1177023-47-0Relevant articles and documents
Tunable and Diastereoselective Br?nsted Acid Catalyzed Synthesis of β-Enaminones
Kang, Ye-Won,Cho, Yu Jin,Han, Seung Jin,Jang, Hye-Young
supporting information, p. 272 - 275 (2016/02/03)
The Br?nsted acid catalyzed Meyer-Schuster reaction of hemiaminals was studied for the stereoselective synthesis of β-enaminones. Hemiaminals were formed from propargyl aldehydes (or the oxidation of propargyl alcohols) and amines in the presence of Br?ns
Nickel-catalyzed formation of a carbon-nitrogen bond at the β position of saturated ketones
Ueno, Satoshi,Shimizu, Ryosuke,Kuwano, Ryoichi
supporting information; experimental part, p. 4543 - 4545 (2009/10/30)
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