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Title: Domino Heck-aza-Michael reactions: efficient access to 1-substituted tetrahydro-beta-carbolines. Author: Priebbenow DL, Henderson LC, Pfeffer FM, Stewart SG. Journal: J Org Chem; 2010 Mar 05; 75(5):1787-90. PubMed ID: 20131765. Abstract: A simple and efficient palladium-catalyzed domino reaction for the synthesis of a series of C1-substituted tetrahydro-beta-carbolines is described. This domino process involves a Heck reaction at the indole 2-position of a halogenated tryptamine precursor, followed by intramolecular aza-Michael addition.[Abstract] [Full Text] [Related] [New Search]