Harnessing the benzyne insertion consequence to enable π-extended pyrido-acridine and quinazolino-phenanthridine-Reference-Cited by-同舟云学术

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Harnessing the benzyne insertion consequence to enable π-extended pyrido-acridine and quinazolino-phenanthridine

Published:2024 Issue:27 Volume:22 Page:5591-5602
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Ghosh Swarnali¹,Das Dwaipayan¹^ORCID,Mandal Rahul Dev¹^ORCID,Das Asish R.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Calcutta, 92, A. P. C. Road, Kolkata-700009, India

Abstract

Protocols have been devised for π-extended pyrido-acridines and quinazolino-phenanthridines, applying Rh(iii)- and Pd(ii)-mediated catalytic courses. The parent compounds are realized from 2-aminobenzonitrile and apposite benzyne precursor respectively.

Funder

University of Calcutta

University Grants Commission

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00533C

Reference42 articles.

1. Recent developments in the synthesis and biological activity of acridine/acridone analogues

2. Homobivalent Quinazolinimines as Novel Nanomolar Inhibitors of Cholinesterases with Dirigible Selectivity toward Butyrylcholinesterase

3. Marine Pyridoacridine Alkaloids: Biosynthesis and Biological Activities

4. Cationic π-extended heteroaromatics via a catalytic C–H activation annulative alkyne-insertion sequence

5. Recent Advances in Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds

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