13858-92-9Relevant academic research and scientific papers
On-water magnetic NiFe2O4 nanoparticle-catalyzed Michael additions of active methylene compounds, aromatic/aliphatic amines, alcohols and thiols to conjugated alkenes
Payra, Soumen,Saha, Arijit,Banerjee, Subhash
, p. 95951 - 95956 (2016/10/25)
Here, we have demonstrated the Michael addition of active methylene compounds, aromatic/aliphatic amines, thiols and alcohols to conjugated alkenes using magnetic nano-NiFe2O4 as reusable catalyst in water. Nano-NiFe2O4 efficiently catalyzed the formation of C-C and C-X (X = N, S, O etc.) bond through 1,4-addition reactions.
Conjugate addition nitro-Mannich reaction of carbon and heteroatom nucleophiles to nitroalkenes
Anderson, James C.,Kalogirou, Andreas S.,Tizzard, Graham J.
, p. 9337 - 9351 (2015/03/05)
The conjugate addition nitro-Mannich reactions of ethyl-β-nitroacrylate (1) and β-nitrostyrene (2) with electron rich aromatic nucleophiles, stabilized carbanions, alcohols, amines, thiols, and diphenyl phosphine oxide were investigated. The one pot conju
β-Alkoxy-substituted phenethylamines: A family of compounds potentially active at the dopamine and α-adrenergic receptors
Katerinopoulos,Tagmatarchis,Zaponakis,Kefalakis,Kordatos,Spyrakis,Thermos
, p. 949 - 954 (2007/10/03)
A series of β-alkoxy-substituted phenethylamines were synthesized and tested for their affinity at the D1 and D2 dopaminergic receptors and the α1 and α2 adrenoceptors. None of the tested compounds exhibited D2 receptor af
