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Hydroalkylation of Olefins To Form Quaternary Carbons.

Journal of the American Chemical Society (2019-04-30)
Samantha A Green, Tucker R Huffman, Ruairí O McCourt, Vincent van der Puyl, Ryan A Shenvi
RÉSUMÉ

Metal-hydride hydrogen atom transfer (MHAT) functionalizes alkenes with predictable branched (Markovnikov) selectivity. The breadth of these transformations has been confined to π-radical traps; no sp3 electrophiles have been reported. Here we describe a Mn/Ni dual catalytic system that hydroalkylates unactivated olefins with unactivated alkyl halides, yielding aliphatic quaternary carbons.

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Sigma-Aldrich
trans-(+)-limonene oxide
Sigma-Aldrich
trans-(-)-limonene oxide, ≥95%