Journal of the American Chemical Society · 2003 · 190 citations · 12 references
Natural SciencesChemistryCatalysisOrganometallic ChemistryStructure-activity RelationshipsCatalytic MaterialsCatalytic MechanismsAldehydesAsymmetric CatalysisAsymmetric Catalyst DesignCalcitriol SynthesisEnantioselective CatalysisEnantioselective SynthesisEnantioselectivityNatural Product Synthesis
This work describes the development of a new tridentate ligand effective for the asymmetric catalysis of Nozaki-Hiyama allylation and methallylation. Various aldehydes were allylated or methallylated with good enantioselectivity (86-96%), and a key intermediate of calcitriol lactone synthesis was also obtained with excellent diastereoselectivity (97% de, 91%). The enantioselective reaction catalyzed by this Cr-ligand complex is applicable to a broad range of aldehydes and has great potential for natural product synthesis. Another remarkable feature of this ligand is the stability of the Cr-ligand complex which was recovered after the enantioselective reaction and recycled twice without diminishing the enantioselectivity and yield.
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Marco Bandini, Pier Giorgio Cozzi, Achille Umani‐Ronchi · Angewandte Chemie International Edition · 2000 · 93 citations · Full text