Lewis acid-mediated modular route to the synthesis of 3-substituted quinolines from 2-aminobenzyl alcohols and enamine(one)s-Reference-Cited by-同舟云学术

Lewis acid-mediated modular route to the synthesis of 3-substituted quinolines from 2-aminobenzyl alcohols and enamine(one)s

Published:2024 Issue:15 Volume:48 Page:6902-6910
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Ghosh Aritra¹²,Upadhyay Samridhi¹,Dahatonde Dipak J.¹,Kant Ruchir³,Batra Sanjay¹²^ORCID

Affiliation:

1. Medicinal and Process Chemistry Division, CSIR- Central Drug Research Institute, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow-226031, Uttar Pradesh, India

2. Academy of Scientific and Innovative Research, CSIR-Human Resource Development Centre, (CSIR-HRDC), Campus Sector 19, Kamla Nehru Nagar, Ghaziabad, 201002, Uttar Pradesh, India

3. Molecular and Structural Biology Division, CSIR- Central Drug Research Institute, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow-226031, Uttar Pradesh, India

Abstract

A Lewis acid-mediated modular synthesis of 3-substituted quinolines bearing electron-withdrawing groups from readily available 2-aminobenzyl alcohols and N,N′-dimethylenamine(one)s is described.

Funder

Central Drug Research Institute

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NJ/D3NJ05556F

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