63509-18-2Relevant academic research and scientific papers
Ionic Liquid-Promoted Phospha-Michael Reaction: Convenient Access to β-Nitrophosphonates
Jayaprakash,Satheesh Krishna,Santhi Sudha,Bakthavatchala Reddy,Sreelakshmi,Kumar Reddy, K. Madhu,Suresh Reddy
, p. 2083 - 2091 (2015)
A convenient and mild procedure is developed for β-nitrophosphonates via phospha-Michael addition of phosphites to nitrostyrene at room temperature in the presence of 1,8-diazabicyclo-[5.4.0]undec-7-ene (DBU)-based ionic liquid [DBUH][OAc]. The operationa
Enantioselective conjugate addition of dialkyl phosphites to nitroalkenes
Rai, Vishal,Namboothiri, Irishi N.N.
scheme or table, p. 2335 - 2338 (2009/04/11)
The Michael addition of dialkyl phosphites to nitroalkenes in the presence of heterobimetallic (S)-(-)-aluminum lithium bis(binaphthoxide), ALB, complex provided β-nitrophosphonates, precursors to β-aminophosphonic acids, in good to excellent enantioselec
