Synthesis of 1,3-diazetidin-2-ones (aza-β-lactams) as rationally designed transpeptidase and β-lactamase inhibitors

dc.contributor.author Nangia, A.
dc.contributor.author Chandrakala, P. S.
dc.date.accessioned 2022-03-27T09:35:46Z
dc.date.available 2022-03-27T09:35:46Z
dc.date.issued 1995-10-16
dc.description.abstract Pyrimidinone 4 is converted to diazetidinone carboxaldehyde 6. Selective chemical transformations on tricarbonyl substrate 6 with different reagents are performed. Synthon 6 is employed as a versatile template for elaboration to bicyclic diazetidinones 7, 12 and 15. A novel class of aza-β-lactam compounds are synthesised as potential transpeptidase and β-lactamase inhibitors. © 1995 Pergamon Elsevier Science Ltd.
dc.identifier.citation Tetrahedron Letters. v.36(42)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/0040-4039(95)01473-U
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/004040399501473U
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13094
dc.title Synthesis of 1,3-diazetidin-2-ones (aza-β-lactams) as rationally designed transpeptidase and β-lactamase inhibitors
dc.type Journal. Article
dspace.entity.type
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