cycle[3] and also pyrimidine ring opening reactions leading to compounds of type 3


Atslēgas vārdi
purines, azidopurines, triazolylpurines, fused pyrimidines
Hipersaite
https://27hskiki.hkd.hr/book-of-abstracts/

Turks, M., Novosjolova, I., Bizdēna, Ē. Substitution and Ring Opening of Fused Pyrimidines Using Their Activation by Azido And Triazolyl Groupsa. No: 27th Croatian Meeting of Chemists and Chemical Engineers: Book of Abstracts, Horvātija, Veli Lošinj, 5.-8. oktobris, 2021. Zagreb: Croatian Chemical Society, 2021, 18.-18.lpp. e-ISSN 2757-0754.

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