carbonylation reaction
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Recognizing the Important Role of Surface Barriers in MOR Zeolite Catalyzed DME Carbonylation Reaction

ACS Catalysis ◽  
2021 ◽  
pp. 1-7
Author(s):  
Kaipeng Cao ◽  
Dong Fan ◽  
Mingbin Gao ◽  
Benhan Fan ◽  
Nan Chen ◽  
...  
Keyword(s):  
Carbonylation Reaction ◽  
Surface Barriers

An innovative spectroscopic approach for qualitative and quantitative evaluation of Mb-CO from myoglobin carbonylation reaction through chemometrics methods

2021 ◽  
pp. 120602
Author(s):  
Felipe R. P. Mansoldo ◽  
Emanuela Berrino ◽  
Paolo Guglielmi ◽  
Simone Carradori ◽  
Fabrizio Carta ◽  
...  
Keyword(s):  
Quantitative Evaluation ◽  
Qualitative And Quantitative ◽  
Carbonylation Reaction

Effect of N-Methyl-2-pyrrolidone on Al Distribution in MOR and Enhanced Activity in DME Carbonylation Reaction

2021 ◽  
Vol 50 (8) ◽  
pp. 1562-1565
Author(s):  
Mingxue Shi ◽  
Yaquan Wang ◽  
Chao Sun ◽  
Taotao Zhao ◽  
Jingjing Zhao ◽  
...  
Keyword(s):  
Carbonylation Reaction ◽  
Enhanced Activity ◽  
Al Distribution

Solar photothermal catalytic effect promotes carbonylation reaction based on palladium doped g-C3N4 catalyst

2021 ◽  
Vol 137 ◽  
pp. 111194
Author(s):  
Panting Lu ◽  
Wenxing Chen ◽  
Wangyang Lu
Keyword(s):  
Catalytic Effect ◽  
Carbonylation Reaction

scholarly journals Mechanism of CO2 reduction in carbonylation reaction promoted by ionic liquid additives: A computational and experimental study

2021 ◽  
Author(s):  
Kai-Lun Bi ◽  
Bao-Hua Xu ◽  
Wei-Lu Ding ◽  
Li-Jun Han ◽  
Lin Ji
Keyword(s):  
Experimental Study ◽  
Ionic Liquid ◽  
Co2 Reduction ◽  
Carbonylation Reaction

Study on the deactivation process of dimethyl ether carbonylation reaction over Mordenite catalyst

Fuel ◽  
2021 ◽  
Vol 286 ◽  
pp. 119480
Author(s):  
Xiaosheng Wang ◽  
Ranjia Li ◽  
Changchun Yu ◽  
Yuxiang Liu ◽  
Chunming Xu ◽  
...  
Keyword(s):  
Dimethyl Ether ◽  
Carbonylation Reaction ◽  
Deactivation Process

scholarly journals Reaction Mechanism of Pd‐Catalyzed “CO‐Free” Carbonylation Reaction Uncovered by In Situ Spectroscopy: The Formyl Mechanism

2020 ◽  
Author(s):  
Robert Geitner ◽  
Andrei Gurinov ◽  
Tianbai Huang ◽  
Stephan Kupfer ◽  
Stefanie Gräfe ◽  
...  
Keyword(s):  
Reaction Mechanism ◽  
In Situ Spectroscopy ◽  
Carbonylation Reaction

scholarly journals Reaction Mechanism of Pd‐Catalyzed “CO‐Free” Carbonylation Reaction Uncovered by In Situ Spectroscopy: The Formyl Mechanism

2020 ◽  
Author(s):  
Robert Geitner ◽  
Andrei Gurinov ◽  
Tianbai Huang ◽  
Stephan Kupfer ◽  
Stefanie Gräfe ◽  
...  
Keyword(s):  
Reaction Mechanism ◽  
In Situ Spectroscopy ◽  
Carbonylation Reaction

Bio- and medicinally compatible α-amino acid modification via merging photo-redox and N-heterocyclic carbene catalysis

2020 ◽  
Author(s):  
Jie Feng ◽  
Ding Du ◽  
Kuili Zhang ◽  
Jian Gao ◽  
Tao Lu ◽  
...  
Keyword(s):  
Amino Acid ◽  
Chemical Modification ◽  
Late Stage ◽  
Chemical Biology ◽  
Acid Modification ◽  
Carbonylation Reaction ◽  
Direct Pathway ◽  
Amino Acid Modification ◽  
Stage Synthesis

An NHC and photo-redox co-catalyzed α-amino acid decarboxylative carbonylation reaction was presented here. This method displayed good scope generality, providing an easy and direct pathway to access various downstream α-amino ketones from readily accessible starting materials under bio- and medicinally compatible conditions. Moreover, this strategy is appealing to chemical biology since it has great potential for chemical modification of peptides or late-stage synthesis of keto-peptides.

Bio- and medicinally compatible α-amino acid modification via merging photo-redox and N-heterocyclic carbene catalysis

2020 ◽  
Author(s):  
Jie Feng ◽  
Ding Du ◽  
Kuili Zhang ◽  
Jian Gao ◽  
Tao Lu ◽  
...  
Keyword(s):  
Amino Acid ◽  
Chemical Modification ◽  
Late Stage ◽  
Chemical Biology ◽  
Acid Modification ◽  
Carbonylation Reaction ◽  
Direct Pathway ◽  
Amino Acid Modification ◽  
Stage Synthesis

An NHC and photo-redox co-catalyzed α-amino acid decarboxylative carbonylation reaction was presented here. This method displayed good scope generality, providing an easy and direct pathway to access various downstream α-amino ketones from readily accessible starting materials under bio- and medicinally compatible conditions. Moreover, this strategy is appealing to chemical biology since it has great potential for chemical modification of peptides or late-stage synthesis of keto-peptides.

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