Answers are grounded in this paper and cite their sources.
Two as yet unknown cyclopentene‐triols have been prepared. The replacement of the halogen of cyclopentene derivatives brominated in the allylic position has been investigated. In the presence of dimethyl sulfoxide and sodium hydrogen carbonate, the bromine of some of the above mentioned allylic derivatives or the tosyloxy group of a dibenzoyloxy‐monotosyloxy‐cyclopentane derivative is replaced by a hydroxyl group without formation of any keto compound. The mechanism of action of the substitution agents is discussed.
No takes yet. Share an insight, caveat, or question.
Wolczunowicz et al. (1970) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: