193155-20-3Relevant academic research and scientific papers
Synthesis and pyrolytic and kinetic behaviour of β,δ′-dioxo-stabilised phosphorus ylides: Convenient preparation of γ,δ-alkynyl ketones and 2,3-functionalised butadienes
Aitken, R. Alan,Al-Awadi, Nouria A.,Balkovich, Mark E.,Bestmann, Hans Juergen,Clem, Oliver,Gibson, Scott,Gross, Andreas,Kumar, Ajith,Roeder, Thomas
, p. 840 - 847 (2003)
Both ketone- and ester-stabilised phosphorus ylides undergo Michael addition to vinyl ketones to give the β,δ′-dioxo ylides 3 and 5, respectively, although in the latter case careful temperature control is required to avoid an undesired side-reaction. Under conditions of flash vacuum pyrolysis at 650 °C the ylides 3 generally undergo Ph3PO extrusion to afford the γ,δ-alkynyl ketones 14, although these are found to partly undergo a secondary fragmentation. In contrast, the ylides 5 react under the same conditions to give the synthetically useful 1,3-dienes 20 by way of cyclobutenes. Rate constants for the reaction of selected ylides 3 and 5 are reported. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
Reaction of vinylketones with stabilized phosphoniumylids
Bestmann, Hans Juergen,Gross, Andreas
, p. 4765 - 4768 (2007/10/03)
Acylphosphoniumylids 1 react with vinylketones 2 under formation of 1-acyl-4-oxoylids 3. In the reaction of carboalkoxyetriphenylphosphoranes 4 with 2 two reaction pathways occur. In polar solvents again a Michael-addition gives the phosphoranes 6, wherea
