1036999-75-3Relevant academic research and scientific papers
Photochemical electrocyclization of α,β-unsaturated anilides to give zwitterionic intermediates which eliminate carboxylate and phenolate leaving groups
Jia, Jinli,Steinmetz, Mark G.,Shukla, Ruchi,Rathore, Rajendra
, p. 4621 - 4623 (2008/09/21)
α,β-Unsaturated anilides bearing allylic leaving groups undergo photochemical electrocyclic ring closure to produce zwitterionic intermediates which eliminate carboxylate and phenolate leaving groups.
Photochemical elimination of leaving groups from zwitterionic intermediates generated via electrocyclic ring closure of α,β-unsaturated anilides
Jia, Jinli,Sarker, Majher,Steinmetz, Mark G.,Shukla, Ruchi,Rathore, Rajendra
scheme or table, p. 8867 - 8879 (2009/04/04)
(Chemical Equation Presented) Methacrylanilides, ArN(CH3) COC(CH2LG)=CH2, with allylic leaving groups (LG - = BocAla, PhCO2-, PhCH2CO 2-, PhO-) u
