Stereospecific and Unspecific Pathways for Aromatization of 1,4-Cyclohexadienes

The aromatization of trans-3,6-dideuterio-1,4-cyclohexadiene (1-d2) to benzene (2) with chromic acid is slightly stereospecific with a diastereomeric excess of 25%. This result is ascribed to two competing mechanisms, a stereospecific 2-electron oxidation with CrVI, and a non-specific 1-electron ox...

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Bibliographic Details
Main Authors: Paul Müller, Nicole Pautex, Hans Hagemann
Format: Article
Language:deu
Published: Swiss Chemical Society 1988-12-01
Series:CHIMIA
Online Access:https://www.chimia.ch/chimia/article/view/9880
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