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Synthetic approaches and functionalizations of imidazo1,2-apyrimidines: an overview of the decade

机译:咪唑并1,2-a嘧啶的合成方法和功能化:十年概述

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Imidazo1,2-apyrimidine has been receiving significant attention in the synthetic chemistry community through different chemosynthetic methodologies viz., multicomponent reactions, condensation reactions, intramolecular cyclizations, tandem reaction, carbon-hydrogen, carbon-carbon, carbon-nitrogen bond formation, aza-Michael-Mannich reaction, chiral compounds synthesis etc. The mechanisms for the selected reactions are also discussed to observe the formation of this heterocyclic moiety. This review comprehensively summarizes the recently reported various synthetic approaches along with its functionalization at 3-positions to construct this privileged scaffold for further use in the development of new chemosynthetic strategies and drug development due to its wide range of applications in medicinal chemistry.
机译:咪唑并[1,2-a]嘧啶通过不同的化学合成方法,即多组分反应、缩合反应、分子内环化、串联反应、碳-氢、碳-碳、碳-氮键形成、氮-迈克尔-曼尼希反应、手性化合物合成等,在合成化学界受到广泛关注。还讨论了所选反应的机理,以观察该杂环部分的形成。本文综述了近年来报道的各种合成方法及其在3位的功能化,构建了这种特殊的支架,由于其在药物化学中的广泛应用,可进一步用于开发新的化学合成策略和药物开发。

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