Literature DB >> 23514637

Structure and absolute configuration of methyl (3R)-malonyl-(13S)-hydroxycheilanth-17-en-19-oate, a sesterterpene derivative from the roots of Aletris farinosa.

Victoria L Challinor1, Sonet Chap, Reginald P Lehmann, Paul V Bernhardt, James J De Voss.   

Abstract

We report the isolation and structure elucidation of a new cheilanthane sesterterpene from the roots of Aletris farinosa that possesses an unusual malonate half-ester functional group. The structure of 1 was determined via mass spectrometry and 1D and 2D NMR spectroscopy, while its absolute configuration was determined via X-ray crystallographic analysis performed on its methyl ester derivative 2.

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Year:  2013        PMID: 23514637     DOI: 10.1021/np400035n

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


  2 in total

1.  Neutral Loss Ion Mapping Experiment Combined with Precursor Mass List and Dynamic Exclusion for Screening Unstable Malonyl Glucoside Conjugates.

Authors:  Min Yang; Zhe Zhou; Shuai Yao; Shangrong Li; Wenzhi Yang; Baohong Jiang; Xuan Liu; Wanying Wu; Hua Qv; De-an Guo
Journal:  J Am Soc Mass Spectrom       Date:  2015-09-03       Impact factor: 3.109

2.  Biosynthetic insights provided by unusual sesterterpenes from the medicinal herb Aletris farinosa.

Authors:  Victoria L Challinor; Ryne C Johnston; Paul V Bernhardt; Reginald P Lehmann; Elizabeth H Krenske; James J De Voss
Journal:  Chem Sci       Date:  2015-07-06       Impact factor: 9.825

  2 in total

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