Three-component synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines from 1-aroyl-3,4-dihydroisoquinolines, electron-deficient alkynes and NH-acids-Reference-Cited by-同舟云学术

Three-component synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines from 1-aroyl-3,4-dihydroisoquinolines, electron-deficient alkynes and NH-acids

Published:2022-08 Issue: Volume:103 Page:153991
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Miftyakhova Almira R.,Sidakov Matvey B.,Borisova Tatiana N.,Ilyushenkova Valentina V.,Fakhrutdinov Artem N.,Sorokina Elena A.,Varlamov Alexey V.,Voskressensky Leonid G.

Funder

RUDN University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference29 articles.

1. Another Facet to the Anticancer Response to Lamellarin D: Induction of Cellular Senescence through Inhibition of Topoisomerase I and Intracellular Ros Production

2. Synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines featuring an intramolecular radical-oxidative cyclization of polysubstituted pyrroles, and evaluation of their cytotoxic activity

3. Homobivalent Lamellarin-Like Schiff Bases: In Vitro Evaluation of Their Cancer Cell Cytotoxicity and Multitargeting Anti-Alzheimer’s Disease Potential

4. Oxidative Dearomatization of 4,5,6,7-Tetrahydro-1H-indoles Obtained by Metal- and Solvent-Free Thermal 5-endo-digCyclization: The Route to Erythrina and Lycorine Alkaloids

5. Efficient Formal Total Synthesis of the Erythrina Alkaloid (+)-Erysotramidine, Using a Domino Process

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