The efficient, enantioselective synthesis of quinoxaline, pyrazine and 1,2,4-triazine substituted α-amino acids from vicinal tricarbonyls
Adlington, Robert M.; Baldwin, Jack E.; Catterick, David; Pritchard, Gareth J.; Adlington Robert M.; The Dyson Perrins Laboratory, University of Oxford; Baldwin Jack E.; The Dyson Perrins Laboratory, University of Oxford; Catterick David; The Dyson Perrins Laboratory, University of Oxford; Pritchard Gareth J.; The Dyson Perrins Laboratory, University of Oxford
Журнал:
Journal of the Chemical Society, Perkin Transactions 1
Дата:
2001
Аннотация:
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 of heterocyclic amino acid systems.
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