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Royal Society of Chemistry, Organic and Biomolecular Chemistry, 44(14), p. 10427-10436

DOI: 10.1039/c6ob01989g

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An MEDT study of the carbenoid-type [3 + 2] cycloaddition reactions of nitrile ylides with electron-deficient chiral oxazolidinones

Journal article published in 2016 by Luis R. Domingo ORCID, Mar Ríos-Gutiérrez, Patricia Pérez ORCID
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

A combination of the bonding evolution theory and non-covalent interactions analyses of TSs makes it possible to characterise both the carbenoid-type 32CA reaction between a NY and a chiral oxazolidinone, and the diastereoselectivity experimentally observed.