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Chiral Bis(pyridylimino)isoindoles: A Highly Modular Class of Pincer Ligands for Enantioselective Catalysis
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Citations
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References
2008
Year
Asymmetric CatalysisEnantioselective SynthesisEngineeringChiral WedgesMetal CenterChiral BisOrganic ChemistryBackside AttackOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryHeterocycle ChemistryPincer LigandsHighly Modular ClassBiomolecular Engineering
Protect your back: Chiral wedges (red, see scheme) at the wingtips of bis(2-pyridylimino)isoindole (bpi) pincer ligands with an appropriate protective hedge (green), to block the metal center from backside attack, in the backbone represent a new class of efficient 3d-metal catalysts. These catalysts gave excellent enantioselectivities in the iron-catalyzed hydrosilylation of arylketones and in the cobalt-catalyzed cyclopropanation of alkenes. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2008/z801150_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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