15205-68-2Relevant academic research and scientific papers
A new method using 2-chloro-4,6-dimethoxy-1,3,5-triazine for facile elimination of dimethylamino group in Eschenmoser's methylenation for synthesis of α,β-unsaturated esters
Yamada, Kohei,Masaki, Kazumasa,Hagimoto, Yuri,Kamiya, Seina,Kunishima, Munetaka
supporting information, p. 1758 - 1760 (2013/03/29)
A facile one-step method for the elimination of the dimethylamino group in Eschenmoser's methylenation has been developed using a combination of 2-chloro-4,6-dimethoxy-1,3,5-triazine and triethylamine. The chemoselective elimination of the dimethylamino group occurred in compounds possessing either a diethylamino group or an alkylsulfanyl group.
(METH)ACRYLIC ACID ESTER, ACTIVATION ENERGY RAY CURING COMPOSITION, AND INKJET RECORDING INK
-
Paragraph 0105; 0106; 0107; 0153; 0154, (2013/06/26)
(Meth)acrylic acid ester, which contains one or more partial structures each represented by the following formula 1 in a molecule thereof, wherein the partial structure is a urethane structure which does not have a hydrogen atom directly bonded to a nitrogen atom of the following formula 1: where the nitrogen atom is not bonded to a hydrogen atom.
