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Ullmann-Goldberg and Buchwald-Hartwig C−N Cross Couplings: Synthetic Methods to Pharmaceutically Potential N-Heterocycles Publisher



Seifinoferest B1 ; Tanbakouchian A2 ; Larijani B1 ; Mahdavi M1
Authors
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Authors Affiliations
  1. 1. Endocrinology and Metabolism Research Centre, Tehran University of Medical Sciences, University of Tehran, Nejatollahi St, Enghelab St, Iran
  2. 2. Department of Chemistry, College of Chemistry, University of Tehran, 16 Azar St, Enghelab St, Iran

Source: Asian Journal of Organic Chemistry Published:2021


Abstract

The Carbon-Nitrogen bond formation has always been an important and useful tool in drug discovery. Its wide applications in synthesizing N-heterocycles, known as the most prevalent moiety in the active pharmacophores, have attracted increasing attention from researchers. In recent years many works were devoted to finding new and more rapid and effective chemo- and regio-selective methods for the synthesis of N-containing heterocycles. Buchwald-Hartwig and Ullman-Goldberg are two proven efficient methods for synthesizing five, six, and seven-membered heterocycles found abundantly in literature. Here, we study these two amination methods more precisely, based on the reaction conditions and the products. © 2021 Wiley-VCH GmbH