162706-25-4Relevant articles and documents
Nickel-Catalyzed system for the cross-coupling of alkenyl methyl ethers with grignard reagents under mild conditions
Hostier, Thomas,Neouchy, Zeina,Ferey, Vincent,Gomez Pardo, Domingo,Cossy, Janine
supporting information, p. 1815 - 1818 (2018/04/14)
A nickel-catalyzed cross-coupling of alkenyl methyl ethers with Grignard reagents, under mild conditions, is described. These conditions allowed access to various stilbenes and heterocyclic stilbenic derivatives as well as to a potential anticancer agent DMU-212.
Enol ethers as carbonyl surrogates in a modification of the Povarov synthesis of 3-aryl quinolines and their anti-Toxoplasma activity
Brown, Carla E.,McNulty, James,Bordón, Claudia,Yolken, Robert,Jones-Brando, Lorraine
supporting information, p. 5951 - 5955 (2016/07/06)
A novel method for the preparation of 2-carboxyl-3-aryl quinoline derivatives from anilines, ethyl glyoxalate and enol ethers as phenylacetaldehyde surrogates is reported. The three-component coupling reaction occurs rapidly under mild conditions in dichl
Microwave-assisted in situ deprotection and ω-methoxylation of TMS-protected aryl alkynes
Wettergren, Jenny,Minidis, Alexander B. E.
, p. 7611 - 7612 (2007/10/03)
Using microwave technology, rapid ω-methoxylation of aryl alkynes is possible.
