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- W2011956018 abstract "Für die Addition des Phenoxycarbens bzw. Phenoxycarbenoids an Olefine wurden Konkurrenzkonstanten ermittelt (Isobuten 1, Ketendiäthylacetal 16, Trimethyläthylen 1.05, Tetramethyläthylen 0.43, Cyclohexen 0.2). Die Umsetzung von Fluormethyl-, Chlormethyl- und Brommethyl-phenyläther (2, 1, 3) mit salzfreiem Butyllithium in Cyclohexen liefert exo/endo-7-Phenoxy-norcaran (12) im Verhältnis 6.0, 4.2 und 2.1. Mit LiBr-haltiger Base ist das Epimerenverhältnis von der Abgangsgruppe nahezu ganz unabhängig." @default.
- W2011956018 created "2016-06-24" @default.
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- W2011956018 date "1967-12-18" @default.
- W2011956018 modified "2023-10-09" @default.
- W2011956018 title "Untersuchungen über Heterocarbene, IX. Zur Selektivität des Phenoxycarbens bzw. Phenoxycarbenoids" @default.
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- W2011956018 doi "https://doi.org/10.1002/jlac.19677090111" @default.
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