Shu Wu, Miaomiao Li, Jiajun Lu, Chi Yang, Yue Huang, Aijun Lin
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Enantioselective Synthesis of Hydrindanes via Palladium-Catalyzed Asymmetric Desymmetrization of Cyclohexadiene Derivatives
We herein disclose a strategy for the asymmetric desymmetrization of cyclohexadiene derivatives via a palladium-catalyzed Heck and tandem Heck/Tsuji-Trost allylic alkoxylation reaction. By employing DCE as the solvent, we obtained a variety of chiral hydrindanes containing an all-carbon quaternary carbon center and a tertiary carbon chiral center in good yields with excellent enantioselectivities. With alcohols as the solvent, the valuable chiral hydrindanes with one quaternary stereocenter and two tertiary centers were constructed with a high level of enantioinduction.
期刊介绍:
Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.