The title phosphonium ylides give an ylidene oxolactone under reductive conditions and are unreactive towards aldehydes, but are degraded by hydroxylamine to form the simpler acetic ester phosphonium ylides that do react with aldehydes in the normal manner.
AitkenR.A., HerionH., JanosiA., KarodiaN., RautS. V., SethS., ShannonI. J., and SmithF. C., J. Chem. Soc., Perkin Trans. 1, 1994, 2467.
6.
AitkenR.A., KarodiaN., and LightfootP., J. Chem. Soc., Perkin Trans. 2, 2000, 333.
7.
AitkenR.A., Al-AwadiN. A., BalkovichM. E., BestmannH. J., ClemO., GibsonS., GroßA., KumarA., and RöderT., Eur. J. Org. Chem., 2003, 840.
8.
AitkenR.A., and ThomasA. W., in Chemistry of the Functional Groups, Supplement A3, ed. PataiS., Wiley, Chichester, 1997, pp. 473–536.
9.
KeglevichGy., KörtvélyesiT., ForintosH., and LovasS., J. Chem. Soc., Perkin Trans. 2., 2002, 10, 1645.
10.
VedejsE., and MarthC. F., In Phosphorus-31 NMR Spectral Properties in Compound Characterization and Structural Analysis; QuinL.D., and VerkadeJ. G., Eds.; VHC, New York, 1994; Ch. 23, p. 297.
11.
UchiyamaT., FujimotoT., KakehiA., and YamamotoI., J. Chem. Soc., Perkin Trans. 1., 1999, 1577.