Glucosinolate turnover in Brassicales species to an oxazolidin-2-one, formed via the 2-thione and without formation of thioamide-Reference-Cited by-同舟云学术

Glucosinolate turnover in Brassicales species to an oxazolidin-2-one, formed via the 2-thione and without formation of thioamide

Published:2018-09 Issue: Volume:153 Page:79-93
ISSN:0031-9422
Container-title:Phytochemistry
language:en
Short-container-title:Phytochemistry

Author:

Agerbirk Niels,Matthes Annemarie,Erthmann Pernille Ø.,Ugolini Luisa,Cinti Susanna,Lazaridi Eleni,Nuzillard Jean-Marc,Müller Caroline,Bak Søren,Rollin Patrick,Lazzeri Luca

Funder

Torben og Alice Frimodts Fond

Danish Council for Independent Research, Technology and Production Sciences

Publisher

Elsevier BV

Subject

Horticulture,Plant Science,Molecular Biology,General Medicine,Biochemistry

Reference82 articles.

1. Isoferuloyl derivatives of five seed glucosinolates in the crucifer genus Barbarea;Agerbirk;Phytochemistry,2011

2. Glucosinolate structures in evolution;Agerbirk;Phytochemistry,2012

3. Glucosinolate hydrolysis products in the crucifer Barbarea vulgaris include a thiazolidine-2-one from a specific phenolic isomer as well as oxazolidine-2-thiones;Agerbirk;Phytochemistry,2015

4. A saponin correlated with variable resistance of Barbarea vulgaris to the diamondback moth Plutella xylostella;Agerbirk;J. Chem. Ecol.,2003

5. Host plant dependent metabolism of 4-hydroxybenzylglucosinolate in Pieris rapae: substrate specificity and effects of genetic modification and plant nitrile hydratase;Agerbirk;Insect biochem. Mol. Biol.,2007

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