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.

Absolute configuration of seco-eudesmanolide inuloxin D from experimental and predicted chiroptical studies of its 4-O-acetyl derivative / Johnson, J. L.; Santoro, E.; Zatout, R.; Petrovic, A. G.; Cimmino, A.; Superchi, S.; Evidente, A.; Berova, N. D.; Polavarapu, P. L.. - In: CHIRALITY. - ISSN 0899-0042. - 33:5(2021), pp. 233-241. [10.1002/chir.23301]

Absolute configuration of seco-eudesmanolide inuloxin D from experimental and predicted chiroptical studies of its 4-O-acetyl derivative

Zatout R.;Cimmino A.
Investigation
;
Superchi S.;Evidente A.
Supervision
;
2021

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.
2021
Absolute configuration of seco-eudesmanolide inuloxin D from experimental and predicted chiroptical studies of its 4-O-acetyl derivative / Johnson, J. L.; Santoro, E.; Zatout, R.; Petrovic, A. G.; Cimmino, A.; Superchi, S.; Evidente, A.; Berova, N. D.; Polavarapu, P. L.. - In: CHIRALITY. - ISSN 0899-0042. - 33:5(2021), pp. 233-241. [10.1002/chir.23301]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/857650
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