AM1 study of structure-activity relationships in bicyclic aza-β-lactams

dc.contributor.author Nangia, A.
dc.contributor.author Chandrakala, P. S.
dc.contributor.author Balaramakrishna, M. V.
dc.contributor.author Latha, T. V.A.
dc.date.accessioned 2022-03-27T09:35:43Z
dc.date.available 2022-03-27T09:35:43Z
dc.date.issued 1995-11-10
dc.description.abstract AM1 calculations on bicyclic aza-β-lactams 4 (1,3-diazetidin-2-ones) are carried out to investigate the effect of ring size (five versus six), position of olefin (Δ2 versus Δ3), and electronegative atom (oxygen) in the tethered non-β-lactam ring on the structure of diazetidinone. The results are discussed in terms of structural trends related to β-lactamase and transpeptidase inactivation capability. The biological activity of novel aza-β-lactams 4 is comparable to that of β-lactams 3. © 1995.
dc.identifier.citation Journal of Molecular Structure: THEOCHEM. v.343(C)
dc.identifier.issn 01661280
dc.identifier.uri 10.1016/0166-1280(95)90547-2
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/0166128095905472
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13093
dc.title AM1 study of structure-activity relationships in bicyclic aza-β-lactams
dc.type Journal. Article
dspace.entity.type
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