1193067-50-3Relevant academic research and scientific papers
Bioinspired Catalysis: Self-Assembly of a Protein and DNA as a Catalyst for the Aldol Reaction in Aqueous Media
Liu, Hongxin,Li, Guangxun,Wang, Ying-Wei,Zhang, Shiqi,Tang, Zhuo
, p. 560 - 565 (2018)
An interesting bioinspired catalyst formed from readily available DNA and a protein through electrostatic interaction in situ proved to be efficient in catalyzing aldol reactions under mild conditions in water. By using a self-assembling catalytic system
Zinc(II) mediated asymmetric aldol condensation catalyzed by chiral aziridine ligands
Pieczonka, Adam M.,Jarzyński, Szymon,Wujkowska, Zuzanna,Les?niak, Stanis?aw,Rachwalski, Micha?
, p. 6506 - 6507 (2015)
Exploration of chiral aziridine ethers and aziridine alcohols as ligands for the Zn(II) catalyzed enantioselective direct aldol condensations reaction is described. The reaction of acetone with NO2-substituted aromatic aldehydes in the presence
Direct asymmetric aldol condensation catalyzed by aziridine semicarbazide zinc(II) complexes
Pieczonka, Adam M.,Le?niak, Stanis?aw,Rachwalski, Micha?
, p. 2373 - 2375 (2014/05/06)
Previously obtained semicarbazides derived from N-triphenylmethyl- aziridine-2-carbohydrazide were explored as ligands in Zn(II) catalyzed diastereo- and enantioselective direct aldol reactions. Complexes of aziridine-semicarbazides with Zn(II) were effic
Efficient asymmetric aldol reaction catalyzed by polyvinylidene chloride-supported ionic liquid/l-proline catalyst system
Zhang, Xuan,Zhao, Wenshan,Qu, Chengke,Yang, Lili,Cui, Yuanchen
experimental part, p. 468 - 473 (2012/07/28)
A series of polyvinylidene chloride (PVDC)-supported ionic liquids were derived from 4-dimethylaminopyridine and used together with l-proline in water as efficient asymmetric organocatalysts for direct asymmetric aldol reactions between cyclohexanone and
N-prolinylanthranilamide pseudopeptides as bifunctional organocatalysts for asymmetric aldol reactions
Pearson, Anthony J.,Panda, Santanu
supporting information; experimental part, p. 5548 - 5551 (2011/12/05)
Proline anthranilamide-based pseudopeptides were shown to be effective organocatalysts for enantioselective direct aldol reactions of a selection of aldehydes with various ketones with excellent yield, enantioselectivity up to 99% and anti to syn diastere
A novel trifunctional organocatalyst for the asymmetric aldol reaction: A facile enantioselective synthesis of β-hydroxyketones
Subba Reddy,Bhavani,Raju,Yadav
experimental part, p. 881 - 886 (2011/08/09)
A new l-prolinamide trifunctional catalyst has been developed for the enantioselective aldol reaction of various aromatic and aliphatic aldehydes with acetone. This method provides high yields of β-hydroxyketones (up to 90%) with good enantioselectivity (up to 92%) at a low catalyst loading (10 mol %).
