scholarly journals Front Cover: Size-Exclusion Borane-Catalyzed Domino 1,3-Allylic/Reductive Ireland-Claisen Rearrangements: Impact of the Electronic and Structural Parameters on the 1,3-Allylic Shift Aptitude (Chem. Eur. J. 9/2019)

2019 ◽  
Vol 25 (9) ◽  
pp. 2097-2097
Author(s):  
Dániel Fegyverneki ◽  
Natália Kolozsvári ◽  
Dániel Molnár ◽  
Orsolya Egyed ◽  
Tamás Holczbauer ◽  
...  
2018 ◽  
Vol 25 (9) ◽  
pp. 2179-2183 ◽  
Author(s):  
Dániel Fegyverneki ◽  
Natália Kolozsvári ◽  
Dániel Molnár ◽  
Orsolya Egyed ◽  
Tamás Holczbauer ◽  
...  

2019 ◽  
Vol 25 (9) ◽  
pp. 2100-2100
Author(s):  
Dániel Fegyverneki ◽  
Natália Kolozsvári ◽  
Dániel Molnár ◽  
Orsolya Egyed ◽  
Tamás Holczbauer ◽  
...  

Amylase ◽  
2019 ◽  
Vol 3 (1) ◽  
pp. 1-18 ◽  
Author(s):  
Wei Ping Quek ◽  
Wenwen Yu ◽  
Glen P. Fox ◽  
Robert G. Gilbert

Abstract In brewing, amylases are key enzymes in hydrolyzing barley starch to sugars, which are utilized in fermentation to produce ethanol. Starch fermentation depends on sugars produced by amylases and starch molecular structure, both of which vary with barley grain size. Grain size is a major industrial specification for selecting barley for brewing. An in-depth study is given of how enzyme activity and starch structure vary with grain size, the impact of these factors on fermentable sugar production, and the underlying mechanisms. Micro-malting and mashing experiments were based on commercial methodologies. Starch molecular structural parameters were obtained using size-exclusion chromatography, and fitted using biosynthesis-based models. Correlation analysis using the resulting parameters showed larger grain sizes contained fewer long amylopectin chains, higher amylase activities and soluble protein level. Medium grain sizes released most sugars during mashing, because of higher starch utilization from the action of amylases, and shorter amylose chains. As starch is the substrate for amylase-driven fermentable sugars production, measuring its structure should be a prime indication for mashing performance, and should be used as an industry specification when selecting barley grains for brewing.


e-Polymers ◽  
2003 ◽  
Vol 3 (1) ◽  
Author(s):  
Benjamin Carbonnier ◽  
Ludovic Janus ◽  
André Deratani ◽  
Michel Morcellet

Abstract This paper describes the preparation of a chiral stationary phase based on a 2-hydroxypropyl-β-cyclodextrin polymer coated on porous silica. This method requires first the synthesis of a water-soluble cyclodextrin polymer carried out by the polycondensation of 2-hydroxypropyl-β-cyclodextrin with epichlorohydrin under controlled conditions. In the second step, the obtained copolymer was immobilised onto the porous silica surface by physisorption. The macromolecular features of the copolymer were investigated by size exclusion chromatography coupled with a multiple angle laser-light scattering detector. The evolution of the structural parameters of the modified silica beads (specific surface area and pore size distribution) was determined using a nitrogen adsorption method. The enantio-separation capability of the coated silica phase was evaluated for different polycyclic molecules. It was found that the enantioselectivity was strongly influenced by the geometry and shape of the solutes under study and the presence of an acidic modifier in the mobile phase.


Polymers ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1510 ◽  
Author(s):  
Zouganelis ◽  
Choinopoulos ◽  
Goulas ◽  
Pitsikalis

The cationic statistical copolymerization of n-butyl (be) and 2-chloroethyl vinyl ether (CEVE), is efficiently conducted using bis(η5-cyclopentadienyl)dimethyl zirconium (Cp2ZrMe2) in combination with tetrakis(pentafluorophenyl)borate dimethylanilinum salt [B(C6F5)4]–[Me2NHPh]+, as an initiation system. The reactivity ratios are calculated using both linear graphical and non-linear methods. Structural parameters of the copolymers are obtained by calculating the dyad sequence fractions and the mean sequence length, which are derived using the monomer reactivity ratios. The glass transition temperatures (Tg) of the copolymers are measured by Differential Scanning Calorimetry (DSC), and the results are compared with predictions based on several theoretical models. The statistical copolymers are further employed as scaffolds for the synthesis of graft copolymers having poly(vinyl ether)s as a backbone and either poly(ε-caprolactone) (PCL) or poly(l-lactide) (PLLA) as side chains. Both the grafting “onto” and the grafting “from” methodologies are employed. The reaction sequence is monitored by Size Exclusion Chromatography (SEC), NMR and IR spectroscopies. The advantages and limitations of each approach are thoroughly examined.


Sign in / Sign up

Export Citation Format

Share Document