Expeditious and selective synthesis of 2,4,5-trialkyl-1H-imdazoles and benzimidazoles via multicomponent one-pot reaction catalyzed by Schiff base dioxomolybdenum(VI) complex DOI
Jiaxin Zhang,

Miao Wang,

Junli Zhang

et al.

Journal of Organometallic Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 123420 - 123420

Published: Oct. 1, 2024

Language: Английский

Recent progress in the synthesis of imidazoquinoline derivatives DOI Creative Commons

Warda Jahangir,

Sumayya Akram,

Sana Aslam

et al.

Results in Chemistry, Journal Year: 2025, Volume and Issue: unknown, P. 102270 - 102270

Published: April 1, 2025

Language: Английский

Citations

0

Molybdenum‐Catalyzed Direct Synthesis of Pyrroles from Nitroarenes with Glycols as Reductants DOI Creative Commons
Sara Gómez‐Gil, Samuel Suárez‐Pantiga, M.R. Pedrosa

et al.

Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 21, 2024

Abstract A molybdenum‐catalyzed synthesis of N ‐(hetero)aryl pyrroles directly from inexpensive and commonly available (hetero)nitroarenes via reduction with pinacol annulation 1,4‐dicarbonyls or cyclobutane‐1,2‐diols has been described. The process does not require an inert atmosphere tolerates the presence air water. This non‐noble catalytic system shows high chemoselectivity, allowing a diverse range potentially reducible functional groups such as alkynes, alkenes, halogens, cyano, carbonyls. Moreover, this strategy enables reuse waste byproduct reactant, facilitating formation challenging accessible used reducing agents.

Language: Английский

Citations

1

Advancing quinoxaline chemistry: Sustainable and green synthesis using L-arabinose as a catalyst DOI

Sandip J. Detke,

Anuja D. Karwande,

Sai Srinivas Ponugoti

et al.

Synthetic Communications, Journal Year: 2024, Volume and Issue: 54(23), P. 2024 - 2037

Published: Oct. 24, 2024

In the present study, an innovative and eco-friendly methodology for synthesizing quinoxaline derivatives has been introduced, leveraging L-arabinose as a novel catalyst. This approach not only underscores feasibility of green chemistry in high-purity but also highlights enhanced sustainability process. Detailed mechanistic investigations revealed synergistic interactions between reactants, providing deeper understanding catalytic The synthesized compounds, due to their unique structural electronic properties, may find promising applications life material sciences such optoelectronics. Furthermore, our environmental impact assessment demonstrated significant reduction generated waste, solvent use, overall carbon footprint, aligning with global agenda sustainable development. research marks step forward chemistry, promoting adoption synthesis pathways while reinforcing principles environment-friendly chemical practices.

Language: Английский

Citations

0

Expeditious and selective synthesis of 2,4,5-trialkyl-1H-imdazoles and benzimidazoles via multicomponent one-pot reaction catalyzed by Schiff base dioxomolybdenum(VI) complex DOI
Jiaxin Zhang,

Miao Wang,

Junli Zhang

et al.

Journal of Organometallic Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 123420 - 123420

Published: Oct. 1, 2024

Language: Английский

Citations

0