A facile and one-pot aqueous phase transfer of oleylamine capped Au NP with aminophenylboronic acid used as transfer and targeting ligand

2021 ◽  
Vol 148 ◽  
pp. 109810
Author(s):  
Zehra Karaagac ◽  
Sadi Yusufbeyoglu ◽  
Nilay Ildiz ◽  
Hanen Sellami ◽  
Ismail Ocsoy
2020 ◽  
Vol 24 (4) ◽  
pp. 465-471 ◽  
Author(s):  
Zita Rádai ◽  
Réka Szabó ◽  
Áron Szigetvári ◽  
Nóra Zsuzsa Kiss ◽  
Zoltán Mucsi ◽  
...  

The phospha-Brook rearrangement of dialkyl 1-aryl-1-hydroxymethylphosphonates (HPs) to the corresponding benzyl phosphates (BPs) has been elaborated under solid-liquid phase transfer catalytic conditions. The best procedure involved the use of triethylbenzylammonium chloride as the catalyst and Cs2CO3 as the base in acetonitrile as the solvent at room temperature. The substrate dependence of the rearrangement has been studied, and the mechanism of the transformation under discussion was explored by quantum chemical calculations. The key intermediate is an oxaphosphirane. The one-pot version starting with the Pudovik reaction has also been developed. The conditions of this tandem transformation were the same, as those for the one-step HP→BP conversion.


2017 ◽  
Vol 3 (4) ◽  
pp. 360-365
Author(s):  
Bijoy P. Mathew ◽  
Neha Batra ◽  
Mahendra Nath

2019 ◽  
Vol 4 (30) ◽  
pp. 8822-8828
Author(s):  
Arturo González‐Hernández ◽  
Jacobo Rivera‐Segura ◽  
Pascal G. Lacroix ◽  
Victor Barba

1993 ◽  
Vol 48 (4) ◽  
pp. 457-460 ◽  
Author(s):  
Eckehard V. Dehmlow ◽  
Christof Bollmann

Phase transfer catalytic isopropylation or tert-butylation of cyclopentadiene yields 1-6 in efficient one-pot procedures. Powdered potassium hydroxide or solid sodium hydride are the prefered bases, Aliquat 336 or dibenzo-18-crown-6 are the PT catalysts.


RSC Advances ◽  
2014 ◽  
Vol 4 (9) ◽  
pp. 4515-4522 ◽  
Author(s):  
R. M. Patil ◽  
P. B. Shete ◽  
N. D. Thorat ◽  
S. V. Otari ◽  
K. C. Barick ◽  
...  

Materials ◽  
2019 ◽  
Vol 12 (3) ◽  
pp. 540 ◽  
Author(s):  
Črt Dragar ◽  
Tanja Potrč ◽  
Sebastjan Nemec ◽  
Robert Roškar ◽  
Stane Pajk ◽  
...  

The development of various magnetically-responsive nanostructures is of great importance in biomedicine. The controlled assembly of many small superparamagnetic nanocrystals into large multi-core clusters is needed for effective magnetic drug delivery. Here, we present a novel one-pot method for the preparation of multi-core clusters for drug delivery (i.e., magnetic nanocarriers). The method is based on hot homogenization of a hydrophobic phase containing a nonpolar surfactant into an aqueous phase, using ultrasonication. The solvent-free hydrophobic phase that contained tetradecan-1-ol, γ-Fe2O3 nanocrystals, orlistat, and surfactant was dispersed into a warm aqueous surfactant solution, with the formation of small droplets. Then, a pre-cooled aqueous phase was added for rapid cooling and the formation of solid magnetic nanocarriers. Two different nonpolar surfactants, polyethylene glycol dodecyl ether (B4) and our own N1,N1-dimethyl-N2-(tricosan-12-yl)ethane-1,2-diamine (SP11), were investigated for the preparation of MC-B4 and MC-SP11 magnetic nanocarriers, respectively. The nanocarriers formed were of spherical shape, with mean hydrodynamic sizes <160 nm, good colloidal stability, and high drug loading (7.65 wt.%). The MC-B4 nanocarriers showed prolonged drug release, while no drug release was seen for the MC-SP11 nanocarriers over the same time frame. Thus, the selection of a nonpolar surfactant for preparation of magnetic nanocarriers is crucial to enable drug release from nanocarrier.


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