Deprotonation–electrophile trapping of terminal epoxides
David M. Hodgson, Eirene H. M. Kirton, Steven M. Miles, Stéphanie Norsikian, Nigel J. Reynolds, Steven J. Coote
Abstract
David M. Hodgson, Eirene H. M. Kirton, Steven M. Miles, Stéphanie Norsikian, Nigel J. Reynolds, Steven J. Coote
Abstract
Organolithium-induced deprotonation of terminal epoxides in the presence of appropriate diamine ligands allows trapping with a range of electrophiles, yielding functionalised di- and tri-substituted epoxides in good yields and with control of stereochemistry at the epoxide.
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Organolithium-induced deprotonation of terminal epoxides in the presence of appropriate diamine ligands allows trapping with a range of electrophiles, yielding functionalised di- and tri-substituted epoxides in good yields and with control of stereochemistry at the epoxide.
Key concepts: Deprotonation, Electrophile, Chemistry, Epoxide, Trapping, Diamine, Terminal (telecommunication), Stereochemistry