Regioselective synthesis of functionalized [1,8]naphthyridine derivatives via three-component domino reaction under catalyst-free conditions-Reference-Cited by-同舟云学术

Regioselective synthesis of functionalized [1,8]naphthyridine derivatives via three-component domino reaction under catalyst-free conditions

Published:2015 Issue:2 Volume:17 Page:973-981
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Feng Xian¹²³⁴⁵,Wang Jian-Jun¹²³⁴⁵,Zhang Juan-Juan¹²³⁴⁵,Cao Cheng-Pao¹²³⁴⁵,Huang Zhi-Bin¹²³⁴⁵,Shi Da-Qing¹²³⁴⁵

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province

2. College of Chemistry

3. Chemical Engineering and Materials Science

4. Soochow University

5. Suzhou 215123

Abstract

The advantages of this protocol are short reaction times, catalyst-free conditions, cheap and benign solvents, and high regio- and stereo-selectivities.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/GC/C4GC01469C

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4. Synthesis, Inhibitory Activity of Cholinesterases, and Neuroprotective Profile of Novel 1,8-Naphthyridine Derivatives

5. Antimycobacterial Activities of Novel 1-(Cyclopropyl/tert-butyl/4-fluorophenyl)-1,4-dihydro- 6-nitro-4-oxo-7-(substituted secondary amino)-1,8-naphthyridine-3-carboxylic Acid

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