Coinage (Au, Ag, Cu) metal-catalyzed (3 + 2) annulation of α-aminoketones and electron-deficient alkynes as a route to 3-EWG-substituted pyrroles†

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
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Abstract

Coinage (Au, Ag, Cu) metal-catalyzed (3 + 2) annulation of α-aminoketones and electron-deficient alkynes provides a modular one-step route to a variety of 3-EWG-substituted pyrroles. Apart from gold(i) complexes, which “open any door” and catalyze the annulation regardless of the identity of the alkyne EWGs [–SO2R, –CO2R, –PO(OR)2], the other cheaper coinage metal (first of all Cu, but also Ag) species function as alternative catalysts for the selective activation of alkynylsulfones and their conversion to 3-sulfonylpyrroles. The developed catalytic annulation operates under relatively mild conditions (5 mol% of a coinage metal catalyst, DCE, 80 °C) and provides a high functional group tolerance (36 examples; yields up to 99%). The synthetic utility of the obtained products was illustrated by practical post-modification of either the pyrrole backbone, or the peripheral substituents.

Abstract Image

金、银、铜)金属催化的α-氨基酮和缺电子炔的(3 + 2)环化反应,作为制备 3-EWG 取代的吡咯的途径†。
硬币(金、银、铜)金属催化的 α-aminoketones 和缺电子炔的 (3 + 2) 环化反应提供了一条模块化的一步法路线,可以得到各种 3-EWG 取代的吡咯。金(I)配合物可以 "打开任何一扇门 "并催化环化反应,而与炔烃 EWG [-SO2R、-CO2R、-PO(OR)2] 的特性无关。除了金(I)配合物之外,其他廉价的硬币金属(首先是铜,也包括银)也可作为替代催化剂,选择性地活化炔砜并将其转化为 3-磺酰基吡咯。所开发的催化环化反应在相对温和的条件下进行(5 摩尔% 的共价金属催化剂、DCE、80 °C),并具有较高的官能团耐受性(36 个实例;收率高达 99%)。通过对吡咯骨架或外围取代基进行实用的后修饰,说明了所获产物的合成用途。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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