Journal of the Chemical Society. Perkin transactions I p. 2467 - 2472 (1994)
Update date:2022-08-04
Topics:
Aitken, R. Alan
Herion, Hugues
Janosi, Amaya
Karodia, Nazira
Raut, Swati V.
et al.
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.
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