910541-65-0Relevant academic research and scientific papers
Enantioselective synthesis of nitrocyclopropanes via conjugate addition of bromomalonate to nitroalkenes catalyzed by Ni(II) complexes
Lee, Hyun Joo,Kim, Sun Mi,Kim, Dae Young
, p. 3437 - 3439 (2012/08/08)
A novel one-pot methodology for the catalytic enantioselective synthesis of highly functionalized nitrocyclopropanes promoted by chiral nickel complexes is developed. The treatment of bromomalonates with nitroalkenes under the mild reaction conditions aff
Stereoselective synthesis of functionalised cyclopropanes from nitroalkenes via an organocatalysed Michael-initiated ring-closure approach
Russo, Alessio,Lattanzi, Alessandra
experimental part, p. 1155 - 1157 (2010/10/20)
Synthetically useful nitrocyclopropanes are easily obtained via Michael addition of dimethyl bromomalonate to nitrostyrenes promoted by commercially available (S)-α,α-di-β-naphthlyl-2-pyrrolidinemethanol as the catalyst, followed by DABCO-mediated intramo
Highly enantioselective synthesis of nitrocyclopropanes via organocatalytic conjugate addition of bromomalonate to αβ-unsaturated nitroalkenes
Xuan,Nie,Dong,Zhang,Yan, Ming
supporting information; experimental part, p. 1583 - 1586 (2009/09/06)
Highly enantioselective synthesis of nitrocyclopropanes was achieved via the organocatalytic conjugate addition of dimethyl bromomalonate to nitroalkenes and the consequent intramolecular cyclopropanation. 6'-Demethyl quinine was found to be the efficient
