80656-34-4Relevant articles and documents
Deconjugation of dehydroamino acids: Stereoselective synthesis of racemic (E)-vinylglycines
Alexander, Paul A.,Marsden, Stephen P.,Munoz Subtil, Dulce M.,Reader, John C.
, p. 5433 - 5436 (2007/10/03)
(Chemical Equation Presented) A practical and general two-step synthesis of carbamate-protected (E)-vinylglycines from aliphatic aldehydes is reported. The key step involves the kinetic α-protonation of dianionic dienolates derived from dehydroamino acids
A flexible synthesis of azasugars and homoazasugars via olefin metathesis
Huwe, Christoph M.,Blechert, Siegfried
, p. 61 - 67 (2007/10/03)
A flexible synthesis of azasugars and homoazasugars from vinyl glycine methyl ester is described. The syntheses, which are based on ring closing olefin metathesis steps and stereocontrolled functionalizations of the formed double bonds, offer a broad vari
Structure and Stereochemistry of Three Phytotoxins, Syringomycin, Syringotoxin and Syringostatin, Produced by Pseudomonas syringae pv. syringae
Fukuchi, Naoyuka,Isogai, Akira,Nakayama, Jiro,Takayama, Seiji,Yamashita, Shuichi,et al.
, p. 1149 - 1158 (2007/10/02)
The structures of two phytotoxins, syringomycin and syringotoxin, produced by Pseudomonas syringae pv. syringae, were determined.Several amino acid residues of syringomycin were different from those in the syringostatins.Syringotoxin B proved to be syringostatin A.The three kinds of phytotoxins showed close structural similarity, and the stereochemistry of their components was deduced and compared.