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首页> 外文期刊>Angewandte Chemie >Cobalt-Catalyzed Annulation of Salicylaldehydes and Alkynes to Form Chromones and 4-Chromanones
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Cobalt-Catalyzed Annulation of Salicylaldehydes and Alkynes to Form Chromones and 4-Chromanones

机译:钴催化的水杨醛和炔烃环化形成色酮和4-色酮

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摘要

A unique cobalt(I)-diphosphine catalytic system has been identified for the coupling of salicylaldehyde (SA) and an internal alkyne affording a dehydrogenative annulation product (chromone) or a reductive annulation product (4-chromanone) depending on the alkyne substituents. Distinct from related rhodium(I)-and rhodium(III)-catalyzed reactions of SA and alkynes, these annulation reactions feature aldehyde C-H oxidative addition of SA and subsequent hydrometalation of the C=O bond of another SA molecule as common key steps. The reductive annulation to 4-chromanones also involves the action of Zn as a stoichiometric reductant. In addition to these mechanistic features, the Co-I catalysis described herein is complementary to the Rh-I- and Rh-III-catalyzed reactions of SA and internal alkynes, particularly in the context of chromone synthesis.
机译:已经确定了独特的钴(I)-二膦催化体系,用于水杨醛(SA)和内部炔烃的偶联,取决于炔烃取代基,该炔烃可提供脱氢环化产物(色酮)或还原性环化产物(4-苯并二氢吡喃酮)。与相关的SA和炔烃的铑(I)和铑(III)催化反应不同,这些环化反应的特征是SA的醛C-H氧化加成反应以及随后另一个SA分子的C = O键的加氢金属化是常见的关键步骤。还原成4-发色环的环化还涉及锌作为化学计量还原剂的作用。除了这些机制特征外,本文所述的Co-I催化是SA和内部炔烃的Rh-I-和Rh-III催化的反应的补充,特别是在色酮合成的情况下。

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