Synthesis of stable isotope-labeled nasturlexins and potential precursors to probe biosynthetic pathways of cruciferous phytoalexins

Divergent reactivity of an indole glucosinolate yields Lossen or Neber rearrangement products: the phytoalexin rapalexin A or a unique β-d-glucopyranose fused heterocycle

(2016) M. S. C. Pedras et al.   CHEMICAL COMMUNICATIONS

The synthesis of sulforaphane analogues and their protection effect against cisplatin induced cytotoxicity in kidney cells

(2015) Taejung Kim et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Multiple binding modes of isothiocyanates that inhibit macrophage migration inhibitory factor

(2015) Emma S. Spencer et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

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

(2015) Niels Agerbirk et al.   PHYTOCHEMISTRY

Expanding the nasturlexin family: Nasturlexins C and D and their sulfoxides are phytoalexins of the crucifers Barbarea vulgaris and B. verna

(2015) M. Soledade C. Pedras et al.   PHYTOCHEMISTRY

Non-indolyl cruciferous phytoalexins: Nasturlexins and tridentatols, a striking convergent evolution of defenses in terrestrial plants and marine animals?

(2015) M. Soledade C. Pedras et al.   PHYTOCHEMISTRY

Dissecting metabolic puzzles through isotope feeding: a novel amino acid in the biosynthetic pathway of the cruciferous phytoalexins rapalexin A and isocyalexin A

(2012) M. Soledade C. Pedras et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

The phytoalexins from cultivated and wild crucifers: Chemistry and biology

(2011) M. Soledade C. Pedras et al.   NATURAL PRODUCT REPORTS

Glucosinolates: The synthetic approach

(2010) Patrick Rollin et al.   COMPTES RENDUS CHIMIE

The synthesis of novel hexa-13C-labelled glucosinolates from [13C6]-d-glucose

(2009) Qingzhi Zhang et al.   TETRAHEDRON