首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Facile syntehsis of pyrazoles and pyrroles via thermolysis of tetrazolo[1,5-b]pyridazines, tetrazolo[1,5-a]pyrimidines and tetrazolo[1,5-a]pyridines
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Facile syntehsis of pyrazoles and pyrroles via thermolysis of tetrazolo[1,5-b]pyridazines, tetrazolo[1,5-a]pyrimidines and tetrazolo[1,5-a]pyridines

机译:通过四唑并[1,5-b]哒嗪,四唑并[1,5-a]嘧啶和四唑并[1,5-a]吡啶的热解反应可轻松合成吡唑和吡咯

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摘要

A simple and high yielding preparation of pyrazoles and pyrroles is described. Thermolysis of tetrazolo[1,5-b]pyridazines, tetrazolo[1,5-a]pyrimidines and tetrazolo[1,5-a]pyridines allowed easy ring contraction thus providing a facile preparation of cyanopyrazole and cyanopyrrole heterocycles. Since the cyano group is a versatile precursor of other functionalities, the reaction appears of particular interest for the construction of a variety of pyrazoles and pyrroles. The simle preparation of the starting tetrazole derivatives, the relatively mild conditions employed, and the very short reaction times make this versatile procedure of great synthetic utility and applicable both to small and large scale preparation.
机译:描述了吡唑和吡咯的简单且高产率的制备。四唑并[1,5-b]哒嗪,四唑并[1,5-a]嘧啶和四唑并[1,5-a]吡啶的热解使环易于收缩,从而提供了氰基吡唑和氰基吡咯杂环的简便制备方法。由于氰基是其他官能团的通用前体,因此该反应对于构建各种吡唑和吡咯特别感兴趣。起始四唑衍生物的简单制备,所采用的相对温和的条件以及非常短的反应时间,使得这种通用的方法具有很高的合成实用性,并且适用于小规模和大规模的制备。

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