2014
DOI: 10.1016/j.tetlet.2013.11.105
|View full text |Cite
|
Sign up to set email alerts
|

Choline chloride/CuCl as an effective homogeneous catalyst for palladium-free Sonogashira cross-coupling reactions

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
24
0

Year Published

2014
2014
2020
2020

Publication Types

Select...
6
3

Relationship

1
8

Authors

Journals

citations
Cited by 51 publications
(25 citation statements)
references
References 22 publications
0
24
0
Order By: Relevance
“…The one-pot reaction of various aromatic aldehydes, ketones, aliphatic amines, and carbon disulfide, in the presence of potassium hydroxide in ChCl/urea at room temperature, led to the corresponding dithiocarbamates (138) in good to excellent yields (Scheme 51). The one-pot reaction of various aromatic aldehydes, ketones, aliphatic amines, and carbon disulfide, in the presence of potassium hydroxide in ChCl/urea at room temperature, led to the corresponding dithiocarbamates (138) in good to excellent yields (Scheme 51).…”
Section: Scheme 50mentioning
confidence: 99%
“…The one-pot reaction of various aromatic aldehydes, ketones, aliphatic amines, and carbon disulfide, in the presence of potassium hydroxide in ChCl/urea at room temperature, led to the corresponding dithiocarbamates (138) in good to excellent yields (Scheme 51). The one-pot reaction of various aromatic aldehydes, ketones, aliphatic amines, and carbon disulfide, in the presence of potassium hydroxide in ChCl/urea at room temperature, led to the corresponding dithiocarbamates (138) in good to excellent yields (Scheme 51).…”
Section: Scheme 50mentioning
confidence: 99%
“…40 Besides, DESs have been known as preferable alternative solvents/catalysts for organic synthesis due to their non-hazardous, non-toxic, stable, non-ammable, and inexpensive nature. [41][42][43][44][45][46][47][48][49] Recently, we have reported DESs-catalyzed organic transformations such as Friedel-Cras acylation and esterication of sterically hindered alcohols. 50,51 As our ongoing efforts to develop environmentally benign syntheses, it is the aim of this communication to describe our preliminary results in the arylation of benzoxazoles with aromatic aldehyde using DES as a green catalyst.…”
Section: Introductionmentioning
confidence: 99%
“…Add to this, ChCl:CuCl DESs became attractive homogeneous catalysts in view of their ease of applications and low costs in the palladium-free Sonogashira-type cross-coupling reactions. The use of this catalyst led to the formation of substituted aromatic alkynes in excellent yields about 97% under palladium-free conditions [17]. Besides, the electrochemical screening of both ammonium and phosphonium-based DESs on the potential applications of redox flow batteries was conducted.…”
Section: Introductionmentioning
confidence: 99%
“…It was observed that DESs synthesized from ammonium salts provided a larger potential window in comparison to the phosphonium-based counterparts [18]. In addition, ChCl-based DESs were utilized by different groups as an electrolyte in lithium ion batteries, electric double layer capacitors, and as electrolytic media in electropolishing of metals [17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%