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Radical Arylations
(John Wiley & Sons Ltd, 2012)
This chapter reports on radical arylations also highlighting the very important early achievements on this chemistry. To be named at this place are the Meerwein arylation and the Pschorr reaction. Intramolecular homolytic ...
Synthesis and characterization of a poly alkyl-aryl by Friedel-Crafts alkylation
(1994)
The synthesis of an alkyl-aryl prepolymer by a modified Friedel-Crafts alkylation is reported in the study. The influence of the concentration of the reactants on the physical properties and structure of the prepolymer and ...
Synthesis and characterization of a poly alkyl-aryl by Friedel-Crafts alkylation
(1994)
The synthesis of an alkyl-aryl prepolymer by a modified Friedel-Crafts alkylation is reported in the study. The influence of the concentration of the reactants on the physical properties and structure of the prepolymer and ...
Aryl-2 et alkyl-2 quinoléines nouvelles isolées d'une rutacée bolivienne : Galipea longiflora
(Can. J. of Chem., 1989)
Cinq aryl-2 et alkyl-2 quinoléines nouvelles ont été isolées des écorces de tiges de Galipea longiflora Krause (Rutacées) : la phényl-2 quinoléine 1, la (méthylènedioxy-3', 4') phénéthyl-2 quinoléine 2, la (diméthoxy-3',4') ...
P2O5/SiO2 : A Simple and Effective Catalyst for the Synthesis of N-substituted 1-Alkyl and 1-Aryl 3-Aminoisoquinolines
(Bentham Science Publishers, 2013-04)
A synthesis of N-substituted 1-alkyl and 1-aryl 3-aminoisoquinolines by cyclocondensation of 2- acylphenylacetonitriles with aliphatic and aromatic amines using P2O5/SiO2 as catalysts is described. Selectivity, simplicity ...
Microwave-induced Synthesis of N-Substituted 1-Alkyl and 1-Aryl 3-Aminoisoquinolines
(Bentham Science Publishers, 2017-03)
Background: Aminoisoquinolines are an important class of heterocyclic compounds. These compounds present a wide range of pharmacological properties including antimalaric, anticonvulsant and anti-inflammatory. Although ...
Gama-Lactones from Iryanthera species
(Elsevier B.V., 1983-12-01)
The structure of juruenolide, a constituent of Iryanthera juruensis and I. ulei is revised to (2S, 3R, 4S)-3-hydroxy-4-methyl-2-(19′-piperonyl-1′-n-nonadecyl)-butanolide. The compound is epimeric at C-3 of the γ-lactone ...