Dual Utility of Heterogeneous Catalyst ZSM-5 for C-C Cleavage Leading to Nitriles, and for the Synthesis of Hydrazides
Author:
Affiliation:
1. Department of Pharmaceutical Sciences and Technology; Institution of Chemical Technology, Matunga (E); Mumbai 400 019 Maharashtra India
2. Department of Chemistry and Biochemistry; University of California; Santa Barbara CA 93106 USA
Funder
University Grand Commission
Publisher
Wiley
Subject
General Chemistry
Reference48 articles.
1. Lewis Acid-Catalyzed Denitrogenative Transannulation of Pyridotriazoles with Nitriles: Synthesis of Imidazopyridines
2. Copper-Catalyzed Synthesis of Substituted Benzothiazoles via Condensation of 2-Aminobenzenethiols with Nitriles
3. Pd-Catalyzed Aminocarbonylation of the Blaise Reaction Intermediate: One-Pot Synthesis of (Z)-3-Methyleneisoindolin-1-ones from Nitriles
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1. An efficient, green and solvent-free three-component synthesis of 2,4,6-triarylpyridines utilizing ZSM-5 as a heterogeneous catalyst;Synthetic Communications;2024-09-12
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3. Synthesis of Acyl Hydrazides from Carboxamides and Hydrazine Hydrate Under Metal‐Free Conditions at Room Temperature;Asian Journal of Organic Chemistry;2023-04-25
4. Synthesis of Aryl Nitriles via Aerobic Oxidative Cleavage of Aryl C=C Bonds with (NH4)2CO3 as the Nitrogen Source;Synlett;2022-01-18
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