Novel (±)- trans- β-lactam ureas: Synthesis, in silico and in vitro biological profiling
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A diastereomeric mixture of racemic 3-phthalimido-b-lactam 2a/2b was synthesized by the Staudinger reaction of carboxylic acid activated with 2-chloro-1-methylpyridinium iodide and imine 1. The amino group at the C3 position of the b-lactam ring was used for f... ...
