Multiple hydroxyphenethyl glucosinolate isomers and their tandem mass spectrometric distinction in a geographically structured polymorphism in the crucifer Barbarea vulgaris-Reference-Cited by-同舟云学术

Multiple hydroxyphenethyl glucosinolate isomers and their tandem mass spectrometric distinction in a geographically structured polymorphism in the crucifer Barbarea vulgaris

Published:2015-07 Issue: Volume:115 Page:130-142
ISSN:0031-9422
Container-title:Phytochemistry
language:en
Short-container-title:Phytochemistry

Author:

Agerbirk Niels^ORCID,Olsen Carl Erik,Heimes Christine,Christensen Stina,Bak Søren,Hauser Thure P.

Funder

Faculty of Life Sciences, University of Copenhagen

Danish Council for Independent Research, Technology and Production Sciences

Publisher

Elsevier BV

Subject

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

Reference56 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. Seasonal variation in leaf glucosinolates and insect resistance in two types of Barbarea vulgaris ssp. arcuata;Agerbirk;Phytochemistry,2001

5. Glucosinolates, flea beetle resistance, and leaf pubescence as taxonomic markers in the genus Barbarea (Brassicaceae);Agerbirk;Phytochemistry,2003

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