80312-17-0Relevant articles and documents
Chiral Metal Salts as Ligands for Catalytic Asymmetric Mannich Reactions with Simple Amides
Yamashita, Yasuhiro,Noguchi, Aika,Fushimi, Seiya,Hatanaka, Miho,Kobayashi, Shū
supporting information, p. 5598 - 5604 (2021/05/06)
Catalytic asymmetric Mannich reactions of imines with weakly acidic simple amides were developed using a chiral potassium hexamethyldisilazide (KHMDS)-bis(oxazoline) potassium salt (K-Box) catalyst system. The desired reactions proceeded to afford the tar
Precipitation-driven self-sorting of imines
Lirag, Rio Carlo,Osowska, Karolina,Miljanic, Ognjen S.
supporting information; experimental part, p. 4847 - 4850 (2012/07/14)
Judicious choice of precipitation conditions can lead to self-sorting of equilibrating mixtures of aromatic aldehydes and substituted anilines into a handful of imine products. The selectivity of this process is caused by the solubility differences among possible imines in the EtOH-H2O solvent mixtures used in precipitation.
One-pot synthesis and fluorescence properties of 2-arylquinolines
Sueki, Shunsuke,Okamoto, Chiharu,Shimizu, Isao,Seto, Keisuke,Furukawa, Yukio
supporting information; experimental part, p. 385 - 390 (2010/07/09)
The one-pot synthesis of 2-arylquinoline with arylamines, arylaldehyde, and 1,1-diethoxyethane were studied using a catalytic amount ytterbium triflate. Various 2-arylquinolines showed fluorescence properties and the fluorescence was quenched by introduci