Stereoselective synthesis and characterization of monocyclic cis‐ β‐lactams containing 5‐methyl‐1,3,4‐thiadiazole‐2‐thiol moiety
Author:
Affiliation:
1. Department of Chemistry National Institute of Technology Patna Patna India
Publisher
Wiley
Subject
Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4344
Reference68 articles.
1. Design, synthesis and biological evaluation of some novel diastereoselective β-lactams bearing 2-mercaptobenzothiazole and benzoquinoline
2. Neuere Entwicklungen auf dem Gebiet der β-Lactam-Antibiotica
3. Synthesis and biological evaluation of some novel diastereoselective benzothiazole β-lactam conjugates
4. Green route for the heterocyclization of 2-mercaptobenzimidazole into β-lactum segment derivatives containing –CONH– bridge with benzimidazole: Screening in vitro antimicrobial activity with various microorganisms
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1. Functionalization of 2-Mercapto-5-methyl-1,3,4-thiadiazole: 2-(ω-Haloalkylthio) Thiadiazoles vs. Symmetrical Bis-Thiadiazoles;Molecules;2024-04-24
2. Designed synthetic pathway of stereoselective novel monocyclic cis‐bis‐β‐lactams including a 1,3,4‐thiadiazole‐2,5‐dithiol constituent: Antimicrobial activity, molecular docking;Journal of Heterocyclic Chemistry;2023-04-15
3. Stereoselective synthesis of β-lactams: recent examples;Organic & Biomolecular Chemistry;2023
4. Four-membered ring systems;Progress in Heterocyclic Chemistry;2023
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