Green solvent ionic liquids: structural directing pioneers for microwave-assisted synthesis of controlled MgO nanostructures

RSC Advances ◽  
2016 ◽  
Vol 6 (38) ◽  
pp. 31675-31686 ◽  
Author(s):  
Arvind H. Jadhav ◽  
Alan C. Lim ◽  
Gaurav M. Thorat ◽  
Harsharaj S. Jadhav ◽  
Jeong Gil Seo
Keyword(s):  
Ionic Liquids ◽  
Microwave Assisted Synthesis ◽  
Green Solvent ◽  
One Pot ◽  
Microwave Assisted

Various MgO nanostructures were obtained via one-pot microwave-assisted synthesis in various structural directing ionic liquids.

Microwave-assisted synthesis in water: first one-pot synthesis of a novel class of polysubstituted benzo[4,5]imidazo[1,2-b]pyridazines via intramolecular SNAr

RSC Advances ◽  
2015 ◽  
Vol 5 (108) ◽  
pp. 89226-89237 ◽  
Author(s):  
Haider Behbehani ◽  
Hamada Mohamed Ibrahim
Keyword(s):  
Energy Source ◽  
Green Energy ◽  
Microwave Assisted Synthesis ◽  
Green Solvent ◽  
One Pot ◽  
Microwave Assisted ◽  
One Pot Synthesis ◽  
Synthesis Protocol

A novel and straightforward one-pot synthesis protocol has been developed for the synthesis of benzo[4,5]imidazo[1,2-b]pyridazines through intramolecular SNAr, utilizing water as a green solvent and microwaves as an efficient green energy source.

scholarly journals Reaction of o-Aminobenzamides with Dialkyl Carbonates and Ionic Liquids: A Novel one-pot, High-yield, Microwave-assisted Synthesis of 1-Alkylquinazoline-2,4-diones

2017 ◽  
Vol 56 (2) ◽  
Author(s):  
Leticia Guerrero R. ◽  
Ignacio A. Rivero
Keyword(s):  
Ionic Liquids ◽  
Alkylating Agents ◽  
High Yield ◽  
Microwave Assisted Synthesis ◽  
The Novel ◽  
Library Synthesis ◽  
One Pot ◽  
Microwave Assisted ◽  
Dialkyl Carbonates ◽  
Alkylation Reactions

A simple and efficient methodology for the synthesis of 1-alkyl-2,4-(1<em>H</em>,3<em>H</em>)-quinazolinediones from <em>o</em>-aminobenzamides has been developed. The novel one-pot cyclization-alkylation reactions are easier and faster than any other reported protocols and resulted in excellent yields (96-98%) and high purities, making this methodology suitable for library synthesis in drug discovery efforts. By applying microwave irradiation at 130 °C and in the presence of ionic liquids, dimethyl or diethyl carbonates simultaneously act as carbonylating and alkylating agents.

scholarly journals One-Pot Microwave-Assisted Synthesis of Water-Soluble Pyran-2,4,5-triol Glucose Amine Schiff Base Derivative: XRD/HSA Interactions, Crystal Structure, Spectral, Thermal and a DFT/TD-DFT

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 117
Author(s):  
Yousef Hijji ◽  
Rajeesha Rajan ◽  
Hamdi Ben Yahia ◽  
Said Mansour ◽  
Abdelkader Zarrouk ◽  
...  
Keyword(s):  
Schiff Base ◽  
Molecular Orbital ◽  
Density Functional ◽  
Condensation Reaction ◽  
3D Structure ◽  
Water Soluble ◽  
Microwave Assisted Synthesis ◽  
One Pot ◽  
Microwave Assisted ◽  
Td Dft

