A green and efficient method for the synthesis of pyrroles using a deep eutectic solvent ([CholineCl][ZnCl2]3) under solvent-free sonication
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A green and efficient method for the synthesis of pyrroles using a deep eutectic solvent ([CholineCl][ZnCl2]3) under solvent-free sonication
Authors
Keywords
-
Journal
NEW JOURNAL OF CHEMISTRY
Volume 41, Issue 21, Pages 12481-12489
Publisher
Royal Society of Chemistry (RSC)
Online
2017-09-12
DOI
10.1039/c7nj02396k
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Physicochemical properties of deep eutectic solvents formed by choline chloride and phenolic compounds at T = (293.15 to 333.15) K: The influence of electronic effect of substitution group
- (2017) Jiahong Zhu et al. JOURNAL OF MOLECULAR LIQUIDS
- Hydrogen Bond Donor/Acceptor Cosolvent-Modified Choline Chloride-Based Deep Eutectic Solvents
- (2017) Ashish Pandey et al. JOURNAL OF PHYSICAL CHEMISTRY B
- Exploiting Deep Eutectic Solvents and Organolithium Reagent Partnerships: Chemoselective Ultrafast Addition to Imines and Quinolines Under Aerobic Ambient Temperature Conditions
- (2016) Cristian Vidal et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Acidic Ionic Liquids
- (2016) Ananda S. Amarasekara CHEMICAL REVIEWS
- Ruthenium Metal-Organic Frameworks with Different Defect Types: Influence on Porosity, Sorption, and Catalytic Properties
- (2016) Wenhua Zhang et al. CHEMISTRY-A EUROPEAN JOURNAL
- Deep Eutectic Solvents: The Organic Reaction Medium of the Century
- (2016) Diego A. Alonso et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Nitropyrrole natural products: isolation, biosynthesis and total synthesis
- (2016) Xiao-Bo Ding et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Total Synthesis of the Proposed Structure of Marineosin A
- (2016) Bing Xu et al. ORGANIC LETTERS
- Direct Synthesis of Pyrroles via Heterogeneous Catalytic Condensation of Anilines with Bioderived Furans
- (2016) Lei Tao et al. ACS Catalysis
- Convenient synthesis of substituted pyrroles via a cerium (IV) ammonium nitrate (CAN)-catalyzed Paal–Knorr reaction
- (2016) Ahmed Kamal et al. Arabian Journal of Chemistry
- Deep eutectic solvent choline chloride·2CrCl3·6H2O: an efficient catalyst for esterification of formic and acetic acid at room temperature
- (2016) Jin Cao et al. RSC Advances
- Deep Eutectic Mixtures: Promising Sustainable Solvents for Metal-Catalysed and Metal-Mediated Organic Reactions
- (2015) Joaquín García-Álvarez EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
- Greener Paal-Knorr Pyrrole Synthesis by Mechanical Activation
- (2015) Liudvikas Akelis et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- A concise synthesis of (+)-batzelladine B from simple pyrrole-based starting materials
- (2015) Brendan T. Parr et al. NATURE
- Mechanism of the Paal–Knorr reaction: the importance of water mediated hemialcohol pathway
- (2015) Sheenu Abbat et al. RSC Advances
- Acid- and metal-free synthesis of annulated pyrroles in a deep eutectic solvent
- (2015) Sunil M. Rokade et al. RSC Advances
- Introducing Deep Eutectic Solvents to Polar Organometallic Chemistry: Chemoselective Addition of Organolithium and Grignard Reagents to Ketones in Air
- (2014) Cristian Vidal et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Deep Eutectic Solvents (DESs) and Their Applications
- (2014) Emma L. Smith et al. CHEMICAL REVIEWS
- Access to Pyrrole Derivatives in Water with the Assistance of Methylated Cyclodextrins
- (2014) Stéphane Menuel et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- l-(+)-Tartaric acid and choline chloride based deep eutectic solvent: An efficient and reusable medium for synthesis of N-substituted pyrroles via Clauson-Kaas reaction
- (2014) Ping Wang et al. JOURNAL OF MOLECULAR LIQUIDS
- Low-Transition-Temperature Mixtures (LTTMs): A New Generation of Designer Solvents
- (2013) María Francisco et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Halometallate ionic liquids – revisited
- (2013) J. Estager et al. CHEMICAL SOCIETY REVIEWS
- Glycerol based solvents: synthesis, properties and applications
- (2013) José I. García et al. GREEN CHEMISTRY
- Green and Rapid Strategy for Synthesis of Novel and Known Pyrroles by the Use of Molybdate Sulfuric Acid
- (2013) Bahador Karami et al. JOURNAL OF THE CHINESE CHEMICAL SOCIETY
- A sustainable catalytic pyrrole synthesis
- (2013) Stefan Michlik et al. Nature Chemistry
- Organic synthesis in deep eutectic solvents: Paal–Knorr reactions
- (2013) Scott Handy et al. TETRAHEDRON LETTERS
- Deep-eutectic solvents playing multiple roles in the synthesis of polymers and related materials
- (2012) Daniel Carriazo et al. CHEMICAL SOCIETY REVIEWS
- Deep eutectic solvents: syntheses, properties and applications
- (2012) Qinghua Zhang et al. CHEMICAL SOCIETY REVIEWS
- Room temperature aqueous Paal–Knorr pyrrole synthesis catalyzed by aluminum tris(dodecyl sulfate)trihydrate
- (2012) Abbas Ali Jafari et al. Environmental Chemistry Letters
- Low melting mixtures in organic synthesis – an alternative to ionic liquids?
