943763-35-7Relevant academic research and scientific papers
Sodium hydride mediated cascade reaction towards the synthesis of 1,5-disubstituted uracil from cyanamides derived from Baylis-Hillman adducts
Nag,Yadav,Maulik,Batra
, p. 911 - 917 (2007/12/27)
The substituted cyanamides generated from Baylis-Hillman adducts afford 1,5-disubstituted uracils via a sodium hydride induced cascade reaction involving sequential intramolecular attack of the hydroxy group on the nitrile group, cyclization of the result
Amination of the Baylis-Hillman acetates in ethanol
Park, Young Sang,Cho, Min Young,Kwon, Young Bum,Yoo, Byung Woo,Yoon, Cheol Min
, p. 2677 - 2685 (2008/02/12)
Baylis-Hillman acetates in EtOH were substituted by various nitrogen nucleophiles to give the corresponding trisubstituted alkenes in high yields. Copyright Taylor & Francis Group, LLC.
