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吡咯的功能化及其转化潜力的最新进展。

Recent Advances in Functionalization of Pyrroles and their Translational Potential.

机构信息

Department of Pharmaceutial Technology (Process Chemistry), National Institute of Pharmaceutical Education & Research (NIPER) S.A.S. Nagar, Mohali, 160062, India.

Center of Innovative and Applied Bioprocessing (CIAB), Department of Biotechnology (DBT), Government of India, Sector 81 (Knowledge City), S.A.S., Nagar, 140306, Punjab, India.

出版信息

Chem Rec. 2021 Apr;21(4):715-780. doi: 10.1002/tcr.202100010. Epub 2021 Mar 2.

Abstract

Among the known aromatic nitrogen heterocycles, pyrrole represents a privileged aromatic heterocycle ranging its occurrence in the key component of "pigments of life" to biologically active natural products to active pharmaceuticals. Pyrrole being an electron-rich heteroaromatic compound, its predominant functionalization is legendary to aromatic electrophilic substitution reactions. Although a few excellent reviews on the functionalization of pyrroles including the reports by Baltazzi in 1963, Casiraghi and Rassu in 1995, and Banwell in 2006 are available, they are fragmentary and over fifteen years old, and do not cover the modern aspects of catalysis. A review covering a comprehensive package of direct functionalization on pyrroles via catalytic and non-catalytic methods including their translational potential is described. Subsequent to statutory yet concise introduction, the classical functionalization on pyrroles using Lewis acids largely following an ionic mechanism is discussed. The subsequent discussion follows the various metal-catalyzed C-H functionalization on pyrroles, which are otherwise difficult to implement by Lewis acids. A major emphasize is given on the radical based pyrrole functionalization under metal-free oxidative conditions, which is otherwise poorly highlighted in the literature. Towards the end, the current development of pyrrole functionalization under photocatalyzed and electrochemical conditions is appended. Only a selected examples of substrates and important mechanisms are discussed for different methods highlighting their scopes and limitations. The aromatic nucleophillic substitution on pyrroles (being an electron-rich heterocycle) happened to be the subject of recent investigations, which has also been covered accentuating their underlying conceptual development. Despite great achievements over the past several years in these areas, many challenges and problems are yet to be solved, which are all discussed in summary and outlook.

摘要

在已知的芳香族含氮杂环化合物中,吡咯是一种重要的芳香杂环,它存在于“生命色素”的关键组成部分、生物活性天然产物和活性药物中。吡咯是一种富电子杂芳环化合物,其主要官能团化反应是著名的芳香亲电取代反应。虽然有一些关于吡咯官能团化的优秀综述,包括 Baltazzi 在 1963 年、Casiraghi 和 Rassu 在 1995 年以及 Banwell 在 2006 年的报告,但它们是不完整的,而且已经有十五年的历史了,并没有涵盖催化的现代方面。本文综述了通过催化和非催化方法对吡咯进行直接官能团化的综合方法,包括其转化潜力。在进行法定但简洁的介绍后,讨论了使用路易斯酸对吡咯进行经典官能团化的方法,这些方法主要遵循离子机制。随后的讨论遵循了各种金属催化的 C-H 官能团化在吡咯上的应用,这些方法用路易斯酸是难以实现的。重点介绍了在无金属氧化条件下基于自由基的吡咯官能团化,这在文献中很少被强调。最后,还附录了在光催化和电化学条件下吡咯官能团化的最新发展。对于不同的方法,只讨论了一些底物和重要的机制的例子,强调了它们的范围和局限性。吡咯的芳香亲核取代(作为一种富电子杂环)恰好是最近研究的主题,这也在强调其潜在概念发展的背景下进行了讨论。尽管在过去几年中在这些领域取得了巨大的成就,但仍有许多挑战和问题有待解决,这些都在总结和展望中进行了讨论。

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