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Manganese-Catalyzed Carboacylations of Alkenes with Alkyl Iodides.

ABSTRACT: A manganese-catalyzed carboacylation of alkenes with alkyl iodides and carbon monoxide is described. This carbonylative difunctionalization uses both primary and secondary alkyl iodides in reactions with a diverse array of cyclic and acyclic substrates. Examples of successful applications to the synthesis of five-, six-, and seven-membered rings are provided. The inexpensive, first-row catalytic system and mild reaction conditions are expected to facilitate applications in complex synthesis.

SUBMITTER: McMahon CM

PROVIDER: S-EPMC5359471 | biostudies-literature | 2016 Aug

REPOSITORIES: biostudies-literature

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Manganese-Catalyzed Carboacylations of Alkenes with Alkyl Iodides.

McMahon Caitlin M CM Renn Matthew S MS Alexanian Erik J EJ

Organic letters 20160809 16

A manganese-catalyzed carboacylation of alkenes with alkyl iodides and carbon monoxide is described. This carbonylative difunctionalization uses both primary and secondary alkyl iodides in reactions with a diverse array of cyclic and acyclic substrates. Examples of successful applications to the synthesis of five-, six-, and seven-membered rings are provided. The inexpensive, first-row catalytic system and mild reaction conditions are expected to facilitate applications in complex synthesis. ...[more]

PMID: 27505233

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