New Views on the Reaction of Primary Amine and Aldehyde from DFT Study

2015 ◽  
Vol 119 (18) ◽  
pp. 4252-4260 ◽  
Author(s):  
Yun-qiao Ding ◽  
Yue-zhi Cui ◽  
Tian-duo Li
Keyword(s):  
ChemCatChem ◽  
2017 ◽  
Vol 9 (24) ◽  
pp. 4450-4450
Author(s):  
Karan Bobuatong ◽  
Hidehiro Sakurai ◽  
Masahiro Ehara

RSC Advances ◽  
2016 ◽  
Vol 6 (73) ◽  
pp. 68695-68704 ◽  
Author(s):  
Yiming Ren ◽  
Ruizhu Yang ◽  
Lang Shao ◽  
Hao Tang ◽  
Shaofei Wang ◽  
...  

Phosphoramide-modified SBA-15 materials were prepared via a two-step process involving: (1) the synthesis of phosphoramide via amidation of phosphoryl chloride with a primary amine and (2) modification of the phosphoramide onto SBA-15.


ChemCatChem ◽  
2017 ◽  
Vol 9 (24) ◽  
pp. 4490-4500 ◽  
Author(s):  
Karan Bobuatong ◽  
Hidehiro Sakurai ◽  
Masahiro Ehara

2009 ◽  
Author(s):  
Manuel Fernández-Gómez ◽  
Amparo Navarro ◽  
MªPaz Fernández-Liencres ◽  
Mónica Moral ◽  
José Manuel Granadino-Roldán ◽  
...  

2020 ◽  
Author(s):  
Rémi Blieck ◽  
Sebastien Lemouzy ◽  
Marc Taillefer ◽  
Florian Monnier

A dual copper/enamine catalytic system is found to enable an intermolecular enantioselective α-addition of various carbonyl nucleophiles to allenamides. Secondary amine catalysts allowed the highly enantioselective addition of aldehydes, while using primary amine catalysts led to the enantioselective addition of ketoester nucleophiles. The process was found to be highly regio-, stereo- and enantio-selective and represented the first allene hydrofunctionalization using an synergistic catalysis involving copper


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