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- W4247873470 abstract "Bei Raumtemperatur gelingt mit EtAlCl2 die diastereoselektive [1,3]-Umlagerung von 2,5-Dihydrooxepinen (siehe Schema). Eine modulare Synthese von Dihydrooxepinen ermöglicht den Einbau von Substituenten an jeder beliebigen Ringposition, sodass mit dieser Lewis-Säure-vermittelten [1,3]-Ringverengung eine Vielzahl polysubstituierter Cyclopentene zugänglich ist." @default.
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- W4247873470 date "2005-05-17" @default.
- W4247873470 modified "2023-10-18" @default.
- W4247873470 title "Stereoselective Lewis Acid Mediated [1,3] Ring Contraction of 2,5-Dihydrooxepins as a Route to Polysubstituted Cyclopentenes" @default.
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- W4247873470 doi "https://doi.org/10.1002/ange.200500088" @default.
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