Publication | Closed Access
New chiral ammonium salt hosts derived from amino acids: very efficient optical resolution of 2,2′-dihydroxy-1,1′-binaphthyl by complexation with these host compounds
32
Citations
5
References
1997
Year
EngineeringAmino AcidsCo 2Efficient Optical ResolutionHost CompoundsOrganic ChemistryOh GroupsStereoselective SynthesisChemistryHalogenationAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Chiral ammonium salt hosts are prepared from amino acids by transformation of their NH 2 and CO 2 H groups into Me 3 N + Br - and CH 2 OH groups, respectively, via three simple reaction steps; by complexation with these hosts, 2,2′-dihydroxy-1,1′-binaphthyl is resolved very efficiently.
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