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- W1963593695 abstract "Cyclisation of substrates 1–4 occurs readily to give the corresponding 2,6-disubstituted tetrahydropyran or piperidine. The geometry about the carbon–carbon double bond of the Michael acceptor within the substrate is shown to have a significant impact on the diastereoselectivity of the cyclisation process." @default.
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- W1963593695 date "1996-01-01" @default.
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- W1963593695 title "Michael addition of N- and O-centred nucleophiles to tethered acrylates. The role of double bond geometry in controlling the diastereoselectivity of cyclisations leading to 2,6-disubstituted tetrahydropyrans and piperidines" @default.
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- W1963593695 doi "https://doi.org/10.1039/p19960000967" @default.
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