scholarly journals Pseudo enantiomeric mixed S/P ligands derived from carbohydrates for the 1,4-addition of phenyl boronic acid to cyclohexenone

RSC Advances ◽  
2016 ◽  
Vol 6 (4) ◽  
pp. 3041-3047 ◽  
Author(s):  
V. Valdivia ◽  
N. Bilbao ◽  
J. F. Moya ◽  
C. Rosales-Barrios ◽  
A. Salvador ◽  
...  

Mixed S/P ligands 3 and 10, good catalyst precursors for the Rh(i)-catalysed 1,4-addition of phenylboronic acid to cyclohexenone behave as enantiomers even though both derived from d-sugars.

2020 ◽  
Vol 44 (16) ◽  
pp. 6222-6231
Author(s):  
Velu Sadhasivam ◽  
Muniyasamy Harikrishnan ◽  
Ganesan Elamathi ◽  
Rajendran Balasaravanan ◽  
Sepperumal Murugesan ◽  
...  

Here, we report the synthesis of highly nitrogen-rich covalent organic polymers as a solid heterogeneous catalyst for the oxidation of phenylboronic acid under atmospheric conditions in an aqueous medium to achieve very good yields up to 99%.


2019 ◽  
Author(s):  
Meifeng Wang ◽  
Gan Zhu ◽  
Yiqun Li ◽  
Liuqun Gu

Arylboronic acids were widely used as efficient catalysts in direct amide formation and other organic transformations. Surprisingly, reports on their use as catalysts in carbohydrates synthesis are very rare even though boron acid-diol complexation was extensively investigated in molecular recognition for saccharides and so on. Here we developed an efficient arylboronic acids catalyzed dimerization of glucosamines forming deoxyfructosazine which is important compound in pharmaceutical and food industries, against a commonly held belief that excess amount of phenyl boronic acid (or boric acid) is a must. A catalytic mechanism was also proposed and arylboronic acids instead of their boronates was identified as catalysts.


2014 ◽  
Vol 58 (2) ◽  
pp. 33-35 ◽  
Author(s):  
Yuichi Aikyo ◽  
Masamichi Oh-Ishi

Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1854 ◽  
Author(s):  
Kentaro Yoshida ◽  
Akane Yamaguchi ◽  
Hiroki Midorikawa ◽  
Toshio Kamijo ◽  
Tetsuya Ono ◽  
...  

Phenylboronic acid-bearing polyamidoamine dendrimer (PBA-PAMAM)/poly(vinyl alcohol) (PVA) multilayer films were prepared through the layer-by-layer (LbL) deposition of PBA-PAMAM solution and PVA solution. PBA-PAMAM/PVA films were constructed successfully through the formation of boronate ester bonds between the boronic acid moiety in PBA and 1,3-diol units in PVA. When the (PBA-PAMAM/PVA)5 films were immersed in rose bengal (RB) solution, RB was adsorbed onto the LbL films. The amount of RB adsorbed was higher in the LbL films immersed in acidic solution than in basic solution. The release of RB from the LbL films was also promoted in the basic solution, while it was suppressed in the acidic solution. The boronic acid ester is oxidized to phenol by hydrogen peroxide (H2O2) and the carbon-boron bond is cleaved, so that the (PBA-PAMAM/PVA)5 films can be decomposed by immersion in H2O2 solution. Therefore, when RB-adsorbed (PBA-PAMAM/PVA)5 films were immersed in H2O2 solution, the release of RB was moderately promoted when the solution was weakly acidic.


2014 ◽  
Vol 57 (20) ◽  
pp. 8378-8397 ◽  
Author(s):  
Dean Y. Maeda ◽  
Angela M. Peck ◽  
Aaron D. Schuler ◽  
Mark T. Quinn ◽  
Liliya N. Kirpotina ◽  
...  

Soft Matter ◽  
2019 ◽  
Vol 15 (2) ◽  
pp. 159-165 ◽  
Author(s):  
Karthika Suresh ◽  
Marleen Häring ◽  
Guruswamy Kumaraswamy ◽  
David Díaz Díaz

The linear response of alginate-phenyl boronic acid (Alg-PBA) esters shows a universal, composition-independent viscoelastic fluid-like behaviour. However, their high strain behaviour is very sensitive to composition.


2018 ◽  
Vol 7 (4.5) ◽  
pp. 428
Author(s):  
Lolakshi Mahesh Kumar ◽  
Badekai Ramachandra Bhat

Pincer complexes with iron as active metal center were synthesized to study their catalytic activity in Suzuki-Miyaura coupling reactions. Tridentate pincer ligand was synthesized by the reaction of diphenylchlorophosphine with m-aminophenol and m-phenylenediamine respectively in a 2:1 ratio in the presence of triethylamine as a base and tetrahydrofuran as solvent media. The resultant ligand was complexed with FeSO4 to obtain PCP complexes, C-1 with O and N atoms in the side arms and C-2 with both N atoms in the side arms. The synthesized complexes were examined for their C-C coupling efficiency in cross-coupling between phenyl boronic acid and para substituted halobenzenes. The research study aims to provide an alternative approach to the Pd catalyzed cross coupling methods, an otherwise subjugated method to obtain cross-coupled products. Also the study implores on the effect of variation in the side arm atom relating to the donating ability of the ligand and thereby relatively affecting the coupling yield of the catalysts.  


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