The efficient, enantioselective synthesis of quinoxaline, pyrazine and 1,2,4-triazine substituted α-amino acids from vicinal tricarbonyls
The reaction of diamines and amidrazones with α-amino acid vicinal tricarbonyls has been shown to be a versatile route towards novel heterocyclic α-amino acids. This route is also applicable to parallel synthesis and has allowed the formation of a range o
Adlington,Baldwin,Catterick,Pritchard
p. 668 - 679
(2007/10/03)
A versatile synthetic route to quinoxaline, pyrazine and 1,2,4-triazine substituted α-amino acids from vicinal tricarbonyls
A range of novel heterocyclic α-amino acids has been synthesised by the reaction of diamines and amidrazones with α-amino acid vicinal tricarbonyl reactive substrates. The Royal Society of Chemistry 2000.
Adlington, Robert M.,Baldwin, Jack E.,Catterick, David,Pritchard, Gareth J.
p. 299 - 302
(2007/10/03)
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