| Literature DB >> 21604733 |
Georgia S Lemen1, John P Wolfe.
Abstract
A new method for the stereoselective synthesis of tetrahydropyrroloindoles and hexahydropyrroloquinolines of general structure 8 is described. These products are formed through cascade Pd-catalyzed coupling reactions between aryl chlorides and unsaturated amine substrates 5. A single catalyst effects an intramolecular N-arylation reaction followed by an intermolecular alkene carboamination reaction to generate two rings, three bonds, and one stereocenter with good chemoselectivity, diastereoselectivity, and chemical yield.Entities:
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Year: 2011 PMID: 21604733 PMCID: PMC3118464 DOI: 10.1021/ol201123b
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005