Assembling the biosynthetic puzzle of crucifer metabolites: indole-3-acetaldoxime is incorporated efficiently into phytoalexins but glucobrassicin is not

Assembling the biosynthetic puzzle of crucifer metabolites: indole-3-acetaldoxime is incorporated efficiently into phytoalexins but glucobrassicin is not Two natural indole glucosinolates from Brassicaceae Cancer chemopreventive activity of brassinin, a phytoalexin from cabbage Biosynthesis of 2-hydroxy-3-butenylglucosinolate and 3-butenylglucosinolate in Brassica napus 1,4-Dimethoxyglucobrassicin in <i>Barbarea</i> and 4-Hydroxyglucobrassicin in <i>Arabidopsis</i> and <i>Brassica</i> Cyclobrassinin sulphoxide, a sulphur-containing phytoalexin from Brassica juncea Brassinin oxidase mediated transformation of the phytoalexin brassinin: Structure of the elusive co-product, deuterium isotope effect and stereoselectivity Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in <i>Arabidopsis</i> Brassicanals A and B, Novel Sulfur-Containing Phytoalexins from the Chinese Cabbage <i>Brassica campestris</i> L. ssp. <i>pekinensis</i> The phytopathogenic fungus Alternaria brassicicola: Phytotoxin production and phytoalexin elicitation