Synthesis of intermediate sitting-atop complexes (i-SAT) from the reaction between free base meso-tetraarylporphyrins and phosphorus(III) chloride in solvent free media

Polyhedron ◽  
2008 ◽  
Vol 27 (15) ◽  
pp. 3263-3266 ◽  
Author(s):  
Hossein Dehghani ◽  
Maryam Shaterian
Keyword(s):  
Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 164
Author(s):  
Patrícia M. Carvalho ◽  
Rita C. Guedes ◽  
Maria R. Bronze ◽  
Célia M. C. Faustino ◽  
Maria H. L. Ribeiro

Lipoaminoacids (LAA) are an important group of biosurfactants, formed by a polar hydrophilic part (amino acid) and a hydrophobic tail (lipid). The gemini LAA structures allow the formation of a supramolecular complex with bioactive molecules, like DNA, which provides them with good transfection efficiency. Since lipases are naturally involved in lipid and protein metabolism, they are an alternative to the chemical production of LAA, offering an eco-friendly biosynthetic process option. This work aimed to design the production of novel cystine derived gemini through a bioconversion system using immobilized lipases. Three lipases were used: porcine pancreatic lipase (PPL); lipase from Thermomyces lanuginosus (TLL); and lipase from Rizhomucor miehei (RML). PPL was immobilized in sol-gel lenses. L-cystine dihydrochloride and dodecylamine were used as substrates for the bioreaction. The production of LAA was evaluated by thin layer chromatography (TLC), and colorimetric reaction with eosin. The identification and quantification was carried out by High Performance Liquid Chromatographer-Mass Spectrometry (HPLC-MS/MS). The optimization of media design included co-solvent (methanol, dimethylsulfoxide), biphasic (n-hexane and 2-propanol) or solvent-free media, in order to improve the biocatalytic reaction rates and yields. Moreover, a new medium was tested where dodecylamine was melted and added to the cystine and to the biocatalyst, building a system of mainly undissolved substrates, leading to 5 mg/mL of LAA. Most of the volume turned into foam, which indicated the production of the biosurfactant. For the first time, the gemini derived cystine lipoaminoacid was produced, identified, and quantified in both co-solvent and solvent-free media, with the lipases PPL, RML, and TLL.


2018 ◽  
Vol 20 (7) ◽  
pp. 1491-1498 ◽  
Author(s):  
Liang Chang ◽  
Nadja Klipfel ◽  
Luc Dechoux ◽  
Serge Thorimbert

An efficient and sustainable method to prepare pharmaceutically important trifluoromethyl-benzenes from bio-based methyl coumalate in high yields, in a solvent-free tBuOK-catalyzed domino sequence.


Synlett ◽  
2004 ◽  
Vol 2004 (11) ◽  
pp. 1980-1984 ◽  
Author(s):  
Mohammad Khodaei ◽  
Ahmad Khosropour ◽  
Mehdi Kookhazadeh

2011 ◽  
Vol 102 (20) ◽  
pp. 9653-9658 ◽  
Author(s):  
Ilvania C. Véras ◽  
Frederico A.L. Silva ◽  
Astria D. Ferrão-Gonzales ◽  
Vitor Hugo Moreau

2014 ◽  
Vol 79 (8) ◽  
pp. 921-926 ◽  
Author(s):  
Omid Marvi ◽  
Masoud Giahi ◽  
Pouran Ayub ◽  
Mohammad Nikpasand

A series of ?-amino-?, ?-unsaturated ketones and esters synthesized from the reaction of different amines with 1,3- dicarbonyl compounds in solvent-free media using montmorillonite K-10 clay as solid recyclable heterogeneous acidic catalyst and microwave irradiation in good to excellent yields.


2019 ◽  
Vol 48 (31) ◽  
pp. 11978-11984 ◽  
Author(s):  
Suman Das ◽  
Himadri Karmakar ◽  
Jayeeta Bhattacharjee ◽  
Tarun K. Panda

Catalytic chemo-selective reduction of tert-amides with pinacolborane (HBpin) to furnish the corresponding tert-amines using an Earth-abundant Al complex under solvent-free, base-free and mild conditions is reported.


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