Stereocontrolled synthesis of quaternary cyclopropyl esters†
Abstract
Treatment of a variety of enantiopure terminal epoxides with the anion of a range of 2-substituted triethylphosphonoacetates leads to an array of quaternary
* Corresponding authors
a
Queen Mary University of London, School of Biological and Chemical Sciences, Mile End Road, London, UK
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c.bray@qmul.ac.uk
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Treatment of a variety of enantiopure terminal epoxides with the anion of a range of 2-substituted triethylphosphonoacetates leads to an array of quaternary
C. D. Bray and F. Minicone, Chem. Commun., 2010, 46, 5867 DOI: 10.1039/C0CC01333A
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