Literature DB >> 19007284

Stereostructure assignment of medium-sized rings through an NMR-computational combined approach. Application to the new germacranes ketopelenolides C and D.

Ernesto Fattorusso1, Paolo Luciano, Adriana Romano, Orazio Taglialatela-Scafati, Giovanni Appendino, Marianna Borriello, Caterina Fattorusso.   

Abstract

The new germacrane derivatives ketopelenolides C and D have been isolated from great mugwort (Artemisia arborescens). Their stereostructure elucidation exemplifies some of the most common pitfalls facing the configurational assignment of medium-sized polyfunctionalized compounds. It was established through a combined strategy including chemical derivatization, NMR data analysis, molecular modeling, and quantum-mechanical calculations including a comparison between experimental 13C NMR data and a Boltzmann-weighted average of DFT-calculated 13C NMR chemical shifts.

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Year:  2008        PMID: 19007284     DOI: 10.1021/np8003547

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  1 in total

1.  The structure elucidation of isomalyngamide K from the marine cyanobacterium Lyngbya majuscula by experimental and DFT computational methods.

Authors:  Bingnan Han; Uwe M Reinscheid; William H Gerwick; Harald Gross
Journal:  J Mol Struct       Date:  2011-03-15       Impact factor: 3.196

  1 in total

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