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Rh(III)-Catalyzed Diastereoselective Annulation of Amides with Quinone Monoacetals: Access to Bridged Nine-Membered Heterocycles via C–H Activation
53
Citations
67
References
2017
Year
Chemical EngineeringCross-coupling ReactionEngineeringHeterocyclicNovel OrganocatalystsUnprecedented RhBridged Nine-membered HeterocyclesC-h Bond FunctionalizationPlausible MechanismOrganic ChemistryOrganometallic CatalysisCatalysisSynthetic ChemistryChemistryHeterocycle ChemistryQuinone MonoacetalsC–h Activation
An unprecedented Rh(III)-catalyzed annulation of various benzamides and acrylamides with quinone monoacetals was developed for the facile and efficient one-pot synthesis of bridged nine-membered benzo[c]azonine-1,5(2H)-diones and 2-azabicyclo[4.3.1]dec-4-ene-3,8-diones. It is the first example of synthesis of nine-membered heterocycles through Rh(III)-catalyzed C-H bond functionalization, and both aryl and vinyl C-H bonds are tolerant in this reaction. A plausible mechanism is proposed on the basis of control experiments.
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