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Original Articles

Unusual behavior of phosphonocyclopropyl sulfoxides

, &
Pages 180-181 | Received 17 Oct 2016, Accepted 17 Oct 2016, Published online: 24 Oct 2016
 

GRAPHICAL ABSTRACT

ABSTRACT

Synthesis of acylated phosphonocyclopropyl sulfoxide was performed in order to confirm some mechanistic aspects of 1,2 phosphoryl group migration. Reduction using phenylsilane in the KOH-catalyzed system was applied successfully for the conversion of carboalkoxy group to the corresponding alcohol. However, when both carboalkoxy and sulfinyl substituents were present at the same carbon atom, desulfinylation product was observed.

Funding

The authors acknowledge financial support through Grant DEC-2013/11/B/ST5/01589.

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