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- W4313487824 abstract "A strategy for the palladium-catalyzed intermolecular synthesis of polysubstituted cyclopentenones is reported. The three-component reaction utilizes vinyl iodides and internal alkynes to form the carbon framework of the cyclopentenone with Cr(CO)6 serving as an easy to handle, solid CO surrogate, and a hydrosilane as a hydride source. We demonstrate the scope of the reaction which includes a wide range of functional groups. The reaction is regioselective, with the use of linear or branched vinyl iodides resulting in the α- or β-substituted cyclopentenones, respectively. Further, we show that a two-step sequence from commercially available alkynes can be used to generate cyclopentenone products via formation of the vinyl iodide and subsequent Pauson–Khand-type reaction." @default.
- W4313487824 created "2023-01-06" @default.
- W4313487824 creator A5013291539 @default.
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- W4313487824 creator A5078851035 @default.
- W4313487824 date "2023-01-04" @default.
- W4313487824 modified "2023-09-27" @default.
- W4313487824 title "Intermolecular Pauson–Khand-Type Reaction of Vinyl Iodides with Alkynes and a CO Surrogate" @default.
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- W4313487824 doi "https://doi.org/10.1021/acs.joc.2c02465" @default.
- W4313487824 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36598125" @default.
- W4313487824 hasPublicationYear "2023" @default.
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