Hetero-Atom Effects on Kinetic Acidities: The Metalation of 1-Methyl-cyclohexene and its 4-Aza- and 4-Oxa-Analogs

Hexane suspensions of trimethylsilylmethylpotassium or butyllithium/potassium tert-butoxide deprotonate 1-methyl-cyclohexene almost exclusively at the methyl group. In contrast 1,4-dimethyl-1,2,3,6-tetrahydropyridine and 4-methyl-5,6-dihydro-2H-pyran preferentially undergo hydrogen/metal-exchange a...

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Bibliographic Details
Main Authors: Etienne Moret, Philippe Schneider, Christian Margot, Manfred Stähle, Manfred Schlosser
Format: Article
Language:deu
Published: Swiss Chemical Society 1985-08-01
Series:CHIMIA
Online Access:https://www.chimia.ch/chimia/article/view/9675
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Summary:Hexane suspensions of trimethylsilylmethylpotassium or butyllithium/potassium tert-butoxide deprotonate 1-methyl-cyclohexene almost exclusively at the methyl group. In contrast 1,4-dimethyl-1,2,3,6-tetrahydropyridine and 4-methyl-5,6-dihydro-2H-pyran preferentially undergo hydrogen/metal-exchange at the nitrogen-distant and, respectively, oxygen-adjacent allylic methylene group. Strong amide bases convert 5,6-dihydro-2H-pyrans into (Z)-pentadienols. The latter ring-opening reaction follows a concerted and not a stepwise pathway (E2 rather than E1cb-irrev, as a novel «common intermediate»-criterion reveals).
ISSN:0009-4293
2673-2424