Efficient synthesis of novel N-substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation reaction-Reference-Cited by-同舟云学术

Efficient synthesis of novel N-substituted 2-carboxy-4-quinolones via lithium bis(trimethylsilyl)amide (LiHMDS)-induced in situ cyclocondensation reaction

Published:2017 Issue:19 Volume:7 Page:11367-11372
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Hasan Phool¹²³⁴⁵,Aneja Babita¹²³⁴⁵,Masood Mir M.¹²³⁴⁵,Ahmad Md. Belal⁶⁷⁸⁹⁵,Yadava Umesh¹⁰¹¹¹²⁵,Daniliuc Constantin G.¹³¹⁴¹⁵,Abid Mohammad¹²³⁴⁵^ORCID

Affiliation:

1. Medicinal Chemistry Lab

2. Department of Biosciences

3. Jamia Millia Islamia

4. New Delhi 110025

5. India

6. Department of Chemistry

7. TNB College

8. TM Bhagalpur University

9. Bhagalpur 812007

10. Department of Physics

11. Deen Dayal Upadhyay Gorakhpur University

12. Gorakhpur

13. Organisch-Chemisches Institut

14. Westfälische Wilhelm-Universität Münster

15. Germany

Abstract

Efficient synthesis ofN-aryl-2-carboxy-substituted 4-quinolones with broad substrate scope and high regioselectivity.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C6RA28631C

Reference34 articles.

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2. Synthesis of 6-aryl substituted 4-quinolones via Suzuki cross coupling

3. Synthesis and cytotoxicity of 1,6,7,8-substituted 2-(4'-substituted phenyl)-4-quinolones and related compounds: identification as antimitotic agents interacting with tubulin

4. Antimitotic Activity of 5-Hydroxy-7-methoxy-2-phenyl-4-quinolones

5. Cancer preventive agents, Part 2: Synthesis and evaluation of 2-phenyl-4-quinolone and 9-oxo-9,10-dihydroacridine derivatives as novel antitumor promoters

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