ChemInform Abstract: Synthesis of Aryl/Alkyl(2,2′-bis-3-methylindolyl)methanes and Aryl(3,3′-bis-indolyl)methanes Promoted by Secondary Amine Based Ionic Liquids and Microwave Irradiation.

ChemInform ◽  
2012 ◽  
Vol 43 (48) ◽  
pp. no-no
Author(s):  
Pranab J. Das ◽  
Jupitara Das
Keyword(s):  
Ionic Liquids ◽  
Microwave Irradiation ◽  
Secondary Amine

Facile, high-yielding preparation of pyrrolidinium, piperidinium, morpholinium and 2,3-dihydro-1H-isoindolinium salts and ionic liquids from secondary amines

RSC Advances ◽  
2014 ◽  
Vol 4 (44) ◽  
pp. 23327-23337 ◽  
Author(s):  
Antony J. Ward ◽  
Anthony F. Masters ◽  
Thomas Maschmeyer
Keyword(s):  
Ionic Liquids ◽  
Microwave Irradiation ◽  
Anion Exchange ◽  
Secondary Amine ◽  
Secondary Amines ◽  
High Yield ◽  
Yield And Purity

High yield and purity heterocyclic salts and ionic liquids can be obtained via the microwave irradiation of equimolar amounts of a secondary amine and an α,ω-dibromoalkane in water in the presence of K2CO3 followed by anion exchange.

Eco-Friendly Synthesis of Pyrazoline Derivatives

2017 ◽  
Vol 9 (04) ◽  
Author(s):  
Mahesh G. Kharatmol ◽  
Deepali Jagdale
Keyword(s):  
Ionic Liquids ◽  
Microwave Irradiation ◽  
Organic Synthesis ◽  
Ultrasonic Irradiation ◽  
Minimal Energy ◽  
Anticancer Activities ◽  
Conventional Methods

Pyrazoline class of compounds serve as better moieties for an array of treatments, they have antibacterial, antifungal, antiinflammatory, antipyretic, diuretic, cardiovascular activities. Apart from these they also have anticancer activities. So, pertaining to its importance, many attempts are made to synthesize pyrazolines. Since conventional methods of organic synthesis are energy and time consuming. There are elaborate pathways for green and eco-friendly synthesis of pyrazoline derivatives including microwave irradiation, ultrasonic irradiation, grinding and use of ionic liquids which assures the synthesis of the same within much lesser time and by use of minimal energy

ChemInform Abstract: Morita-Baylis-Hillman Reaction in Water/Ionic Liquids under Microwave Irradiation.

ChemInform ◽  
2008 ◽  
Vol 39 (45) ◽  
Author(s):  
Rodrigo O. M. A. de Souza ◽  
Andrea L. F. de Souza ◽  
Tatiana L. Fernandez ◽  
Aires C. Silva ◽  
Vera L. P. Pereira ◽  
...  
Keyword(s):  
Ionic Liquids ◽  
Microwave Irradiation ◽  
Reaction In Water

Ionic liquids plus microwave irradiation: a general methodology for the retro-functionalization of single-walled carbon nanotubes

Nanoscale ◽  
2018 ◽  
Vol 10 (33) ◽  
pp. 15782-15787 ◽  
Author(s):  
Myriam Barrejón ◽  
Zois Syrgiannis ◽  
Maurizio Prato
Keyword(s):  
Carbon Nanotubes ◽  
Ionic Liquids ◽  
Microwave Irradiation ◽  
Single Walled Carbon Nanotubes ◽  
Single Walled Carbon ◽  
General Methodology ◽  
Walled Carbon Nanotubes

Tunable functionalization of SWCNTs through the use of ionic liquids under microwave irradiation.

scholarly journals Synthesis of Medicinally Important Indole Derivatives: A Review

2021 ◽  
Vol 15 (1) ◽  
pp. 1-16
Author(s):  
Deeptanu Sarkar ◽  
Andleeb Amin ◽  
Tanzeela Qadir ◽  
Praveen K. Sharma
Keyword(s):  
Ionic Liquids ◽  
Microwave Irradiation ◽  
Functional Group ◽  
Solid Acid ◽  
Solid Acid Catalyst ◽  
Acid Catalyst ◽  
Indole Derivatives ◽  
Site Specific ◽  
Bioactive Natural Products ◽  
Solvent Free Conditions

Indoles constitute a widely occurring functional group in nature and are present in an extensive number of bioactive natural products and medicinally important compounds. As a result, exponential increases in the development of novel methods for the formation of indole core along with site-specific indoles have been established. Conventional methods for the synthesis of indoles are getting replaced with green methods involving ionic liquids, water as a solvent, solid acid catalyst, microwave irradiation and the use of nanoparticles under solvent-free conditions. In addition, there are immense applications of the substituted indoles in diverse fields.

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