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Direct Hiyama Cross-Coupling of Enaminones With Triethoxy(aryl)silanes and Dimethylphenylsilanol

https://doi.org/10.1021/ol202202a

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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The Direct Approach

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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ChemInform Abstract: Direct Hiyama Cross‐Coupling of Enaminones with Triethoxy(aryl)silanes and Dimethylphenylsilanol.

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Homoleptic chelating N-heterocyclic carbene complexes of palladium immobilized within the pores of SBA-15/IL (NHC–Pd@SBA-15/IL) as heterogeneous catalyst for Hiyama reaction

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inferred← citeshttps://doi.org/10.1039/c7ob00619eopenalex-snapshot

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inferred← citeshttps://doi.org/10.1039/c7sc00156hopenalex-snapshot

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inferred← citeshttps://doi.org/10.1039/c8nj06412aopenalex-snapshot

Metal-free, green and efficient oxidative α halogenation of enaminones by halo acid and DMSO

inferred← citeshttps://doi.org/10.1039/d1ob00595bopenalex-snapshot

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