Poly(2‐oxazoline)s terminated with 2,2′‐imino diacetic acid form noncovalent polymer–enzyme conjugates that are highly active in organic solvents

2018 ◽  
Vol 116 (2) ◽  
pp. 272-282 ◽  
Author(s):  
Montasser Hijazi ◽  
Pia Spiekermann ◽  
Christian Krumm ◽  
Joerg C. Tiller
2016 ◽  
Vol 12 ◽  
pp. 1566-1572 ◽  
Author(s):  
Anne L Schöffler ◽  
Ata Makarem ◽  
Frank Rominger ◽  
Bernd F Straub

A dinuclear N-heterocyclic carbene (NHC) copper complex efficiently catalyzes azide–alkyne cycloaddition (CuAAC) “click” reactions. The ancillary ligand comprises two 4,5-dimethyl-1,3-thiazol-2-ylidene units and an ethylene linker. The three-step preparation of the complex from commercially available starting compounds is more straightforward and cost-efficient than that of the previously described 1,2,4-triazol-5-ylidene derivatives. Kinetic experiments revealed its high catalytic CuAAC activity in organic solvents at room temperature. The activity increases upon addition of acetic acid, particularly for more acidic alkyne substrates. The modular catalyst design renders possible the exchange of N-heterocyclic carbene, linker, sacrificial ligand, and counter ion.


2021 ◽  
Vol 9 (8) ◽  
pp. 1790
Author(s):  
Amanda Staudt ◽  
Henrik Terholsen ◽  
Jasmin Kaur ◽  
Henrik Müller ◽  
Simon P. Godehard ◽  
...  

Biocatalytic transesterification is commonly carried out employing lipases in anhydrous organic solvents since hydrolases usually prefer hydrolysis over acyl transfer in bulk water. However, some promiscuous acyltransferases can catalyze acylation in an aqueous solution. In this study, a rational design was performed to enhance the acyltransferase selectivity and substrate scope of the Pyrobaculum calidifontis VA1 esterase (PestE). PestE wild type and variants were applied for the acylation of monoterpene alcohols. The mutant PestE_I208A is selective for (–)-menthyl acetate (E-Value = 55). Highly active acyltransferases were designed, allowing for complete conversion of (–)-citronellol to citronellyl acetate. Additionally, carvacrol was acetylated but with lower conversions. To the best of our knowledge, this is the first example of the biocatalytic acylation of a phenolic alcohol in bulk water. In addition, a high citronellol conversion of 92% was achieved with the more environmentally friendly and inexpensive acyl donor ethyl acetate using PestE_N288F as a catalyst. PestE_N288F exhibits good acyl transfer activity in an aqueous medium and low hydrolysis activity at the same time. Thus, our study demonstrates an alternative synthetic strategy for acylation of compounds without organic solvents.


2012 ◽  
Vol 40 (1-3) ◽  
pp. 15-23 ◽  
Author(s):  
Mohamed Samir Mohy Eldin ◽  
Emad Ali Soliman ◽  
Ahmed Abdel Fattah Elzatahry ◽  
Mohamed Ramadan Elaassar ◽  
Marwa Farouk Elkady ◽  
...  

The Analyst ◽  
2015 ◽  
Vol 140 (9) ◽  
pp. 2964-2968 ◽  
Author(s):  
Alexandra S. Demiyanova ◽  
Ivan Yu. Sakharov

Using FeIII–TAML, highly active peroxidase mimic, the sensitive chemiluminescence assays for the determination of benzoyl peroxide and tert-butyl hydroperoxide in the presence of organic solvents were developed.


2015 ◽  
Vol 210 (3) ◽  
pp. 473-482 ◽  
Author(s):  
Christodoulos Kaoutzanis ◽  
Eric Davies ◽  
Stefan W. Leichtle ◽  
Kathleen B. Welch ◽  
Suzanne Winter ◽  
...  

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