Highly diastereoselective synthesis of orthoquinone monoketals through λ13-iodane-mediated oxidative dearomatization of phenols - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Angewandte Chemie International Edition Année : 2008

Highly diastereoselective synthesis of orthoquinone monoketals through λ13-iodane-mediated oxidative dearomatization of phenols

Résumé

(Chemical Equation Presented) Versatile chiral substrates for asymmetric synthesis are formed through the spiroketalization of phenols with a chiral substituted ethanol unit O-tethered to the ortho position upon treatment with PhI-(OAc)2 (see example; TFE = 2,2,2-tri-fluoroethanol). Intermediates with a six-membered iodine(III)-containing ring (the natural localized molecular orbitals associated with the I-C6 bond are shown) undergo ligand coupling to give the spiroketals. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.

Dates et versions

hal-01613258 , version 1 (09-10-2017)

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L. Pouységu, Stefan Chassaing, D. Dejugnac, A.-M. Lamidey, Karinne Miqueu, et al.. Highly diastereoselective synthesis of orthoquinone monoketals through λ13-iodane-mediated oxidative dearomatization of phenols. Angewandte Chemie International Edition, 2008, 47 (19), pp.3552-3555. ⟨10.1002/anie.200705816⟩. ⟨hal-01613258⟩
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