2014
DOI: 10.1039/c3ra45298k
|View full text |Cite
|
Sign up to set email alerts
|

CuO nanoparticle catalysed synthesis of 2H-indazoles under ligand free conditions

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
25
0

Year Published

2014
2014
2023
2023

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 36 publications
(25 citation statements)
references
References 32 publications
0
25
0
Order By: Relevance
“…The 2H -indazoles 5 – 8 were synthesised using a two-step approach including a Schiff base formation followed by intramolecular cyclisation 13 , 14 using microwave irradiation to reduce the reaction time of each step from 12 h to a few minutes. The condensation of aniline with 2-bromobenzaldehyde in presence of MgSO 4 under microwave activation allowed access to imine 1 – 4 in excellent yields.…”
Section: Resultsmentioning
confidence: 99%
“…The 2H -indazoles 5 – 8 were synthesised using a two-step approach including a Schiff base formation followed by intramolecular cyclisation 13 , 14 using microwave irradiation to reduce the reaction time of each step from 12 h to a few minutes. The condensation of aniline with 2-bromobenzaldehyde in presence of MgSO 4 under microwave activation allowed access to imine 1 – 4 in excellent yields.…”
Section: Resultsmentioning
confidence: 99%
“…White solid; yield: 1.80 g (93%); mp 81-82°C (Lit. 16 2-(4-methoxyphenyl)-2H-indazole (4b) [16]. Brown solid; yield: 2.04 g (91%); mp 132-133°C (Lit.…”
Section: Recovery Of the Catalystmentioning
confidence: 99%
“…Thus, the development of efficient and applicable methods for selective synthesis of 2 H ‐indazoles is of great significance to synthetic chemists. To overcome the problem of selectivity, several promising approaches have been developed in recent years . Although, a plenty of these procedure are useful and efficient; however, they are usually accompanied by one or more drawbacks such as long reaction times, the formation of regioisomers, requirement for expensive ligands, and limited substrate scope.…”
Section: Introductionmentioning
confidence: 99%
“…[1,[42][43][44][45][46][47][48][49][50][51][52][53][54] A common way for the formation of highly regioselective 2H-indazoles is based on the intramolecular coupling of properly pre-functionalized substrates including 2halobenzaldehydes. [55][56][57][58][59][60] This eco-efficient one-pot approach includes consecutive CÀ N and NÀ N bonds formation with extrusion of N 2 to corresponding 2H-indazoles.…”
Section: Introductionmentioning
confidence: 99%