The unusual Baeyer-Villiger rearrangement of β-lactam aldehdyes: Totally stereoselective entry to cis-3-substituted 4-formyloxy-2-azetidinones

DOI: 10.1016/0040-4039(95)00492-U

Source and publish data:

Tetrahedron Letters p. 3401 - 3404 (1995)

Update date:2022-08-02

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Authors:

Alcaide Alcaide

Aly Aly

Sierra Sierra

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Article abstract of DOI:10.1016/0040-4039(95)00492-U

Baeyer-Villiger oxidation of 4-formyl-β-lactams 1 with m-chloroperbenzoic acid in dichloromethane at room temperature is shown to be a convenient method for the preparation of 4-formyloxy-β-lactams 2. Some reactions of novel compounds 2 are also described

Full text of DOI:10.1016/0040-4039(95)00492-U

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Product name:2-Azetidinone, 4-(formyloxy)-1-(4-methoxyphenyl)-3,3-dimethyl-

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