152126-74-4Relevant academic research and scientific papers
Pyrolysis of β,γ,β'-trioxo phosphorus ylides: Convenient synthesis of symmetrical and unsymmetrical diacylalkynes
Aitken,Herion,Janosi,Raut,Seth,Shannon,Smith
, p. 5621 - 5622 (1993)
Flash vacuum pyrolysis of a series of 1,2,4-trioxo-3-triphenylphosphoranylidene-butane derivatives, formed by acylation of β-oxo-phosphorus ylides with α-oxo-acid chlorides, results in extrusion of Ph3PO exclusively across the 2,3-position to give diacylalkynes.
Structure and photochemical behaviour of 3-azido-acrylophenones: A matrix isolation infrared spectroscopy study
Lopes, Susy,Nunes, Cláudio M.,Gómez-Zavaglia, Andrea,Pinho E Melo, Teresa M.V.D.,Fausto, Rui
experimental part, p. 7794 - 7804 (2011/10/12)
(Z)-3-Azido-3-methoxycarbonyl-2-chloro-acrylophenone (MACBP) has been synthesized, isolated in low temperature argon and xenon matrices and studied by FTIR spectroscopy, complemented by DFT(B3LYP)/6-311++G(d,p) calculations. The molecule was characterized both structurally and spectroscopically, and its photochemistry used to probe the mechanism of photo-induced conversion of 3-azido-acrylophenones into oxazoles. In situ UV irradiation (λ = 235 nm) of matrix-isolated MACBP yielded as primary photoproduct a 2H-azirine, which undergoes subsequent photoisomerization to methyl 4-chloro-5-phenyl-1,3-oxazole- 2-carboxylate. In a competitive process, a ketenimine is also formed upon photolysis of MACBP. The reported results indicate that this ketenimine must be formed from the starting 3-azido-acrylophenone via a Curtius type concerted rearrangement.
Flash Vacuum Pyrolysis of Stabilized Phosphorous Ylides. Part 5. Selective Extrusion of Ph3PO from β,γ,β'-Trioxo Ylides to give Doacylalkynes
Aitken, R. Alan,Herion, Hugues,Janosi, Amaya,Karodia, Nazira,Raut, Swati V.,et al.
, p. 2467 - 2472 (2007/10/02)
Sixteen examples of the previously unknown trioxo ylides 7 have been prepared by acylation of stabilized phosphorus ylides 8 with α-oxo acid chlorides 9.Extrusion of Ph3PO from these is readily achieved using FVP at 500 deg C in most cases, to afford the diacylalkynes 10 in moderate yield.Three examples failed to give the expected alkynes and the nature of the processes involved in these cases is certain.Fully assigned 13C NMR spectra are presented for the ylides and an unexpected pattern is observed in the value of JP-C for the three carbonyl carbons depending on the nature of the substituents present.There is some correlation between the value of 2JP-C for the central carbonyl carbon and the success of the pyrolysis although this is not complete.The method has been used to prepare a specifically 13C labelled acetylenic diester 14.
