PIFA-mediated intramolecular <i>N</i>-arylation of 2-aminoquinoxalines to afford indolo[2,3-<i>b</i>]quinoxaline derivatives-Reference-Cited by-同舟云学术

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PIFA-mediated intramolecular N-arylation of 2-aminoquinoxalines to afford indolo[2,3-b]quinoxaline derivatives

Published:2024 Issue:28 Volume:22 Page:5803-5808
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Subramaniam Subhashini V.¹,Singh Badal¹,Pradeep Natarajan¹,Peruncheralathan Saravanan¹^ORCID

Affiliation:

1. School of Chemical Sciences, National Institute of Science Education and Research (NISER) Bhubaneswar, an OCC of Homi Bhabha National Institute, Khurda – 752050, India

Abstract

N-Arylation of aminoheteroarenes: room-temperature C–N bond formation in 2-amino-3-arylquinoxalines using a hypervalent iodine reagent unlocks a versatile pathway to indolo[2,3-b]quinoxalines.

Funder

Department of Atomic Energy, Government of India

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00812J

Reference44 articles.

1. Medicinal chemistry of indole derivatives: Current to future therapeutic prospectives

2. Polyindole and polypyrrole as a sustainable platform for environmental remediation and sensor applications

3. Indole-containing new types of dyes and their UV–vis and NMR spectra and electronic structures: Experimental and theoretical study

4. Quinoxaline, its derivatives and applications: A State of the Art review

5. A Review on Multipurpose Potential of Bioactive Heterocycle Quinoxaline

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