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- W3021573089 endingPage "138" @default.
- W3021573089 startingPage "107" @default.
- W3021573089 abstract "The direct addition of an organocopper or cuprate reagent to a carbon–heteroatom multiple bond might rightfully be considered the forgotten son of transition metal based carbon–carbon bond formation. Indeed, although organocopper reagents are potent Michael donors, their well-recognized hesitation towards competing 1,2-addition may represent their most salient feature. Still, in most circumstances, while many substitution reactions1 (e.g. with a primary iodide) and especially 1,4-additions2 (e.g. with α,β-unsaturated ketones) tend to be far more rapid processes, the appropriately designed substrate can often benefit considerably from a copper reagent mediated 1,2-addition, not only in terms of yield but especially with regard to diastereoselectivity." @default.
- W3021573089 created "2020-05-13" @default.
- W3021573089 creator A5089736452 @default.
- W3021573089 date "1991-01-01" @default.
- W3021573089 modified "2023-09-23" @default.
- W3021573089 title "Organocopper Reagents" @default.
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