Abstract
(R)-alpha-Aminoadipic acid is available on a large scale by enzymatic cleavage from cephalosporin C (CephC) in the production of 7-aminocephalosporanic acid (7-ACA). It can be converted into other interesting enantiomerically pure compounds, e. g. derivatives of (R)-pipecolic acid (R-piperidine-2-carboxylic acid), (R)-6-oxopiperidine-2-carboxylic acid, (R)-1,2,3,4-tetrahydropyridine-2(2H)-carboxylates, and other compounds obtained by further conversions of these products.
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