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Covalently assembled resorcin[4]arenes and molecular tweezers: a chiral recognition rationale by NMR
Authors:Gloria Uccello Barretta  Federica Balzano  Federica Aiello  Francesca Nardelli  Alessia Ciogli  Andrea Calcaterra
Affiliation:1. Dipartimento di Chimica e Chimica Industriale, Università di Pisa, Pisa, Italygloria.uccello.barretta@unipi.it;3. Dipartimento di Chimica e Chimica Industriale, Università di Pisa, Pisa, Italy;4. Dipartimento di Chimica e Tecnologie del Farmaco, Università di Roma “La Sapienza”, Roma, Italy
Abstract:Chiral diamides and tetramidic resorcin[4]arenes deriving from (R,R)-1,2-diaminocyclohexane and (S,S)-1,2-diphenylethylendiamine, and a valine containing resorcin[4]arene have been compared by NMR in the enantiodiscrimination of mandelic acid. The relevance of cooperation between side arms and external surface of resorcin[4]arene core has been ascertained.
Keywords:NMR spectroscopy  resorcin[4]arenes  chiral auxiliaries  stereochemistry  host–guest systems
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