UOP announces price increase for solid phosphoric acid catalysts for refining and petrochemicals

2008 ◽  
Vol 2008 (7) ◽  
pp. 5
2015 ◽  
Vol 8 (3) ◽  
pp. 1263-1274 ◽  
Author(s):  
Zhi-bo Zhang ◽  
Qiang Lu ◽  
Xiao-ning Ye ◽  
Ti-peng Wang ◽  
Xian-hua Wang ◽  
...  

1968 ◽  
Vol 8 (4) ◽  
pp. 268-275
Author(s):  
Y USOV ◽  
Y SKVORTSOVA ◽  
K VAISTUB

2016 ◽  
Vol 14 (11) ◽  
pp. 3031-3039 ◽  
Author(s):  
Luis Simón ◽  
Robert S. Paton

An explanation of why confined imidodiphosphoric acid catalyst succeeds where other chiral phosphoric acid catalysts fail.


Author(s):  
Alemayehu Gashaw ◽  
Dereje Kebebew Debeli ◽  
Meseret Chemeda

: The C-H and N-H functionalization of indoles is an interesting area of research that has a useful impact on organic synthesis due to the availability of chiral indole scaffolds in the discovery of drugs, synthetic bioactive compounds, and natural products. The chiral phosphoric acid catalysts (CPAs) have proven to be a powerful and versatile class of enantioselective organocatalysts. Many asymmetric syntheses of organic compounds have been carried out with these catalysts in C–C and C-N bond formation reactions, and great progress has been reported. By 2011, several reviews were published covering some important topics and recent achievements in this field. Therefore, in this review, the most recent advances, research breakthroughs with key examples involving mechanisms of CPA-catalyzed C-H and N-H functionalization of indoles to form central chirality via Friedel Crafts, Michael type, and rearrangement reactions were reviewed and reported.


2018 ◽  
Vol 16 (8) ◽  
pp. 1367-1374 ◽  
Author(s):  
Abdul Rahman ◽  
En Xie ◽  
Xufeng Lin

An enantioselective aza-Friedel–Crafts reaction of trifluoromethyl dihydrobenzoazepinoindoles with pyrroles or indoles catalyzed by a chiral spirocyclic phosphoric acid was developed.


2014 ◽  
Vol 1025-1026 ◽  
pp. 651-655
Author(s):  
Zhe Wang ◽  
Zhen An

Southern pine (Pinus sp.) is liquefied by microwave heating and PEG/lower alcohols mixtures in the presence of various acid catalysts at 150 °C. The reaction time is of 15 min, and the liquefaction solvent to wood ratio is of 2:1. The mixing of lower alcohols such as ethanol with PEG had a strong effect on the liquefaction process, especially for the liquefaction ratio. The catalyst, phosphoric acid, could improve the liquefaction yield and the value of hydroxyl in the biomass liquefaction process. Consequently, the use of PEG/ethanol mixtures and a catalyst of phosphoric acid was benefit to improve liquefaction efficiency and utilization of liquefied products.


Chirality ◽  
2019 ◽  
Vol 31 (8) ◽  
pp. 592-602
Author(s):  
Xiaoxue Tang ◽  
Hualing He ◽  
Xiantao Fang ◽  
Zexu Chang ◽  
Jon C. Antilla

2016 ◽  
Vol 45 (11) ◽  
pp. 1300-1303 ◽  
Author(s):  
Naoki Yoneda ◽  
Akira Matsumoto ◽  
Keisuke Asano ◽  
Seijiro Matsubara

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