1041177-05-2Relevant academic research and scientific papers
Copper-Catalyzed Aerobic Oxidations of 3-N-Hydoxyaminoprop-1-ynes to Form 3-Substituted 3-Amino-2-en-1-ones: Oxidative Mannich Reactions with a Skeletal Rearrangement
Kawade, Rahul Kisan,Tseng, Chang-Chin,Liu, Rai-Shung
, p. 13927 - 13931 (2016/02/18)
Cu-catalyzed aerobic oxidations of readily available 3-N-hydroxyaminopro-1-ynes with water, alcohols, or thiols to form diverse 3-substituted 3-amino-2-en-1-ones are described. The utility of this catalysis is manifested by a wide scope of applicable N-hydroxyl propargylamines and nucleophiles, thus enabling the design of one-pot cascade or two-step sequential reactions. Besides synthetic significances, such oxidative Mannich reactions are mechanistically interesting because structurally reorganized products were obtained. Our mechanistic studies reveal that the aerobic oxidations involve initial formation of nitrone intermediates, followed by the attack of nucleophiles. Herein, water and MeOH implement the conversion of nitrone intermediates to reaction products in two distinct pathways. Go Mannich! Cu-catalyzed aerobic oxidations of 3-N-hydroxyaminopro-1-ynes with water, alcohols, or thiols to form diverse 3-substituted 3-amino-2-en-1-ones are reported (see scheme). Such oxidative Mannich reactions are mechanistically interesting, because structurally reorganized products were obtained.
Cupric chloride promoted regioselective C-allylation of enaminones
Singh, Sarangthem Joychandra,Singh, Okram Mukherjee
, p. 3991 - 3994 (2008/09/20)
Regioselective allylation of enaminones using CuCl2 as the catalyst to give C-allylated products is reported for the first time. The C-allylated products undergo hydrolysis followed by a rearrangement yielding β-keto allyl enamides in excellent yields.
