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现代方法合成与转化实用价值的苯并噻唑衍生物。

Modern Approaches to the Synthesis and Transformations of Practically Valuable Benzothiazole Derivatives.

机构信息

E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Street, 664033 Irkutsk, Russia.

出版信息

Molecules. 2021 Apr 10;26(8):2190. doi: 10.3390/molecules26082190.

Abstract

The review is devoted to modern trends in the chemistry of 2-amino and 2-mercapto substituted benzothiazoles covering the literature since 2015. The reviewed heterocycles belong to biologically active and industrially demanded compounds. Newly developed synthesis methods can be divided into conventional multistep processes and one-pot, atom economy procedures, realized using green chemistry principles and simple reagents. The easy functionalization of the 2-NH and 2-SH groups and the benzene ring of the benzothiazole moiety allows considering them as highly reactive building blocks for organic and organoelement synthesis, including the synthesis of pharmacologically active heterocycles. The review provides a summary of findings, which may be useful for developing new drugs and materials and new synthetic approaches and patterns of reactivity.

摘要

这篇综述致力于讨论 2-氨基和 2-巯基取代苯并噻唑的化学,涵盖了 2015 年以来的文献。所综述的杂环化合物属于具有生物活性和工业需求的化合物。新开发的合成方法可分为常规多步过程和一锅法、原子经济性方法,这些方法利用绿色化学原理和简单试剂实现。苯并噻唑部分的 2-NH 和 2-SH 基团以及苯环易于官能化,可将其视为有机和有机元素合成(包括药理学活性杂环的合成)的高反应性构建模块。综述提供了研究结果的总结,这可能对开发新药和材料以及新的合成方法和反应模式有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0b3/8070523/7292734fbc85/molecules-26-02190-sch001.jpg

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