The(3R,4R,6R)-3-(((E)-2-hydroxybenzylidene)amino)-6-(hydroxymethyl)tetrahydro-2H-pyran-2,4,5-triol water-soluble Glucose amine Schiff base (GASB-1) product was made available by condensation of 2-hydroxybenzaldehyde with (3R,6R)-3-amino-6-(hydroxymethyl)-tetra-hydro-2H-pyran-2,4,5-triol under mono-mode microwave heating. A one-pot 5-minute microwave-assisted reaction was required to complete the condensation reaction with 90% yield and without having byproducts. The 3D structure of GASB-1 was solved from single crystal X-ray diffraction data and computed by DFT/6-311G(d,p). The Hirshfeld surface analysis (HSA), molecular electronic potential (MEP), Mulliken atomic charge (MAC), and natural population analysis (NPA) were performed. The IR and UV-Vis spectra were matched to their density functional theory (DFT) relatives and the thermal behavior was resolved in an open-room condition via thermogravimetry/Derivative thermogravimetry (TG/DTG) and differential scanning calorimetry (DSC). The highest occupied molecular orbital/lowest unoccupied molecular orbital (HOMO/LUMO), density of state (DOS), and time-dependence TD-DFT computations were correlated to the experimental electron transfer in water and acrylonitrile solvents.

Microwave-assisted synthesis of 1-aryl-1H-indazoles via one-pot two-step Cu-catalyzed intramolecular N-arylation of arylhydrazones

2005 ◽  
Vol 46 (44) ◽  
pp. 7553-7557 ◽  
Author(s):  
Chittari Pabba ◽  
Hong-Jun Wang ◽  
Susan R. Mulligan ◽  
Zhen-Jia Chen ◽  
Todd M. Stark ◽  
...  
Keyword(s):  
Microwave Assisted Synthesis ◽  
One Pot ◽  
Microwave Assisted

Facile one-pot microwave-assisted synthesis of tungsten-doped BiVO4/WO3 heterojunctions with enhanced photocatalytic activity

2020 ◽  
Vol 125 ◽  
pp. 110783 ◽  
Author(s):  
Caroline H. Claudino ◽  
Maria Kuznetsova ◽  
Bárbara S. Rodrigues ◽  
Changqiang Chen ◽  
Zhiyu Wang ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Microwave Assisted Synthesis ◽  
One Pot ◽  
Microwave Assisted

scholarly journals Screening of Natural Deep Eutectic Solvents for Green Synthesis of 2-methyl-3-substituted Quinazolinones and Microwave-Assisted Synthesis of 3-aryl Quinazolinones in Ethanol

2020 ◽  
Vol 92 (4) ◽  
pp. 511-517
Author(s):  
Mario Komar ◽  
Maja Molnar ◽  
Anastazija Konjarević
Keyword(s):  
Green Synthesis ◽  
Anthranilic Acid ◽  
Deep Eutectic Solvents ◽  
13C Nmr Spectroscopy ◽  
Microwave Assisted Synthesis ◽  
One Pot ◽  
1H And 13C Nmr ◽  
Microwave Assisted ◽  
Natural Deep Eutectic Solvents ◽  
Quinazolinone Derivatives

In this study, two fast and efficient protocols for green synthesis of 3-substituted quinazolinones were perfomed. A synthesis of 2-methyl-3-substituted quinazolinones was performed in natural deep eutectic solvents, while 3-aryl quinazolinones were obtained by using microwave assisted synthesis. Benzoxazinone, which was used as an intermediate in the synthesis of 2-methyl-3-substituted quinazolinones, was prepared conventionally from anthranilic acid and acetic anhydride. In order to find the most appropriate synthetic path, twenty natural deep eutectic solvents were applied as a solvent in these syntheses. Choline chloride:urea (1 : 2) was found to be the most efficient solvent and was further used in the synthesis of 2-methyl quinazolinone derivatives (2–12). 3-Aryl quinazolinones (13–17), on the other hand, were synthesized in one-pot microwave-assisted reaction of anthranilic acid, different amines and trimethyl orthoformate. All compounds were synthesized in good to excellent yields, characterized by LC-MS/MS spectrometry and 1H- and 13C-NMR spectroscopy.

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