A multicomponent route to functionalized amides and oxazolidinones
McPherson, Christopher G. and Cooper, Alasdair K. and Bubliauskas, Andrius and Mulrainey, Paul and Jamieson, Craig and Watson, Allan J. B. (2017) A multicomponent route to functionalized amides and oxazolidinones. Organic Letters. ISSN 1523-7060 (https://doi.org/10.1021/acs.orglett.7b03470)
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Abstract
An organobase-mediated, multicomponent reaction of unactivated esters, epoxides, and amines is reported, furnishing functionalized amide derivatives. A wide range of substrates are tolerated under the reaction conditions, including chiral epoxides, which react with no erosion of enantiopurity. Facile modification of the method, through replacing the ester derivative with dimethyl carbonate, enables access to the corresponding oxazolidinone derivatives.
ORCID iDs
McPherson, Christopher G. ORCID: https://orcid.org/0000-0002-3082-0515, Cooper, Alasdair K., Bubliauskas, Andrius, Mulrainey, Paul, Jamieson, Craig ORCID: https://orcid.org/0000-0002-6567-8272 and Watson, Allan J. B.;-
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Item type: Article ID code: 62573 Dates: DateEvent1 December 2017Published1 December 2017AcceptedNotes: This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.7b03470. Subjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry
Strategic Research Themes > Health and WellbeingDepositing user: Pure Administrator Date deposited: 08 Dec 2017 11:08 Last modified: 17 Dec 2024 09:20 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/62573