Asymmetric synthesis, characterization of chiral trans and cis-3-chloro/oxo/thio-4-styryl--lactams using (R)-(+)-1-phenylethylamine and their efficient column chromatographic separation

Diverse chiral trans and cis-3-chloro/oxo/thio-4-styryl-beta-lactams were efficiently synthesized using chiral 3 '-phenylallylidene-[(R)-1 ' -phenylethyl] amine and substituted ethanoic acids. Moore ketenes derived from chloro/phenythio/benzylthio ethanoic acids (Cl/PhS/BzS) affords both chiral trans- and cis beta-lactams, with a preference for trans-stereochemistry. However, Bose-Evans ketenes obtained from 2-methoxy/phenoxyethanoic acids (MeO/PhO), led to the exclusive formation of cis-diastereomers only. Further, individual diastereomers of trans- and cis-beta-lactams were separated via efficient column chromatography. The relative cis and trans configuration of the C-3 and C-4 protons in chiral beta-lactams was established using coupling constant value ranging from J = 1.4 to 2.1 Hz (in case of trans) and J = 4.3 to 5.2 Hz (in case of cis) respectively. Structural confirmation of beta-lactams was done using FT-IR, NMR (1H,13C,1H-1H COSY and 1H-13C HSQC), elemental analysis, ESI-MS and X-ray crystallography. [GRAPHICS]