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Cobalt-Catalyzed Intramolecular Alkyne/Benzocyclobutenone Coupling: C–C Bond Cleavage via a Tetrahedral Dicobalt Intermediate

机译:钴催化的分子内炔烃/苯并环丁烯酮偶联:通过四面体二钴中间体进行C–C键裂解

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摘要

A Co(0)-catalyzed intramolecular alkyne/benzocyclobutenone coupling through C–C cleavage of benzocyclobutenones is described. Co2(CO)8/P[3, 5-(CF3)2C6H3]3 was discovered to be an effective metal/ligand combination, which exhibits complementary catalytic activity to the previously established rhodium catalyst. In particular, the C8-substituted substrates failed in the Rh system, but succeeded with the Co catalysis. Experimental and computational studies show that the initially formed tetrahedral dicobalt-alkyne complex undergoes C1–C2 activation via oxidative addition with Co(0), followed by migratory insertion and reductive elimination to give the β-naphthol products.
机译:描述了通过苯并环丁烯酮的CC裂解的Co(0)催化的分子内炔烃/苯并环丁烯酮偶联。发现Co 2(CO)8 / P [3,5-(CF 3)2 C 6 H 3] 3是有效的金属/配体组合,其表现出与先前建立的铑催化剂互补的催化活性。特别是,C8取代的底物在Rh系统中失效,但在Co催化下成功。实验和计算研究表明,最初形成的四面体二钴-炔烃复合物通过与Co(0)的氧化加成反应经历C1-C2活化,然后通过迁移插入和还原消除得到β-萘酚产物。

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