<i>ortho</i> -Nb <sub>2</sub> O <sub>5</sub> as a recyclable heterogeneous catalyst for the synthesis of 2-substituted benzimidazoles and quinazolinones in an aqueous medium <i>via</i> oxidative dehydrogenative coupling

Niobium pentoxide with a deformed orthorhombic phase (<i>ortho</i>-Nb<sub>2</sub>O<sub>5</sub>) was found to be an efficient heterogeneous catalyst for the synthesis of N-heterocyclic compounds such as 2-substituted benzimidazoles and quinazolinones from primary alcohols <i>via</i> oxidative dehydrogenative coupling in an aqueous medium. This environmentally benign method uses a bench-stable, heterogeneous, and biologically inert niobium metal-based catalyst, and the catalytic system is free of toxic metals, additives, oxidants, solvents, and byproducts. The catalyst is compatible with different substrates, and the desired benzimidazoles and quinazolinones were obtained in moderate to good yields. It is recyclable and can be used five times without significant loss in activity.

Authors

Institutions

Publication Details

Journal
Dalton Transactions
Published
2025-01-01
DOI
https://doi.org/10.1039/d5dt00353a
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

ortho -Nb 2 O 5 as a recyclable heterogeneous catalyst for the synthesis of 2-substituted benzimidazoles and quinazolinones in an aqueous medium via oxidative dehydrogenative coupling

Rajasekharan Jayakumari Deepak, Ramasamy Karvembu, Thiagu Pavin
Dalton Transactions
Quinazolinone synthesis and applications
article

ortho -Nb 2 O 5 as a recyclable heterogeneous catalyst for the synthesis of 2-substituted benzimidazoles and quinazolinones in an aqueous medium via oxidative dehydrogenative coupling

Rajasekharan Jayakumari Deepak, Ramasamy Karvembu, Thiagu Pavin
article en

Abstract

Niobium pentoxide with a deformed orthorhombic phase (<i>ortho</i>-Nb<sub>2</sub>O<sub>5</sub>) was found to be an efficient heterogeneous catalyst for the synthesis of N-heterocyclic compounds such as 2-substituted benzimidazoles and quinazolinones from primary alcohols <i>via</i> oxidative dehydrogenative coupling in an aqueous medium. This environmentally benign method uses a bench-stable, heterogeneous, and biologically inert niobium metal-based catalyst, and the catalytic system is free of toxic metals, additives, oxidants, solvents, and byproducts. The catalyst is compatible with different substrates, and the desired benzimidazoles and quinazolinones were obtained in moderate to good yields. It is recyclable and can be used five times without significant loss in activity.

Dalton TransactionsVol. 54(26)
National Institute of Technology Tiruchirappalli (IN)
Openalex Percentile: Top 91%
Quinazolinone synthesis and applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.