Literature DB >> 16441090

An unusual oxalylated tetramic acid from the New Zealand basidiomycete Chamonixia pachydermis.

Gerhard Lang1, Anthony L J Cole, John W Blunt, Murray H G Munro.   

Abstract

An unusual oxalylated tetramic acid, pachydermin (1), has been isolated from the New Zealand basidiomycete Chamonixiapachydermis. The full structure, which was not directly accessible by NMR methods, was deduced from that of a degradation product, 5-(3-chloro-4-hydroxybenzylidene)tetramic acid (2). The degradation product 2 exhibited mild antibacterial activity against Bacillus subtilis.

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Year:  2006        PMID: 16441090     DOI: 10.1021/np050488n

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


  3 in total

1.  An efficient synthesis of tetramic acid derivatives with extended conjugation from L-ascorbic acid.

Authors:  Biswajit K Singh; Surendra S Bisht; Rama P Tripathi
Journal:  Beilstein J Org Chem       Date:  2006-12-06       Impact factor: 2.883

2.  Ruthenium-catalyzed selective hydrogenation of bis-arylidene tetramic acids. Application to the synthesis of novel structurally diverse pyrrolidine-2,4-diones.

Authors:  Christos S Karaiskos; Dimitris Matiadis; John Markopoulos; Olga Igglessi-Markopoulou
Journal:  Molecules       Date:  2011-07-20       Impact factor: 4.411

3.  Mediation of metal chelation in cysteine-derived tetramate systems.

Authors:  Ruirui Zhang; Miroslav Genov; Alexander Pretsch; Dagmar Pretsch; Mark G Moloney
Journal:  Chem Sci       Date:  2021-12-02       Impact factor: 9.825

  3 in total

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