2022
DOI: 10.1080/17518253.2022.2064194
|View full text |Cite
|
Sign up to set email alerts
|

A review on synthetic investigation for quinoline- recent green approaches

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
16
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 32 publications
(16 citation statements)
references
References 128 publications
0
16
0
Order By: Relevance
“…DABCO is a cagelike tertiary amine having weak alkalinity. This cagelike structure increases the energy barrier of nitrogen inversion so the lone pair is localized and makes DABCO more susceptible toward quaternization and ionic liquid preparation and further applied in organic reactions. Regarding the abovementioned notable properties of 1,4-DHP derivatives, their synthetic methods have been investigated in various environmental conditions. However, most of the research studies have been done on the synthesis of 3-carboxylate derivatives of 1,4,5,6,7,8-hexahydroquinoline compared to 3-carbonitrile derivatives. 1,4,5,6,7,8-Hexahydroquinoline-3-carbonitrile was previously synthesized using NH 4 OAc, sulfonated rice husk, nanosized MgO, nano-Fe 3 O 4 @TDI@TiO 2 , citric acid/MCM-48, and K 2 CO 3 catalyst. Despite the undeniable advantages of these processes, some disadvantages are also present, like the involvement of metal catalysts, nonrecyclable catalysts, high catalyst loading, long reaction time, high temperature, and small substrate scope.…”
Section: Introductionmentioning
confidence: 99%
“…DABCO is a cagelike tertiary amine having weak alkalinity. This cagelike structure increases the energy barrier of nitrogen inversion so the lone pair is localized and makes DABCO more susceptible toward quaternization and ionic liquid preparation and further applied in organic reactions. Regarding the abovementioned notable properties of 1,4-DHP derivatives, their synthetic methods have been investigated in various environmental conditions. However, most of the research studies have been done on the synthesis of 3-carboxylate derivatives of 1,4,5,6,7,8-hexahydroquinoline compared to 3-carbonitrile derivatives. 1,4,5,6,7,8-Hexahydroquinoline-3-carbonitrile was previously synthesized using NH 4 OAc, sulfonated rice husk, nanosized MgO, nano-Fe 3 O 4 @TDI@TiO 2 , citric acid/MCM-48, and K 2 CO 3 catalyst. Despite the undeniable advantages of these processes, some disadvantages are also present, like the involvement of metal catalysts, nonrecyclable catalysts, high catalyst loading, long reaction time, high temperature, and small substrate scope.…”
Section: Introductionmentioning
confidence: 99%
“…4 Acetic acid is also used as a green solvent at high temperatures for pyridine derivative synthesis. 43 There are not many systems available that are more viable in terms of environmental protection and atom economy. Among the nitrogen heterocyclic compounds, aminocyanohydropyridine derivatives are important motifs for organic synthesis and are widely found in many natural products, having different biological activities such as antimicrobial agents, 44 anticancer agents, 45 psychotropic, 46 anti-allergenic, 46 anti-inflammatory, 46 and estrogenic activities, and MK-2 kinase inhibitors 7 (Fig.…”
Section: Introductionmentioning
confidence: 99%
“…4 Acetic acid is also used as a green solvent at high temperatures for pyridine derivative synthesis. 43 There are not many systems available that are more viable in terms of environmental protection and atom economy.…”
Section: Introductionmentioning
confidence: 99%
“…There is a plethora of classical reactions such as Gould–Jacob, Friedländer, Pfitzinger, Skraup, Doebner–von Miller, and Conrad–Limpach for accessing quinoline and its derivatives . Apart from these methods, a number of transition metal catalyzed approaches and green protocols were also developed . In this letter, we describe a new approach to synthesize 3-aroyl/acyl quinolines.…”
Section: Introductionmentioning
confidence: 99%