105748-60-5Relevant articles and documents
2-(Substituted phenyl)amino analogs of 1-methoxyspirobrassinol methyl ether: Synthesis and anticancer activity
Kutschy, Peter,Salayova, Aneta,Curillova, Zuzana,Kozar, Tibor,Mezencev, Roman,Mojzis, Jan,Pilatova, Martina,Balentova, Eva,Pazdera, Pavel,Sabol, Marian,Zburova, Michaela
, p. 3698 - 3712 (2009)
New analogs of indole phytoalexin 1-methoxyspirobrassinol methyl ether have been designed by replacement of its 2-methoxy group with 2-(substituted phenyl)amino group. Synthesized by spirocyclization methodology, trans- and cis-diastereoisomers of target
Sinalbins A and B, phytoalexins from Sinapis alba: Elicitation, isolation, and synthesis
Pedras, M.Soledade C,Zaharia, Irina L
, p. 213 - 216 (2000)
The chemical structure and synthesis of sinalbin A is described. This cruciferous phytoalexin is produced by white mustard (Sinapis alba) after treatment with biotic and abiotic elicitors. In addition, a related metabolite, named sinalbin B, is present in extracts from elicited plants, but not in those from non-elicited controls. Sinalbin B, which was also synthesized appears to be both a phytoalexin and a biosynthetic precursor of sinalbin A. (C) 2000 Elsevier Science Ltd.
A SIMPLE SYNTHESIS OF A PHYTOALEXIN, METHOXYBRASSININ
Somei, Masanori,Kobayashi, Kensuke,Shimizu, Kazuhisa,Kawasaki, Toshiya
, p. 77 - 80 (2007/10/02)
A simple and an alternative multi-gram scale synthetic method methoxybrassinin is developed starting from indole-3-carboxaldehyde.