One pot cascade biosynthesis of d-allulose from d-glucose and its kinetic modelling

2022 ◽  
Vol 248 ◽  
pp. 117167
Author(s):  
Xiaoyan Chen ◽  
Fan Wang ◽  
Qiang Yu ◽  
Shijie Liu ◽  
Wen Wang ◽  
...  
Keyword(s):  
2019 ◽  
Vol 8 (1) ◽  
pp. 516-524 ◽  
Author(s):  
Luma Sh. Al-Saadi ◽  
Valentine C. Eze ◽  
Adam P. Harvey

Abstract A “reactive coupling” process for one-pot transesterification of rapeseed oil into fatty acid methyl esters (FAME) for biodiesel, and in situ acetalisation of the glycerol by-product to solketal was investigated by both an experimental and a kinetic modelling approach. The aim was to develop a process with a more valuable co-products than glycerol, and to minimise glycerol production. The results showed that a one-stage reactive coupling achieved a solketal yield of 39.5 ± 5.1% and FAME yield of 99% after 8 h at 10:7:1 of methanol: acetone: oil molar ratio. However, based on these results and the predictions of the kinetic model developed, a “two-stage” reactive coupling process was investigated, in which some of the acetone was added later in the process. The two-stage process was demonstrated to achieve up to 98 ± 0.5% FAME and 82 ± 4% solketal yields under the same operating conditions.


Author(s):  
E. Sekman ◽  
G. Varank ◽  
A. Demir ◽  
S. Top ◽  
M. S. Bilgili

2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.


Sign in / Sign up

Export Citation Format

Share Document