Synthesis of 3‐Acyl‐1‐Indenones by Oxidative Cyclization of Symmetrical and Unsymmetrical Aryldiynes Using Palladium Nanoparticles (Pd‐BNP) as Reusable Nano Catalyst

Abstract An efficient, stable and reusable binaphthyl stabilized palladium nanoparticles (Pd‐BNP) catalyzed synthesis of 3‐acyl‐1‐indenone derivatives from oxidative cyclization of symmetrical and unsymmetrical aryldiynes using DMSO as a solvent as well as an oxidant has been established. The scope of the reaction has been studied with various aryldiynes having electron‐donating and electron‐withdrawing groups that afforded good yields. Pd‐BNP catalyst can be recovered and reused for up to four cycles without major changes in particle size and reactivity.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2024-10-12
DOI
https://doi.org/10.1002/ajoc.202400260
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of 3‐Acyl‐1‐Indenones by Oxidative Cyclization of Symmetrical and Unsymmetrical Aryldiynes Using Palladium Nanoparticles (Pd‐BNP) as Reusable Nano Catalyst

Govindasamy Sekar, Gollapalli Narasimha Rao, Krishnamoorthy Kathirvel
Asian Journal of Organic Chemistry
Catalytic Alkyne Reactions
article

Synthesis of 3‐Acyl‐1‐Indenones by Oxidative Cyclization of Symmetrical and Unsymmetrical Aryldiynes Using Palladium Nanoparticles (Pd‐BNP) as Reusable Nano Catalyst

Govindasamy Sekar, Gollapalli Narasimha Rao, Krishnamoorthy Kathirvel
article en

Abstract

Abstract An efficient, stable and reusable binaphthyl stabilized palladium nanoparticles (Pd‐BNP) catalyzed synthesis of 3‐acyl‐1‐indenone derivatives from oxidative cyclization of symmetrical and unsymmetrical aryldiynes using DMSO as a solvent as well as an oxidant has been established. The scope of the reaction has been studied with various aryldiynes having electron‐donating and electron‐withdrawing groups that afforded good yields. Pd‐BNP catalyst can be recovered and reused for up to four cycles without major changes in particle size and reactivity.

Asian Journal of Organic ChemistryVol. 14(1)
Indian Institute of Technology Madras (IN)
Indian Institute of Technology Madras
Openalex Percentile: Top 87%
Catalytic Alkyne Reactions
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