Add time:08/15/2019         Source:sciencedirect.com

Two N-benzyl imines are designed to allow for carbon–carbon bond formations at the aminated benzylic positions. Direct benzylic arylation reactions of N-benzylxanthone imine with aryl chlorides proceed under palladium catalysis in the presence of cesium hydroxide, yielding the corresponding benzhydrylamine derivatives. Alkylation reactions of N-benzyldi-1-naphthyl ketone imine with alkyl halides in the presence of potassium tert-butoxide afford the corresponding 1-phenylalkylamines in high yields. Conjugate addition of N-benzyldi-1-naphthyl ketone imine is also described.

We also recommend Trading Suppliers and Manufacturers of N-(1-NAPHTHYL)-3-AMINOPROPANESULFONIC ACID SODIUM SALT (cas 104484-71-1). Pls Click Website Link as below: cas 104484-71-1 suppliers