Cascade covalent and coordination bond formation for Ti-based cage assembly: catalysis and coordination bifunctionality of TiCl4

2018 ◽  
Vol 47 (10) ◽  
pp. 3239-3242 ◽  
Author(s):  
Jing Tong ◽  
Tingting Xu ◽  
Shengjun Liu ◽  
Junxiang Zhang ◽  
Xudong Hou ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Lewis Acid ◽  
Bond Formation ◽  
Acid Catalyst ◽  
Coordination Bond ◽  
Solvothermal Reaction ◽  
Aminobenzoic Acid ◽  
One Pot ◽  
Coordination Sites ◽  
Lewis Acid Catalyst

Ti-based cage of [Ti4O2L4Cl8] (L = 4-acetamidobenzoic acid) is synthesized by a one-pot solvothermal reaction of the 4-aminobenzoic acid, acetic acid and TiCl4. Ti(iv) ion functions as a Lewis acid catalyst and coordination sites to afford Ti-based cage formation in a cascade fashion.

ZrOCl2·8H2O: an efficient Lewis acid catalyst for the one-pot multicomponent synthesis of β-acetamido ketones

Tetrahedron ◽  
2006 ◽  
Vol 62 (17) ◽  
pp. 4059-4064 ◽  
Author(s):  
Rina Ghosh ◽  
Swarupananda Maiti ◽  
Arijit Chakraborty ◽  
Santu Chakraborty ◽  
Alok K. Mukherjee
Keyword(s):  
Lewis Acid ◽  
Acid Catalyst ◽  
Multicomponent Synthesis ◽  
One Pot ◽  
Lewis Acid Catalyst ◽  
The One

Lewis Acid Promoted, One-Pot Synthesis of Fluoroquinolone Clubbed 1,3,4-Thiadiazole Motifs under Microwave Irradiation: Their Biological Activities

2020 ◽  
Vol 7 (1) ◽  
pp. 60-66
Author(s):  
Navin B. Patel ◽  
Rahul B. Parmar ◽  
Hetal I. Soni
Keyword(s):  
Reaction Time ◽  
Microwave Irradiation ◽  
Lewis Acid ◽  
Acid Catalyst ◽  
Antitubercular Activity ◽  
Biologically Active ◽  
High Yield ◽  
One Pot ◽  
One Pot Synthesis ◽  
Lewis Acid Catalyst

Background: A Lewis acid promoted efficient and facile procedure for one-pot synthesis of a novel series of fluoroquinolone clubbed with thiadiazoles motifs under microwave irradiation is described here. This technique has more advantages such as high yield, a clean procedure, low reaction time, simple work-up and use of Lewis acid catalyst. Objective: Our aim is to generate a biologically active 1,3,4- thiadiazole ring system by using a onepot synthesis method and microwave-assisted heating. High yield and low reaction time were the main purposes to synthesize bioactive fluoroquinolone clubbed 1,3,4- thiadiazole moiety. Methods: Fluoroquinolone Clubbed 1,3,4-Thiadiazole Motifs was prepared by Lewis acid promoted, one-pot synthesis, under microwave irradiation. All the synthesized molecules were determined by IR, 1H NMR, 13C NMR, and Mass spectra. The antimicrobial activity of synthesized compounds was examined against two Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa), two Gram-positive bacteria (Staphylococcus aureus, Streptococcus pyogenes), and three fungi (Candida albicans, Aspergillus niger, Aspergillus clavatus) using the MIC (Minimal Inhibitory Concentration) method and antitubercular activity H37Rv using L. J. Slope Method. Results: Lewis acid promoted, one-pot synthesis of Fluoroquinolone clubbed 1,3,4-Thiadiazole motifs under microwave irradiation is an extremely beneficial method because of its low reaction time and good yield. Some of these novel derivatives showed moderate to good in vitro antibacterial, antifungal, and antitubercular activity. Conclusion: One-pot synthesis of 1,3,4-Thiadiazole by using Lewis acid catalyst gives a good result for saving time and also getting more production of novel heterocyclic compounds with good antimicrobial properties via microwave heating method.

Antimony(III) chloride impregnated on alumina — An efficient and economical Lewis acid catalyst for one-pot synthesis of dihydropyrimidinones under solvent-free conditions

2006 ◽  
Vol 84 (3) ◽  
pp. 433-437 ◽  
Author(s):  
Kamal K Kapoor ◽  
Bilal A Ganai ◽  
Satish Kumar ◽  
Charanjeet S Andotra
Keyword(s):  
Lewis Acid ◽  
Condensation Reaction ◽  
Thermal Conditions ◽  
Acid Catalyst ◽  
Solvent Free ◽  
One Pot ◽  
One Pot Synthesis ◽  
Solvent Free Conditions ◽  
Lewis Acid Catalyst

The antimony(III) chloride impregnated on alumina efficiently catalyses a one-pot, three-component condensation reaction among an aldehyde, a β-ketoester, and urea or thiourea to afford the corresponding dihydropyrimidinones in good to excellent yields. The reactions are probed in microwave (MW), ultrasonic, and thermal conditions and the best results are found using MW under solvent-free conditions.Key words: Biginelli dihydropyrimidinones synthesis, SbCl3–Al2O3, MW, sonication, solid supported.

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