Extension of the Criegee Rearrangement: Synthesis of Enol Ethers from Secondary Allylic Hydroperoxides

DOI: 10.1021/jo00097a006

Source and publish data:

Journal of Organic Chemistry p. 5125 - 5127 (1994)

Update date:2022-08-03

Topics:

Authors:

Goodman, Richard M.

Kishi, Yoshito

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Article abstract of DOI:10.1021/jo00097a006

The Criegee rearrangement has been extended to secondary allylic hydroperoxides, allowing for the selective synthesis of cyclic and acyclic enol ethers; the effect of base and electrophilic agent was studied.

Full text of DOI:10.1021/jo00097a006

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