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Pyrrolidine-2,3-diones: heterocyclic scaffolds that inhibit and eradicate S. aureus biofilms.
Valdes-Pena MA +4 more
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Easy approach to 3-benzylimino-2-pyrrolidinones from 3-chloro-4-chloromethyl-2-pyrrolidinones
Tetrahedron Letters, 1999Abstract 3-Benzylimino-2-pyrrolidinones can be prepared in good yield by heating 3-chloro-4-chloromethyl-2-pyrrolidinones, benzylamine and NaI in THF at 80°C. An endo -dehydrohalogenation followed by a SN 2 ′ substitution on the intermediate allyl chloride, and finally a shift of the exo -double bond to Δ 3 with attendant tautomerization ...
Franco Ghelfi +2 more
exaly +3 more sources
Lewis Base‐Catalysed Enantioselective Radical Conjugate Addition for the Synthesis of Enantioenriched Pyrrolidinones [PDF]
We report a catalytic asymmetric protocol for the preparation of chiral pyrrolidinones proceeding via a radical pathway. The chemistry exploits the combination of photoredox catalysis and Lewis base catalysis to realise the first example of asymmetric ...
Will C Hartley +2 more
exaly +3 more sources
3-Pyrrolidinones by Intramolecular Condensation
Journal of the American Chemical Society, 1964James. Blake +2 more
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Structural analysis of pyrrolidinones
Acta Crystallographica Section C Crystal Structure Communications, 2000In the course of a study on pyrrolidinones, the crystal structures of four compounds, namely, methyl N-[(4-methoxyphenyl)(3,4,5-trimethoxyphenyl)methyl]pyroglutamate, C23H27NO7, methyl N-[naphthyl-(3,4,5-trimethoxyphenyl)methyl]pyroglutamate diacetyl peroxide, C26H27NO6·-0.5C4H6O4, 5-(3,4,5-trimethoxyphenyl)-1,2,3,11b-tetrahydro-
Camus, Fabrice +5 more
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Studies on pyrrolidinones. A convenient synthesis of 5‐cyano‐2‐pyrrolidinone derivatives
Journal of Heterocyclic Chemistry, 1986AbstractThe reaction of 2‐pyrrolidinone‐5‐carboxamide (pyroglutamide) with trimethylchlorosilane and zinc chloride as a catalyst afford in one step a 91% yield of N‐trimethylsilylpyroglutamic acid nitrile whose acylation gives N‐acyl compounds 2b,c.
Benoǐt Rigo +2 more
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Unexpected reaction of β-cyclodextrin tosylate with pyrrolidinones
Carbohydrate Research, 2006Substitution reactions of 6I-O-p-tolylsulfonylcyclomaltoheptaose with alkyl- and arylamines in 1-methyl-2-pyrrolidinone and various pyrrolidinones were investigated. An unexpected reaction of the tosyl group with pyrrolidinones was observed resulting in products deriving from nucleophilic attack by the lactam carbonyl oxygen and further opening of the ...
CUZZOLA A. +5 more
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Optimization of pyrrolidinone based HIV protease inhibitors
Bioorganic & Medicinal Chemistry Letters, 2005Optimization of P1-substituted pyrrolidinone based HIV protease inhibitors has yielded analogs with very potent antiviral activity.
Ronald G, Sherrill +8 more
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Chemischer Informationsdienst, 1986
AbstractPyroglutamid (I) wird zu (II) silyliert und dann mit Zinkchlorid über (III) zum 5‐Cyan‐2‐pyrrolidinon (IVa) desilyliert.
B. RIGO, C. LESPAGNOL, M. PAULY
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AbstractPyroglutamid (I) wird zu (II) silyliert und dann mit Zinkchlorid über (III) zum 5‐Cyan‐2‐pyrrolidinon (IVa) desilyliert.
B. RIGO, C. LESPAGNOL, M. PAULY
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2009
[872-50-4] C5H9NO (MW 99.15) InChI = 1S/C5H9NO/c1-6-4-2-3-5(6)7/h2-4H2,1H3 InChIKey = SECXISVLQFMRJM-UHFFFAOYSA-N (special solvent;1 source of enolates2) Alternate Names: NMP; N-methylpyrrolidone. Physical Data: mp −24.4 °C; bp 202 °C; d 1.030 g cm−3.
Peteris Trapencieris, Julie A. Pigza
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[872-50-4] C5H9NO (MW 99.15) InChI = 1S/C5H9NO/c1-6-4-2-3-5(6)7/h2-4H2,1H3 InChIKey = SECXISVLQFMRJM-UHFFFAOYSA-N (special solvent;1 source of enolates2) Alternate Names: NMP; N-methylpyrrolidone. Physical Data: mp −24.4 °C; bp 202 °C; d 1.030 g cm−3.
Peteris Trapencieris, Julie A. Pigza
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