2016
DOI: 10.1016/j.tetlet.2016.02.068
|View full text |Cite
|
Sign up to set email alerts
|

A microwave-assisted multicomponent protocol for the synthesis of benzofuran-2-carboxamides

Abstract: Radi, M. (2016). A microwave-assisted multicomponent protocol for the synthesis of benzofuran-2-carboxamides. TETRAHEDRON LETTERS. DOI: 10.1016DOI: 10. /j.tetlet.2016 Citing this paper Please note that where the full-text provided on King's Research Portal is the Author Accepted Manuscript or Post-Print version this may differ from the final Published version. If citing, it is advised that you check and use the publisher's definitive version for pagination, volume/issue, and date of publication details. And … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
7
0

Year Published

2016
2016
2022
2022

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 15 publications
(7 citation statements)
references
References 40 publications
0
7
0
Order By: Relevance
“…Radi et al succeeded in achieving substituted benzofuran-2-carboxamides via microwave assisted multi-component reaction of anilines, α-chloroacetyl chloride and 2'hydroxyacetophenones. 36 The reaction exhibited good functional group tolerance under the optimized conditions (Cs2CO3 as base, in dry DMF upon microwave irradiation at 140 °C) (Scheme 1). When electron-donating substituents were attached to 2'-hydroxyacetophenones, the yield of the corresponding product got reduced rapidly.…”
Section: Synthesis Of Benzofuran-2-carboxylic Acid Derivativesmentioning
confidence: 99%
“…Radi et al succeeded in achieving substituted benzofuran-2-carboxamides via microwave assisted multi-component reaction of anilines, α-chloroacetyl chloride and 2'hydroxyacetophenones. 36 The reaction exhibited good functional group tolerance under the optimized conditions (Cs2CO3 as base, in dry DMF upon microwave irradiation at 140 °C) (Scheme 1). When electron-donating substituents were attached to 2'-hydroxyacetophenones, the yield of the corresponding product got reduced rapidly.…”
Section: Synthesis Of Benzofuran-2-carboxylic Acid Derivativesmentioning
confidence: 99%
“…This step was followed by treating 3 with triphenylphosphine to give phosphonium salt (36) with dry benzene as solvent and refluxed for five hours. Reacting these salts with various benzoyl chloride (37) and methyl/formyl chloride (39) under reflux in toluene in attendance of triethylamine as base results in formation of title compounds represented in Scheme 3 and Scheme 4. [37] Qiu et al synthesized small molecule that is asymmetric named as R3T-TBFO (Scheme 5) based on thieno[2,3f]benzofuran.…”
Section: Synthetic Strategies Of Benzofuran Derivativesmentioning
confidence: 99%
“…A diversity oriented multicomponent protocol for the synthesis of benzofuran‐2‐carboxamides was established by Paolo et al . Several substituted furans such as 3‐aminobenzofurans, 3‐alkylbenzofurans, and 3‐unsubstituted benzofurans were synthesised from 2′‐hydroxyacetophenones, benzonitriles, aldehydes and readily available amines.…”
Section: Classificationmentioning
confidence: 99%