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- W2055274083 abstract "A new stereocenter is formed by ring-rearrangement metathesis (RRM), which has now been extended to diastereoselective processes. Selectivities are catalyst- and substrate-dependent. In these conversions yielding carbo- and heterocycles, d.r. values of up to 14:1 were obtained. For example, cyclooctadiene 1 was converted into piperideine 2 at room temperature and with high diastereoselectivity (Ts=toluene-4-sulfonyl)." @default.
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- W2055274083 date "2006-02-06" @default.
- W2055274083 modified "2023-10-18" @default.
- W2055274083 title "Diastereoselective Ring-Rearrangement Metathesis" @default.
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- W2055274083 doi "https://doi.org/10.1002/anie.200503321" @default.
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