- (2012) Carolin Ruß et al. GREEN CHEMISTRY
- Paal–Knorr reaction catalyzed by metal–organic framework IRMOF-3 as an efficient and reusable heterogeneous catalyst
- (2012) Nam T.S. Phan et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- Silica-supported bismuth(III) chloride as a new recyclable heterogeneous catalyst for the Paal–Knorr pyrrole synthesis
- (2012) Kioumars Aghapoor et al. JOURNAL OF ORGANOMETALLIC CHEMISTRY
- Polystyrene-supported GaCl3 as a highly efficient and recyclable heterogeneous Lewis acid catalyst for one-pot synthesis of N-substituted pyrroles
- (2012) Ali Rahmatpour JOURNAL OF ORGANOMETALLIC CHEMISTRY
- Flow synthesis using gaseous ammonia in a Teflon AF-2400 tube-in-tube reactor: Paal–Knorr pyrrole formation and gas concentration measurement by inline flow titration
- (2012) Philippa B. Cranwell et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- ZrOCl2·8H2O as a highly efficient, eco-friendly and recyclable Lewis acid catalyst for one-pot synthesis of N-substituted pyrroles under solvent-free conditions at room temperature
- (2011) Ali Rahmatpour APPLIED ORGANOMETALLIC CHEMISTRY
- Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis. 2
- (2011) Jason P. Hallett et al. CHEMICAL REVIEWS
- Silica-supported antimony(III) chloride as a mild and reusable catalyst for the Paal–Knorr pyrrole synthesis
- (2011) Hossein Reza Darabi et al. Environmental Chemistry Letters
- Validation of Speciation Techniques: A Study of Chlorozincate(II) Ionic Liquids
- (2011) Julien Estager et al. INORGANIC CHEMISTRY
- Synthesis of Unsymmetrical 3,4-Diaryl-3-pyrrolin-2-ones Utilizing Pyrrole Weinreb Amides
- (2011) Jessica G. Greger et al. JOURNAL OF ORGANIC CHEMISTRY
- Glycerol eutectics as sustainable solvent systems
- (2010) Andrew P. Abbott et al. GREEN CHEMISTRY
- Access to 2,5-Diamidopyrroles and 2,5-Diamidofurans by Au(I)-Catalyzed Double Hydroamination or Hydration of 1,3-Diynes
- (2010) Søren Kramer et al. ORGANIC LETTERS
- Silica sulfuric acid (SSA) as a solid acid heterogeneous catalyst for one-pot synthesis of substituted pyrroles under solvent-free conditions at room temperature
- (2010) Hojat Veisi TETRAHEDRON LETTERS
- Structural Analysis of [ChCl]m[ZnCl2]nIonic Liquid by X-ray Absorption Fine Structure Spectroscopy
- (2009) Yang Zou et al. JOURNAL OF PHYSICAL CHEMISTRY B
- Raman spectroscopy of ionic liquids derived from 1-n-butyl-3-methylimidazolium chloride and niobium chloride or zinc chloride mixtures
- (2008) Melquizedeque B. Alves et al. JOURNAL OF RAMAN SPECTROSCOPY
- Ultrasound-assisted synthesis of pyrroles catalyzed by zirconium chloride under solvent-free conditions
- (2008) Zhan-Hui Zhang et al. ULTRASONICS SONOCHEMISTRY
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started