Beilstein Journal of Organic Chemistry (Apr 2020)

Preparation of 2-phospholene oxides by the isomerization of 3-phospholene oxides

  • Péter Bagi,
  • Réka Herbay,
  • Nikolett Péczka,
  • Zoltán Mucsi,
  • István Timári,
  • and György Keglevich

DOI
https://doi.org/10.3762/bjoc.16.75
Journal volume & issue
Vol. 16, no. 1
pp. 818 – 832

Abstract

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A series of 1-substituted-3-methyl-2-phospholene oxides was prepared from the corresponding 3-phospholene oxides by double bond rearrangement. The 2-phospholene oxides could be obtained by heating the 3-phospholene oxides in methanesulfonic acid, or via the formation of cyclic chlorophosphonium salts. Whereas mixtures of the 2- and 3-phospholene oxides formed, when the isomerization of 3-phospholene oxides was attempted under thermal conditions, or in the presence of a base. The mechanisms of the various double bond migration pathways were elucidated by quantum chemical calculations.

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