Publication | Closed Access
Synthesis and Application of Chiral Spiro Phospholane Ligand in Pd-Catalyzed Asymmetric Allylation of Aldehydes with Allylic Alcohols
149
Citations
13
References
2005
Year
Asymmetric CatalysisCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented SynthesisAllylic AlcoholsOrganic ChemistryOrganometallic CatalysisCatalysisHigh YieldChemistryPd-catalyzed Asymmetric AllylationHomoallylic AlcoholsPharmacologyStereoselective SynthesisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
[reaction: see text] A novel chiral monodentate spiro phenylphospholane ligand 4 was prepared from a readily accessible, enantiomerically pure 1,1'-spirobiindane-7,7'-diol in high yield. This ligand has proven to be efficient for Pd-catalyzed enantioselective allylation of aldehydes with allylic alcohols. Aromatic, heteroaromatic, and aliphatic aldehydes gave homoallylic alcohols in good enantioselectivities (up to 83% ee) and excellent anti diastereoselectivities (up to 99:1 dr).
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