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Sodium methyl carbonate as an effective C1 synthon. Synthesis of carboxylic acids, benzophenones, and unsymmetrical ketones

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dc.contributor.authorHurst, Timothy E.
dc.contributor.authorDeichert, Julie A.
dc.contributor.authorKapeniak, Lucas
dc.contributor.authorLee, Roland
dc.contributor.authorHarris, Jesse
dc.contributor.authorJessop, Philip G.
dc.contributor.authorSnieckus, Victor
dc.date.accessioned2020-10-16
dc.date.accessioned2022-05-31T01:15:55Z
dc.date.available2022-05-31T01:15:55Z
dc.date.issued2019
dc.description.abstractReported is the synthesis of carboxylic acids, symmetrical ketones, and unsymmetrical ketones with selectivity achieved by exploiting the differential reactivity of sodium methyl carbonate with Grignard and organolithium reagents.
dc.description.urihttps://library.macewan.ca/full-record/edswsc/000471212100002
dc.identifier.citationTimothy E. Hurst, Julie A. Deichert, Lucas Kapeniak, Roland Lee, Jesse Harris, Philip G. Jessop and Victor Snieckus. Sodium Methyl Carbonate as an Effective C1 Synthon. Synthesis of Carboxylic Acids, Benzophenones, and Unsymmetrical Ketones, Organic letters, (2019) 21, 11, 3882-3885
dc.identifier.doihttps://doi.org/10.1021/acs.orglett.9b00773
dc.identifier.urihttps://hdl.handle.net/20.500.14078/1940
dc.languageEnglish
dc.language.isoen
dc.rightsAll Rights Reserved
dc.subjectsodium methyl carbonate
dc.subjectsynthesis of symmetrical ketones
dc.subjectunsymmetrical ketones
dc.subjectGrignard reagents
dc.subjectorganolithium
dc.subjectC1 synthon
dc.subjectalkyl metal carbonates
dc.subjectcarboxylic acids
dc.subjectbenzophenones
dc.titleSodium methyl carbonate as an effective C1 synthon. Synthesis of carboxylic acids, benzophenones, and unsymmetrical ketonesen
dc.typeArticle

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