Literature DB >> 16467943

Unprecedented chemical structure and biomimetic synthesis of erucalexin, a phytoalexin from the wild crucifer Erucastrum gallicum.

M Soledade C Pedras1, Mojmir Suchy, Pearson W K Ahiahonu.   

Abstract

The isolation, structure determination, total synthesis and antifungal activity of erucalexin, a novel phytoalexin produced by the wild crucifer dog mustard are described. Erucalexin is a structurally unique plant alkaloid, representing the first example of a spiro[2H-indole-2,5'(4'H)-thiazol]-3-one, likely derived from a C-3-C-2 carbon migration in a 3-substituted indolyl nucleus.

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Year:  2006        PMID: 16467943     DOI: 10.1039/b515331j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Intramolecular 1,3-dipolar cycloaddition reactions in the synthesis of complex annelated quinolines, α-carbolines and coumarins.

Authors:  Swarup Majumder; Pallabi Borah; Pulak J Bhuyan
Journal:  Mol Divers       Date:  2012-02-29       Impact factor: 2.943

Review 2.  Spirocyclic Motifs in Natural Products.

Authors:  Evgeny Chupakhin; Olga Babich; Alexander Prosekov; Lyudmila Asyakina; Mikhail Krasavin
Journal:  Molecules       Date:  2019-11-17       Impact factor: 4.411

3.  Two cytochromes P450 catalyze S-heterocyclizations in cabbage phytoalexin biosynthesis.

Authors:  Andrew P Klein; Elizabeth S Sattely
Journal:  Nat Chem Biol       Date:  2015-09-21       Impact factor: 15.040

  3 in total

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