Synthesis of 1-oxacephams via improved cyclization of N-substituted-4- formyloxyazetidin-2-ones

DOI: 10.1016/S0040-4039(98)01841-3

Source and publish data:

Tetrahedron Letters p. 8349 - 8352 (1998)

Update date:2022-07-30

Topics:: Authors:

Kaluza, Zbigniew

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Article abstract of DOI:10.1016/S0040-4039(98)01841-3

The Lewis acid promoted cyclisation of N-substituted-4- formyloxyazetidin-2-ones, easily available from 4-vinyloxyazetidin-2-one is described. The efficiency of the ring closure reaction, to give 1-oxacephams, depends on the oxygen protected-activated group and the Lewis acid.

Full text of DOI:10.1016/S0040-4039(98)01841-3

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Article Doi

Synthesis of 1-oxacephams via improved cyclization of N-substituted-4- formyloxyazetidin-2-ones

DOI: 10.1016/S0040-4039(98)01841-3

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(98)01841-3

Full text of DOI:10.1016/S0040-4039(98)01841-3

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