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Chem Biodivers ; 19(1): e202100584, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34752012

ABSTRACT

Synthesis of novel C3-substituted 5,6-dihydropyrrolo[2,1-a]isoquinolines via a three-component domino reaction of 1-aroyl-3,4-dihydroisoquinolines, terminal alkynes and CH-acids under microwave irradiation in dry acetonitrile is described. The method developed enables the obtainment of highly functionalized compounds with pharmacophore groups, which are potentially biologically active.


Subject(s)
Isoquinolines/chemistry , Pyrroles/chemistry , Alkynes/chemistry , Cycloaddition Reaction , Isoquinolines/chemical synthesis , Magnetic Resonance Spectroscopy , Microwaves , Molecular Conformation , Pyrroles/chemical synthesis
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