Total synthesis of a nuclear analogue of the penicillin–cephalosporin antibiotics

Abstract
A synthetic route has been developed for the preparation of nuclear analogues of the penicillin–cephalosporin group of antibiotics and is illustrated by the synthesis of (2R,6R,7S)-8-oxo-7-phenylacetamido-1-azabicyclo[4,2,0]octane-2-carboxylic acid (17) from D-pipecolic acid.

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