
Journal of the Chemical Society. Perkin transactions I p. 1521 - 1533 (1990)
Update date:2022-08-04
Topics:
Baggaley, Keith H.
Elson, Stephen W.
Nicholson, Neville H.
Sime, John T.
Proclavaminic acid (1) was synthesized by a route which indicated its constitution to be (2S,3R)-5-amino-3-hydroxy-2-(2-oxoazetidin-1-yl)valeric acid.The spectroscopic properties of the synthetic material were identical with those of natural proclavaminic acid, and, like the natural product, it was converted into clavaminic acid (2) by clavaminic acid synthase.An efficient synthesis of 3-hydroxyornithine derivatives was devised which allowed the separation of diastereoisomers and the resolution of a threo compound by the acylase
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