A versatile approach to (4S,5R)-4-benzyloxy-5-(α-hydroxyalkyl)-2-pyrrolidinones: Experimental evidences to the computational predictions [PDF]
Jian-Liang Ye+3 more
core +1 more source
Improved synthesis and comparative analysis of the tool properties of new and existing D-ring modified (S)-blebbistatin analogs [PDF]
Bracke, Marc+3 more
core +2 more sources
Ring transformation of tetrahydrofuran into tetrahydrophiopene over alkali metal cation exchanged zeolites [PDF]
Hatada, K., Mori, T., Ono, Y.
core
Polychlorinated pyrrolidinones from a Saudi Arabian Red Sea sponge of the genus Lamellodysidea [PDF]
Agusti Susana+4 more
core
Studies on Pyrrolidinones: Chemistry of Dimethoxytriazines [PDF]
AbstractThe synthesis of 3,5‐dimethoxy‐1,3,5‐triazines (III) is developed: demethylation and N‐methylation of these products is studied.
Benoît Rigo+6 more
openaire +2 more sources
Thermodynamic and spectroscopic properties of 2-pyrrolidinones. 2. Dielectric properties of 2-pyrrolidinone in binary mixtures [PDF]
Dielectric permittivities of 2-pyrrolidinone - acetone, -dimethyl sulfoxide,-2-propanol, -dichloromethane and -water systems were measured as a function of mole fraction over the whole composition range at 30 and 50°C. The excess dielectric permittivities are predominantly negative for all the mixtures and the excess molar polarizations are negative ...
Päivi L. Pirilä-Honkanen, P. Ruostesuo
openaire +1 more source
Related searches:
Structural analysis of pyrrolidinones
Acta Crystallographica Section C Crystal Structure Communications, 2000AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
François Durant+5 more
openaire +5 more sources
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.
B. Rigo, Marc Pauly, Charles Lespagnol
openaire +2 more sources
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
openaire +7 more sources