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- W3133169133 endingPage "9711" @default.
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- W3133169133 abstract "Abstract Direct oxidative C(sp)−H/C(sp 3 )−H cross‐coupling offers an ideal and environmentally benign protocol for C(sp)−C(sp 3 ) bond formations. As such, reactivity and site‐selectivity with respect to C(sp 3 )−H bond cleavage have remained a persistent challenge. Herein is reported a simple method for iron‐catalyzed/silver‐mediated tertiary alkylation of terminal alkynes with readily available and versatile 1,3‐dicarbonyl compounds. The reaction is suitable for an array of substrates and proceeds in a highly selective manner even employing alkanes containing other tertiary, benzylic, and C(sp 3 )−H bonds alpha to heteroatoms. Elaboration of the products enables the synthesis of a series of versatile building blocks. Control experiments implicate the in situ generation of a tertiary carbon‐centered radical species." @default.
- W3133169133 created "2021-03-01" @default.
- W3133169133 creator A5037064277 @default.
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- W3133169133 creator A5065070495 @default.
- W3133169133 creator A5087217572 @default.
- W3133169133 date "2021-03-12" @default.
- W3133169133 modified "2023-09-27" @default.
- W3133169133 title "Iron‐Catalyzed Tertiary Alkylation of Terminal Alkynes with 1,3‐Diesters via a Functionalized Alkyl Radical" @default.
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- W3133169133 doi "https://doi.org/10.1002/anie.202100641" @default.
- W3133169133 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33590589" @default.
- W3133169133 hasPublicationYear "2021" @default.