Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds

Literature Information

Publication Date 2019-05-08
DOI 10.1039/C9QO00353C
Impact Factor 5.281
Authors

Zhen Zhang, Xiao-Ming Zhang, Fu-Min Zhang, Shao-Hua Wang


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Abstract

Herein, a novel copper-catalyzed highly diastereoselective cross-dehydrogenative coupling reaction is reported. A broad range of 1,3-dicarbonyl compounds and 8-hydroxyisochromanes are applicable to this methodology, affording tricyclic chromane products in moderate to high yields with continuous stereocenters identical to natural penicitrinols.

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Back cover

Cover

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Back matter

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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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