Oxidative Dearomatization of Phenols and Anilines via λ3- and λ5-Iodane-Mediated Phenylation and Oxygenation
- Authors
- Publication Date
- Jan 31, 2005
- Identifiers
- DOI: 10.3390/10010201
- OAI: oai:mdpi.com:/1420-3049/10/1/201/
- Source
- MDPI
- Keywords
- Language
- English
- License
- Green
- External links
Abstract
Treatment of 2-methylphenols with chloro(diphenyl)-λ3-iodane led to theirregioselective dearomatizing 2-phenylation into cyclohexa-2,4-dienone derivatives via aproposed ligand coupling reaction. In the same vein of investigation, treatment of2-methylanilines with the λ5-iodane 2-iodoxybenzoic acid IBX reagent led to theirregioselective dearomatization into previously undescribed ortho-quinol imines.