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Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides.

ABSTRACT: A new approach for the synthesis of 1,4-dicarbonyl compounds is reported. Chemoselective activation of amide carbonyl functionality and subsequent umpolung via N-oxide addition generates an electrophilic enolonium species that can be coupled with a wide range of nucleophilic enolates. The method conveys broad functional group tolerance on both components, does not suffer from formation of homocoupling byproducts and avoids the use of transition metal catalysts.

SUBMITTER: Kaiser D

PROVIDER: S-EPMC5691317 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

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Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides.

Kaiser Daniel D Teskey Christopher J CJ Adler Pauline P Maulide Nuno N

Journal of the American Chemical Society 20171103 45

A new approach for the synthesis of 1,4-dicarbonyl compounds is reported. Chemoselective activation of amide carbonyl functionality and subsequent umpolung via N-oxide addition generates an electrophilic enolonium species that can be coupled with a wide range of nucleophilic enolates. The method conveys broad functional group tolerance on both components, does not suffer from formation of homocoupling byproducts and avoids the use of transition metal catalysts. ...[more]

PMID: 29099184

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