Literature DB >> 23844767

Agarsenone, a Cadinane Sesquiterpenoid from Commiphora erythraea.

Stefano Santoro1, Stefano Superchi, Federica Messina, Ernesto Santoro, Ornelio Rosati, Claudio Santi, M Carla Marcotullio.   

Abstract

Agarsenone (1), a new cadinane sesquiterpenoid, was isolated from the resin of Commiphora erythraea. The structures of 1 and its decomposition products agarsenolides (2a and 2b) and myrrhone (3) were established by extensive NMR spectroscopic analysis. The absolute configuration of 3 and the relative and absolute configurations of 1 were assigned by comparison of experimental and calculated optical rotatory dispersion and electronic circular dichroism spectra.

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Year:  2013        PMID： 23844767     DOI： 10.1021/np400114b

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


  2 in total

1.  Assignment Through Chiroptical Methods of The Absolute Configuration of Fungal Dihydropyranpyran-4-5-Diones Phytotoxins, Potential Herbicides for Buffelgrass (Cenchrus ciliaris) Biocontrol.

Authors:  Ernesto Santoro; Giuseppe Mazzeo; Giulia Marsico; Marco Masi; Giovanna Longhi; Stefano Superchi; Antonio Evidente; Sergio Abbate
Journal:  Molecules       Date:  2019-08-21       Impact factor: 4.411

2.  Absolute Configuration Assignment to Chiral Natural Products by Biphenyl Chiroptical Probes: The Case of the Phytotoxins Colletochlorin A and Agropyrenol.

Authors:  Ernesto Santoro; Stefania Vergura; Patrizia Scafato; Sandra Belviso; Marco Masi; Antonio Evidente; Stefano Superchi
Journal:  J Nat Prod       Date:  2020-02-24       Impact factor: 4.050
  2 in total

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