铑(II)催化的 N-磺酰基-1,2,3-三唑的脱氮转化

IF 2.5 3区 化学 Q2 CHEMISTRY, ORGANIC
Mohammad Mahdavi, Fatemeh Doraghi, Mohammad Hossein Morshedsolouk, Samaneh Ghofrani, Bagher Larijani
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引用次数: 0

摘要

N-磺酰基-1,2,3-三唑是在金属催化剂,特别是铑(II)络合物存在下生成α-亚氨基碳烯中间体的重要前体。由于亲电碳氮和亲核氮的存在,这些活性中间体可以很容易地加入到许多环化、环加成、C-H 或 O/N/S-H 键插入和官能化反应中。通过这种直接且原子经济的碳烯策略,可以构建大量具有重要药用价值的氮基构筑基块。在本综述中,我们介绍了基于α-亚氨基铑(II)碳烯中间体的 N-磺酰基-1,2,3-三唑的转化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rhodium(II)-Catalyzed Denitrogenative Transformations of N-Sulfonyl-1,2,3-triazoles
N-Sulfonyl-1,2,3-triazoles are valuable precursors for the generation of α-imino carbene intermediates in the presence of the metal catalysts, especially rhodium(II) complexes. Due to the presence of electrophilic carbene and nucleophilic nitrogen, these reactive intermediates can easily be incorporated into many annulations, cycloadditions, C-H or O/N/S-H bond insertions and functionalization reactions. A large number of pharmaceutically important nitrogen-based building blocks can be constructed via this direct and atom-economical carbene strategy. In this review, we have described the transformations of N-sulfonyl-1,2,3-triazoles based on α-imino rhodium(II) carbene intermediates.
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来源期刊
CiteScore
5.40
自引率
3.60%
发文量
752
审稿时长
1 months
期刊介绍: The European Journal of Organic Chemistry (2019 ISI Impact Factor 2.889) publishes Full Papers, Communications, and Minireviews from the entire spectrum of synthetic organic, bioorganic and physical-organic chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. The following journals have been merged to form two leading journals, the European Journal of Organic Chemistry and the European Journal of Inorganic Chemistry: Liebigs Annalen Bulletin des Sociétés Chimiques Belges Bulletin de la Société Chimique de France Gazzetta Chimica Italiana Recueil des Travaux Chimiques des Pays-Bas Anales de Química Chimika Chronika Revista Portuguesa de Química ACH—Models in Chemistry Polish Journal of Chemistry.
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