2005Organic & Biomolecular ChemistryRequires access

Deprotonation–electrophile trapping of terminal epoxides

David M. Hodgson, Eirene H. M. Kirton, Steven M. Miles, Stéphanie Norsikian, Nigel J. Reynolds, Steven J. Coote

Open publisher page 19 citations

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.

About this research paper

What this paper is about

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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OpenAlex reports 19 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available 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.

Key concepts: Deprotonation, Electrophile, Chemistry, Epoxide, Trapping, Diamine, Terminal (telecommunication), Stereochemistry

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