Synthesis of 2,5-dihydrofurans via alkylidene carbene insertion reactions

DOI: 10.1016/S0040-4039(98)00998-8

Source and publish data:

Tetrahedron Letters p. 5273 - 5276 (1998)

Update date:2022-08-02

Topics:

Authors:

Walker, Louise F.

Connolly, Stephen

Wills, Martin

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Article abstract of DOI:10.1016/S0040-4039(98)00998-8

The insertion of vinylidene carbenes into C-H bonds is an efficient method for the synthesis of 2,5-dihydrofurans. The methodology provides a convenient entry to the core structure of squalestatin/zaragozic acid natural products.

Full text of DOI:10.1016/S0040-4039(98)00998-8

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