A pseudo six-component process for the synthesis of tetrahydrodipyrazolo pyridines using an ionic liquid immobilized on a FeNi3 nanocatalyst
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A pseudo six-component process for the synthesis of tetrahydrodipyrazolo pyridines using an ionic liquid immobilized on a FeNi3 nanocatalyst
Authors
Keywords
-
Journal
RSC Advances
Volume 6, Issue 40, Pages 33676-33685
Publisher
Royal Society of Chemistry (RSC)
Online
2016-03-31
DOI
10.1039/c6ra02906j
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Facile and efficient synthesis of pyrazoloisoquinoline and pyrazolopyridine derivatives using recoverable carbonaceous material as solid acid catalyst
- (2015) Zhu Chen et al. TETRAHEDRON LETTERS
- Three-component synthesis of cyclic $\beta $-aminoesters using CeO$_{2}$ nanoparticles as an efficient and reusable catalyst
- (2015) Javad SAFAEI-GHOMI et al. TURKISH JOURNAL OF CHEMISTRY
- Ultrasonic-accelerated rapid protocol for the improved synthesis of pyrazoles
- (2015) Nhlanhla Gracious Shabalala et al. ULTRASONICS SONOCHEMISTRY
- Facile, novel and efficient synthesis of new pyrazolo[3,4-b]pyridine products from condensation of pyrazole-5-amine derivatives and activated carbonyl groups
- (2015) A. Ghaedi et al. RSC Advances
- A heteropolyacid-based ionic liquid immobilized onto Fe3O4/SiO2/salen/Mn as an environmentally friendly catalyst in a multi-component reaction
- (2015) Seyed Mohsen Sadeghzadeh RSC Advances
- Ionic liquid immobilized on FeNi3 as catalysts for efficient, green, and one-pot synthesis of 1,3-thiazolidin-4-one
- (2014) Seyed Mohsen Sadeghzadeh et al. JOURNAL OF MOLECULAR LIQUIDS
- Nano-magnetite (Fe3O4) as a support for recyclable catalysts in the development of sustainable methodologies
- (2013) Manoj B. Gawande et al. CHEMICAL SOCIETY REVIEWS
- Magnetic nanoparticle supported hyperbranched polyglycerol catalysts for synthesis of 4H-benzo[b]pyran
- (2013) Mohammad Ali Nasseri et al. MONATSHEFTE FUR CHEMIE
- l-Proline-catalyzed three-component domino reactions for the synthesis of highly functionalized pyrazolo[3,4-b]pyridines
- (2013) Pethaiah Gunasekaran et al. TETRAHEDRON LETTERS
- Quinuclidine Stabilized on FeNi3Nanoparticles as Catalysts for Efficient, Green, and One-Pot Synthesis of Triazolo[1,2-a]indazole-triones
- (2013) Seyed Mohsen Sadeghzadeh ChemPlusChem
- Immobilized functional ionic liquids: efficient, green, and reusable catalysts
- (2012) Hu Li et al. RSC Advances
- Pyrazolopyridine inhibitors of B-RafV600E. Part 3: An increase in aqueous solubility via the disruption of crystal packing
- (2011) Steve Wenglowsky et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Highly Potent 5-Aminotetrahydropyrazolopyridines: Enantioselective Dopamine D3Receptor Binding, Functional Selectivity, and Analysis of Receptor−Ligand Interactions
- (2011) Nuska Tschammer et al. JOURNAL OF MEDICINAL CHEMISTRY
- A facile protocol for the synthesis of 4-aryl-1,4,7,8-tetrahydro-3,5-dimethyldipyrazolo[3,4-b:4′,3′-e]pyridine derivatives by a Hantzsch-type reaction
- (2011) Kun Zhao et al. MONATSHEFTE FUR CHEMIE
- Pyrazolopyridines as potent PDE4B inhibitors: 5-Heterocycle SAR
- (2010) Charlotte J. Mitchell et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Multicomponent reactions for the synthesis of pyrroles
- (2010) Verónica Estévez et al. CHEMICAL SOCIETY REVIEWS
- Synthesis and biological evaluation of 3,6-diamino-1H-pyrazolo[3,4-b]pyridine derivatives as protein kinase inhibitors
- (2009) Mourad Chioua et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Pyrazolopyridines with potent activity against herpesviruses: Effects of C5 substituents on antiviral activity
- (2007) Kristjan S. Gudmundsson et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk 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