Dimethyldioxirane epoxidation of 6,6-disubstituted fulvenes
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.
Adam,Hadjiarapoglou,Meffert
p. 6697 - 6700
(2007/10/02)
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