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Synthesis of Racemic and Enantiomerically Pure (<i>R*,R*,R*</i>)‐Tris(α‐methylbenzyl)phosphane − X‐ray Crystal Structures of the Phosphane Oxides and Borane Complexes
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Citations
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References
2003
Year
EngineeringOrganic ChemistryEnantiomerically PureChemistry‐Symmetric Phosphane 1Phosphane OxidesBorane ComplexesInorganic CompoundOrganometallic CatalysisInorganic ChemistryDiversity-oriented SynthesisAsymmetric SynthesisAsymmetric CatalysisCrystallographyInorganic SynthesisBiomolecular EngineeringNatural SciencesCoordination ComplexMolecular ComplexC 3Synthetic Chemistry
Abstract An asymmetric synthesis of C 3 ‐symmetric phosphane 1 has been achieved. Two of the α‐methylbenzyl groups were introduced as nucleophiles (using an α‐methylbenzyl Grignard reagent), and asymmetry was introduced by resolution using ( R )‐α‐methylbenzylamine. The final α‐methylbenzyl group was introduced as an electrophile (α‐methylbenzyl iodide) in a modestly selective reaction. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
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