2018
DOI: 10.1016/j.ica.2018.03.028
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Stereoselective synthesis, spectroscopic and X-ray crystallographic characterization of novel trans- and cis-3-methylseleno substituted monocyclic β-lactams: Potential synthons for C-3 functionalized/bicyclic/halospiroseleno-β-lactams of medicinal interest

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Cited by 8 publications
(1 citation statement)
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“…e imine employed in this work has been used for several purposes. For instance, Bhalla et al [6] reported the synthesis of novel trans-and cis-3methylseleno substituted β-lactams through Staudinger cycloaddition reaction between the Schiff's bases and ketene generated from 2-methylselenoethanoic acid. Cai et al [7] designed and synthesized some 50 N-benzylideneaniline compounds and carried out in vitro studies on the inhibitory activity in human HEK-Blue TLR2 cells.…”
Section: Introductionmentioning
confidence: 99%
“…e imine employed in this work has been used for several purposes. For instance, Bhalla et al [6] reported the synthesis of novel trans-and cis-3methylseleno substituted β-lactams through Staudinger cycloaddition reaction between the Schiff's bases and ketene generated from 2-methylselenoethanoic acid. Cai et al [7] designed and synthesized some 50 N-benzylideneaniline compounds and carried out in vitro studies on the inhibitory activity in human HEK-Blue TLR2 cells.…”
Section: Introductionmentioning
confidence: 99%