1311378-59-2

Upstream product

• 1388625-05-5 C₁₇H₁₇NO 
• 1311378-46-7 (E)-benzaldehyde O-(1,3-diphenylprop-2-yn-1-yl)oxime 
• 1388624-49-4 4-methylbenzaldehyde O-[1,3-bis(4-methylphenyl)prop-2-yn-1-yl]oxime 
• 925428-19-9 2-(1,3-diphenylprop-2-ynyloxy)isoindoline-1,3-dione 
• 910896-82-1 O-(1,3-diphenylprop-2-yn-1-yl)hydroxylamine 

Relevant academic research and scientific papers

Copper-catalyzed skeletal rearrangement of o -propargylic aryloximes into four-membered cyclic nitrones - Chirality transfer and mechanistic insight

Copper-catalyzed skeletal rearrangement of O-propargylic aryloximes (E)-1 were carried out to afford the corresponding four-membered cyclic nitrones 2 in good to excellent yields. The optimal reactions conditions of the highly regioselective reactions inv

Regioselective transformation of O-propargylic arylaldoximes to four-membered cyclic nitrones by copper-catalyzed skeletal rearrangement

(E)-O-Propargylic arylaldoximes were regioselectively converted, in the presence of copper catalysts, into their corresponding four-membered cyclic nitrones in good to excellent yields. The reactions proceeded via a tandem [2,3]-rearrangement and 4π-elect