3-Trimethylsilyloxy-oxetanes via a highly selective Paterno-Buchi reaction

DOI: 10.1016/0040-4039(91)85033-2

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Tetrahedron Letters p. 7037 - 7038 (1991)

Update date:2022-08-03

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Bach

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Article abstract of DOI:10.1016/0040-4039(91)85033-2

Benzaldehyde reacts photochemically with various trimethylsilyl enol ethers to furnish 3-trimethylsilyloxy-oxetanes in moderate to fair fields. The photocycloaddition proceeds with excellent regio- and diastereoselectivity.

Full text of DOI:10.1016/0040-4039(91)85033-2

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Article Doi

3-Trimethylsilyloxy-oxetanes via a highly selective Paterno-Buchi reaction

DOI: 10.1016/0040-4039(91)85033-2

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(91)85033-2

Full text of DOI:10.1016/0040-4039(91)85033-2

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