144632-52-0Relevant articles and documents
Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt
Yoshida, Masanori,Sato, Atsushi,Hara, Shoji
experimental part, p. 3031 - 3036 (2010/09/06)
Enantioselective Michael addition of aldehydes to nitroalkenes was successfully carried out by asymmetric catalysis with l-phenylalanine lithium salt, giving γ-nitroaldehydes in good yields with high enantioselectivity.
Michael additions of aldehydes and ketones to β-nitrostyrenes in an ionic liquid
Kotrusz, Peter,Toma, Stefan,Schmalz, Hans-Guenther,Adler, Andreas
, p. 1577 - 1583 (2007/10/03)
Michael additions of different aldehydes and ketones to β-nitrostyrene and 2-(β-nitrovinyl)thiophene in 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim]PF6) were studied. β-Nitrostyrene was a better acceptor than 2-(β-nitrovinyl)thiophen