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- W2940231570 abstract "A palladium catalyzed cascade process involving syn-chloropalladation, intramolecular olefin insertion, and oxidative C-Cl bond formation reactions was demonstrated for the synthesis of dichlorinated tetrahydroquinolines in high yields (up to 93%). The N-propargyl arylamines having a tethered α,β-unsaturated carbonyl moiety underwent a regioselective syn-chloropalladation followed by a Heck-type reaction to deliver the tetrahydroquinoline scaffold. The rare insertion of the second chlorine atom was rationalized comprising a PdII/IV catalytic cycle and oxidative cleavage of the C-PdII bond." @default.
- W2940231570 created "2019-04-25" @default.
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- W2940231570 date "2019-04-19" @default.
- W2940231570 modified "2023-09-24" @default.
- W2940231570 title "Palladium-Catalyzed Regioselective <i>Syn</i>-Chloropalladation–Olefin Insertion–Oxidative Chlorination Cascade: Synthesis of Dichlorinated Tetrahydroquinolines" @default.
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- W2940231570 doi "https://doi.org/10.1021/acs.orglett.9b01295" @default.
- W2940231570 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31001984" @default.
- W2940231570 hasPublicationYear "2019" @default.
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