Application of 4719-04-4, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 4719-04-4, Name is 2,2′,2”-(1,3,5-Triazinane-1,3,5-triyl)triethanol, SMILES is OCCN1CN(CCO)CN(CCO)C1, belongs to alcohols-buliding-blocks compound. In a article, author is Dong, Mengxian, introduce new discover of the category.
Highly enantioselective transfer hydrogenation catalyzed by diasteromeric mixtures of axially chiral (aR,S)- and (aS,S)-Biscarbolines
The mixtures of axially chiral (aR,S)- and (aS,S)-biscarboline alcohols were firstly used as catalysts in enantioselective 1,2- and 1,4-transfer hydrogenations of ketimines and beta-enamino esters, respectively. This mixed axially chiral catalysts exhibited excellent enantioselectivity (up to 98%ee) in the transfer hydrogenations under mild reaction conditions. (C) 2021 Elsevier Ltd. All rights reserved.
Application of 4719-04-4, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 4719-04-4 is helpful to your research.
Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts