Skeletal rearrangement for water loss from molecular protonated ions of t??butoxycyclohexane
…, PM Gordon, EE Kingston, JS Shannon…
Index: Diakiw, Vladimir; Gordon, Patrick M.; Kingston, Eric E.; Shannon, James S.; Lacey, Michael J. Organic Mass Spectrometry, 1989 , vol. 24, p. 615 - 619
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Abstract
Abstract Isotopic labelling and chemical substitution support the proposition that the skeletal rearrangement for water loss from molecular protonated ions of t-butoxycyclohexane involves competition between three reaction pathways. The principal reaction pathway (83%) involves migration of the t-butyl group to the 2-(6-) position of the cyclohexyl ring with reciprocal hydrogen transfer. A second reaction pathway (12%) involves ring contraction ...
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