82607-54-3Relevant academic research and scientific papers
Palladium-Catalyzed Regioselective C-Benzylation via a Rearrangement Reaction: Access to Benzyl-Substituted Anilines
Amézquita-Valencia, Manuel,Alper, Howard
supporting information, p. 16774 - 16778 (2016/11/17)
An unprecedented C-benzylation rearrangement reaction, catalyzed by palladium, is reported. The reaction proceeds by rearrangement leading to the direct synthesis of para or ortho benzyl-substituted N-methylanilines. The product is obtained in high regioselectivity, without the need to use a ligand for the catalytic process.
LiBF4-catalyzed formation of fused pyrano- and furanobenzopyrans
Yadav,Reddy,Madhuri, Ch,Sabitha, G,Jagannadh, B,Kumar,Kunwar
, p. 6381 - 6384 (2007/10/03)
Lithium tetrafluoroborate efficiently catalyzes an unusual cyclization of o-hydroxybenzaldimines with 2,3-dihydrofuran and 3,4-dihydro-2H-pyran at ambient temperature to afford a class of new pyrano- and furanobenzopyran derivatives in excellent yields with high diastereoselectivity.
