Publication | Closed Access
A New Atropisomeric Molecular Structure for Efficient Enantiodifferentiation
37
Citations
9
References
1993
Year
Soluble Inclusion ComplexEnantioselective SynthesisEngineeringAsymmetric SynthesisOrganic ChemistryStereoselective SynthesisChemistryNovel Atropisomer 1Natural Product SynthesisAsymmetric CatalysisEfficient EnantiodifferentiationBiophysicsBiomolecular Engineering
Enantioselective clathrate formation and sorption is possible with the enantiomers of the novel atropisomer 1. Racemic 1 is easily accessible from 2,2′-dibromophenyl and fluorenone; the (S)-(+) enantiomer can be obtained pure with (−)-fenchone on formation of the sparingly soluble inclusion complex. Other potential applications are envisaged for these atropisomers in analysis and in asymmetric synthesis.
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