Gold-catalysed synthesis of phosphonate-substituted oxetan-3-ones – an easy access to highly strained HWE reagents

A convenient approach for the attainment of strained phosphonate-substituted oxetan-3-ones, starting from easy to synthesise alkynyl phosphonates, is presented. With the aid of a pyridine- N -oxide, in a gold-catalysed step an α-oxo carbene species is generated as a key intermediate. After formal OH...

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Veröffentlicht in:Organic Chemistry Frontiers 2021-12, Vol.9 (1), p.117-122
Hauptverfasser: Tahir, Shaista, Wunsch, Jonas F., Rudolph, Matthias, Rominger, Frank, Hashmi, A. Stephen K.
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Sprache:eng
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Zusammenfassung:A convenient approach for the attainment of strained phosphonate-substituted oxetan-3-ones, starting from easy to synthesise alkynyl phosphonates, is presented. With the aid of a pyridine- N -oxide, in a gold-catalysed step an α-oxo carbene species is generated as a key intermediate. After formal OH-insertion, synthetically useful HWE reagents can be attained. The synthetic utility of the obtained building blocks could be demonstrated, which yielded the 2-alkenyl oxetan-3-one scaffold in high yields after the HWE reaction.
ISSN:2052-4129
2052-4110
2052-4129
2052-4110
DOI:10.1039/D1QO01214B