دورية أكاديمية

Dihydroazolopyrimidines: Past, Present and Perspectives in Synthesis, Green Chemistry and Drug Discovery.

التفاصيل البيبلوغرافية
العنوان: Dihydroazolopyrimidines: Past, Present and Perspectives in Synthesis, Green Chemistry and Drug Discovery.
المؤلفون: Desenko, Serhiy M., Gorobets, Mykola Yu., Lipson, Victoria V., Sakhno, Yana I., Chebanov, Valentyn A.
المصدر: Chemical Record; Feb2024, Vol. 24 Issue 2, p1-50, 50p
مصطلحات موضوعية: DRUG discovery, PHARMACEUTICAL chemistry, CHEMICAL properties, DRUG design, PURINES, SUSTAINABLE chemistry
مستخلص: Dihydroazolopyrimidines are an important class of heterocycles that are isosteric to natural purines and are therefore of great interest primarily as drug‐like molecules. In contrast to the heteroaromatic analogs, synthetic approaches to these compounds were developed much later, and their chemical properties and biological activity have not been studied in detail until recently. In the review, different ways to build dihydroazolopyrimidine systems from different building blocks are described – via the initial formation of a partially hydrogenated pyrimidine ring or an azole ring, as well as a one‐pot assembly of azole and azine fragments. Special attention is given to modern approaches: multicomponent reactions, green chemistry, and the use of non‐classical activation methods. Information on the chemical properties of dihydroazolopyrimidines and the prospects for their use in the design of drugs of various profiles are also summarized in this review. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:15278999
DOI:10.1002/tcr.202300244