Diastereospecific arylation and cascade deconstructive amidation/thioesterification of readily available lactam-fused bromolactones. [PDF]
RSC Adv, 2023 Do M, Anosike SI, Beng TK.
europepmc +1 more source
BAL 9141, a new broad-spectrum pyrrolidinone cephalosporin: activity against clinically significant anaerobes in comparison with 10 other antimicrobials [PDF]
, 2002 Mandy Wootton
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ChemElectroChem, Volume 12, Issue 8, April 14, 2025.The study investigates suppressing polysulfide dissolution using a 1,3‐dioxolane (DOL) and nonpolar hydrocarbon mixture with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). Compared to the conventional 1 M LiTFSI in DOL/DME (50 : 50 v/v), the DOL/hydrocarbon electrolytes, especially DnH40LiTFSI (with n‐hexane), exhibit superior cycling stability ...
Faiz Ahmed, Defu Li, Gao Liu
wiley +1 more source
In Vitro Activities of BAL9141, a Novel Broad-Spectrum Pyrrolidinone Cephalosporin, against Gram-Negative Nonfermenters [PDF]
, 2002 Reinhard Zbinden +2 more
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Bactericidal activity and synergy studies of BAL9141, a novel pyrrolidinone-3-ylidenemethyl cephem, tested against streptococci, enterococci and methicillin-resistant staphylococci [PDF]
, 2003 Lalitagauri M. Deshpande +1 more
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Pyrrolidinones as Modulators of Neurogenesis [PDF]
ACS Medicinal Chemistry Letters, 2016 openaire +3 more sources
Phase behavior of poly(ether imide) in mixtures of N-methyl-2-pyrrolidinone and methylene chloride [PDF]
, 2003 Tai‐Horng Young +2 more
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Expeditious Approach to 5‐Aroyl‐pyrrolidinones by a Novel PIFA‐Mediated Alkyne Amidation Reaction. [PDF]
, 2005 Sonia Serna +4 more
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Synthesis of New Polysubstituted Pyrrolidinones with Potential Biological Activity [PDF]
, 2008 Nikola Burdzhiev, Elena Stanoeva
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From Conventional to Sustainable Catalytic Approaches for Heterocycles Synthesis [PDF]
Synthesis of heterocyclic compounds is fundamental for all the research area in chemistry, from drug synthesis to material science. In this framework, catalysed synthetic methods are of great interest to effective reach such important building blocks. In
Buscemi S. +4 more
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