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Domino Reactions Involving the Branched C–N and CC Cleavage of Enaminones Toward Pyridines Synthesis

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Domino_Reactions_Involving_the_Branched_C_N_and_C_C_Cleavage_of_Enaminones_Toward_Pyridines_Synthesis/2244055
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The copper-catalyzed cascade reactions of enaminones and ammonium chloride have led to the unprecedented synthesis of 4-unsubstituted pyridines of both symmetrical and unsymmetrical structures. Under the aerobic copper-catalyzed conditions, the branched transformations of enaminones with C–N and CC bond cleavage provide the C2-C3/C5-C6 and C4 building blocks to construct the pyridine ring, respectively. The CC cleavage that provides the C4 atom in the pyridine product is the first example showing the reactivity of an enaminone as the donor of one carbon synthon.
创建时间:
2016-02-16
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