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Absolute configuration of seco-eudesmanolide inuloxin D from experimental and predicted chiroptical studies of its 4-O-acetyl derivative.
Johnson, Jordan L; Santoro, Ernesto; Zatout, Roukia; Petrovic, Ana G; Cimmino, Alessio; Superchi, Stefano; Evidente, Antonio; Berova, Nina D; Polavarapu, Prasad L.
Afiliação
  • Johnson JL; Department of Chemistry, Vanderbilt University, Nashville, Tennessee, USA.
  • Santoro E; Department of Chemistry, Vanderbilt University, Nashville, Tennessee, USA.
  • Zatout R; Department of chemical Sciences, University of Naples Federico II, Naples, Italy.
  • Petrovic AG; Laboratoire de Mycologie, de Biotechnologie et de l'Activité Microbienne (LaMyBAM), Département de Biologie Appliquée, Université des Frères Mentouri, Constantine, Algeria.
  • Cimmino A; Department of Chemical and Biological Sciences, New York Institute of Technology, New York, New York, USA.
  • Superchi S; Department of chemical Sciences, University of Naples Federico II, Naples, Italy.
  • Evidente A; Department of Science, University of Basilicata, Potenza, Italy.
  • Berova ND; Department of chemical Sciences, University of Naples Federico II, Naples, Italy.
  • Polavarapu PL; Department of Chemistry, Columbia University, New York, New York, USA.
Chirality ; 33(5): 233-241, 2021 05.
Article em En | MEDLINE | ID: mdl-33598968
ABSTRACT
Sesquitepenoids inuloxins A-D, belonging to different subgroups, were isolated from Dittrichia viscosa and showed potential biocontrol of some parasitic plants as Pelipanche, Orobanche, and Cuscuta species. The absolute configurations of the first three inuloxins A-C were previously determined by using experimental and computational chiroptical spectroscopic methods. The absolute configuration of inuloxin D remains to be established. The bioactive inuloxin E, closely related to inuloxin D, was recently isolated from the same plant organic extract. The same relative configuration of inuloxin D was assigned to inuloxin E by comparison of their NMR spectroscopic data. The absolute configurations of inuloxin D and inuloxin E are suggested in this work by analysis of the experimental and predicted chiroptical properties of the 4-O-acetyl derivative of inuloxin D.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sesquiterpenos Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Chirality Assunto da revista: BIOLOGIA MOLECULAR / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sesquiterpenos Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Chirality Assunto da revista: BIOLOGIA MOLECULAR / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos