An expeditious green route toward 2-aryl-4-phenyl-1H-imidazoles
Open Access
- 20 September 2014
- journal article
- Published by Springer Science and Business Media LLC in BMC Chemistry
- Vol. 4 (1), 9
- https://doi.org/10.1186/s13588-014-0009-7
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- An Effective Microwave-Induced Iodine-Catalyzed Method for the Synthesis of Quinoxalines via Condensation of 1,2-Diamines with 1,2-Dicarbonyl CompoundsMolecules, 2010
- An Expeditious Synthesis of N-substituted Pyrroles via Microwave-Induced Iodine-Catalyzed Reactions under Solventless ConditionsMolecules, 2010
- Microwave‐Induced Stereocontrol of β‐Lactam Formation with an N‐Benzylidene‐9,10‐dihydrophenanthren‐3‐amine via Staudinger CycloadditionHelvetica Chimica Acta, 2010
- Facile synthesis of N-substituted pyrroles via microwave-induced bismuth nitrate-catalyzed reactionTetrahedron Letters, 2009
- Ultrasound assisted reactions of steroid analogous of anticipated biological activitiesUltrasonics Sonochemistry, 2009
- Aqueous microwave chemistry: a clean and green synthetic tool for rapid drug discoveryChemical Society Reviews, 2008
- A mild and efficient ultrasound-assisted synthesis of diaryl ethers without any catalystUltrasonics Sonochemistry, 2007
- A Practical Synthesis of 2,4(5)-Diarylimidazoles from Simple Building BlocksThe Journal of Organic Chemistry, 2007
- Eco-friendly synthesis of imines by ultrasound irradiationTetrahedron Letters, 2007
- Solvent-Free Organic SynthesisChemical Reviews, 2000