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<i>Planar-to-Planar</i> Chirality Transfer in the Excited State. Enantiodifferentiating Photoisomerization of Cyclooctenes Sensitized by Planar-Chiral Paracyclophane
54
Citations
23
References
2011
Year
Sensitized Photochirogenic ReactionSynthetic PhotochemistryOrganic ChemistryPlanar-chiral ParacyclophaneChemistryOptogeneticsPhotoredox ProcessCyclooctenes SensitizedPhotophysical PropertyProchiral SubstratesBiophysicsHealth SciencesPlanar-chiral SensitizerPhotochemistryMechanistic PhotochemistryQuantum ChemistryEnantioselective SynthesisBiomolecular EngineeringNatural SciencesExcited State
Photochemical planar-to-planar chirality transfer was effected by using (R)-[10]paracyclophane-12-carboxylates as a planar-chiral sensitizer and (Z)-cyclooctene and (Z,Z)-1,5-cyclooctadiene as prochiral substrates to give a planar-chiral (E)- and (E,Z)-isomer in up to 44% and 87% enantiomeric excess, respectively, the latter of which being the highest ever reported for a sensitized photochirogenic reaction.
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