145223-08-1Relevant articles and documents
X=Y-ZH systems as potential 1,3-dipoles. Part 50:1 phenylselenyl halide induced formation of cyclic nitrones from alkenyl oximes
Dondas, H.Ali,Grigg, Ronald,Hadjisoteriou, Maria,Markandu, Jasothara,Thomas, W.Anthony,Kennewell, Peter
, p. 10087 - 10096 (2000)
Oximes possessing γ- δ or ω-alkenyl substituents are cyclised by phenylselenyl bromide, or by phenylselenyl chloride and an appropriate silver salt to the corresponding cyclic nitrones; the seleno nitrones undergo facially specific cycloaddition reactions with N-methylmaleimide; bis(alk-γ,δ-enyl) ketones undergo regiospecific cyclisation and stereospecific intramolecular cycloaddition to furnish spirocyclic products. (C) 2000 Elsevier Science Ltd.
Phenylselenyl Halide Induced Formation of Cyclic Nitrones from Alkenyl Oximes
Grigg, Ronald,Hadjisoteriou, Maria,Kennewell, Peter,Markandu, Jasothara
, p. 1537 - 1538 (2007/10/02)
Oximes possessing alk-γ- or -δ-enyl substituents are cyclised by phenylselenyl bromide, or by phenylselenyl chloride and an appropriate silver salt, to the corresponding cyclic nitrones; the seleno nitrones undergo facially specific cycloadditions with N-methylmaleimide, bis(alk-γ,δ-enyl) and bis(alk-δ,δ-enyl) ketones undergo regiospecific cyclisation and stereospecific cycloaddition to furnish spirocyclic products.