Dimethyldioxirane epoxidation of 6,6-disubstituted fulvenes

DOI: 10.1016/S0040-4039(00)93578-0

Source and publish data:

Tetrahedron Letters p. 6697 - 6700 (1991)

Update date:2022-08-03

Topics:

Authors:

Adam Adam

Hadjiarapoglou

Meffert Meffert

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Article abstract of DOI:10.1016/S0040-4039(00)93578-0

The endocyclic bis-epoxides of various pentafulvenes were readily prepared by epoxidation with excess dimethyldioxirane; stoichiometric epoxidation yielded mixtures of the bis-epoxides and the labile monoepoxides, but no exocyclic epoxides were observed.

Full text of DOI:10.1016/S0040-4039(00)93578-0

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