scholarly journals One-Pot Synthesis of Mesoporous Ni–Ti–Al Ternary Oxides: Highly Active and Selective Catalysts for Steam Reforming of Ethanol

2017 ◽  
Vol 9 (7) ◽  
pp. 6079-6092 ◽  
Author(s):  
Alexandre A. S. Gonçalves ◽  
Patrícia B. Faustino ◽  
José M. Assaf ◽  
Mietek Jaroniec
Keyword(s):  
Steam Reforming ◽  
One Pot ◽  
One Pot Synthesis ◽  
Highly Active ◽  
Steam Reforming Of Ethanol ◽  
Ternary Oxides

Highly active and stable Ni supported on CNTs-SiO 2 fiber catalysts for steam reforming of ethanol

2017 ◽  
Vol 160 ◽  
pp. 185-195 ◽  
Author(s):  
Natthawan Prasongthum ◽  
Rui Xiao ◽  
Huiyan Zhang ◽  
Noritatsu Tsubaki ◽  
Paweesuda Natewong ◽  
...  
Keyword(s):  
Steam Reforming ◽  
Highly Active ◽  
Steam Reforming Of Ethanol

scholarly journals Divergent [{ONNN}Mg–Cl] complexes in highly active and living lactide polymerization

2017 ◽  
Vol 8 (8) ◽  
pp. 5476-5481 ◽  
Author(s):  
Tomer Rosen ◽  
Israel Goldberg ◽  
Wanda Navarra ◽  
Vincenzo Venditto ◽  
Moshe Kol
Keyword(s):  
Diblock Copolymer ◽  
One Pot ◽  
One Pot Synthesis ◽  
Highly Active ◽  
Lactide Polymerization

The longest PLA stereo-diblock copolymer by one-pot synthesis.

scholarly journals Aerobic synthesis of N-sulfonylamidines mediated by N-heterocyclic carbene copper(I) catalysts

2020 ◽  
Vol 16 ◽  
pp. 482-491
Author(s):  
Faïma Lazreg ◽  
Marie Vasseur ◽  
Alexandra M Z Slawin ◽  
Catherine S J Cazin
Keyword(s):  
One Pot ◽  
Mild Conditions ◽  
One Pot Synthesis ◽  
Highly Active ◽  
Copper Acetylide ◽  
The One

A new catalytic strategy for the one-pot synthesis of N-sulfonylamidines is described. The cationic copper(I) complexes were found to be highly active and efficient under mild conditions in air and in the absence of solvent. A copper acetylide is proposed as key intermediate in this transformation.

2-Phenyl-2,3-dihydrobenzo[d]thiazole: A Mild, Efficient, and Highly Active in situ Generated Chemoselective Reducing Agent for the One-Pot Synthesis of 5-Monoalkylbarbiturates in Water

Synlett ◽  
2017 ◽  
Vol 29 (04) ◽  
pp. 477-482 ◽  
Author(s):  
Dibakar Deka ◽  
Subarna Kalita
Keyword(s):  
Reducing Agent ◽  
High Yield ◽  
Purification Process ◽  
Reaction Conditions ◽  
One Pot ◽  
One Pot Synthesis ◽  
Highly Active ◽  
The One ◽  
Operational Simplicity

A metal- and catalyst-free reductive alkylation protocol for the one-pot synthesis of 5-monoalkylbarbiturates from barbituric acids and aldehydes using the in situ generated chemoselective reducing agent 2-phenyl-2,3-dihydrobenzo[d]thiazole from 2-aminothiophenol and benzaldehyde is described. The notable advantages of the protocol are operational simplicity, mild reaction conditions, high yield, short reaction time, and simple workup and purification process which make it highly attractive.

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