Electricity-driven, oxidative C–H selenylative and tellurylative annulation of <i>N</i>-(2-alkynyl)anilines: sustainable synthesis of 3-selanyl/tellanylquinolines-Reference-Cited by-同舟云学术

Electricity-driven, oxidative C–H selenylative and tellurylative annulation of N-(2-alkynyl)anilines: sustainable synthesis of 3-selanyl/tellanylquinolines

Published:2024 Issue:55 Volume:60 Page:7057-7060
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Naresh Ainala¹,Keerthana H. Sai¹,Mukherjee Nilanjana¹,Chatterjee Tanmay¹^ORCID

Affiliation:

1. Department of Chemistry, Birla Institute of Technology and Science, Pilani (BITS Pilani), Hyderabad Campus, Jawahar Nagar, Kapra Mandal, Hyderabad-500078, Telangana, India

Abstract

A metal- and oxidant-free, electricity-driven C–H selenylative and tellurylative annulation of N-(2-alkynyl)anilines with diorganyl dichalcogenides is developed to access 3-chalcogenylquinolines.

Funder

Council of Scientific and Industrial Research, India

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC01780C

Reference37 articles.

1. Quinoline, quinazoline and acridone alkaloids

2. Quinoline as a Privileged Scaffold in Cancer Drug Discovery

3. Synthesis and biological evaluation of quinoline analogues of flavones as potential anticancer agents and tubulin polymerization inhibitors

4. Synthetic and medicinal perspective of quinolines as antiviral agents

5. Quinoline: A Promising Scaffold in Recent Antiprotozoal Drug Discovery

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