Direct Addition of Grignard Reagents to Aliphatic Carboxylic Acids Enabled by Bulky turbo ‐Organomagnesium Anilides
Autor: | Kilian Colas, A. Catarina V. D. Santos, Stefanie V. Kohlhepp, Abraham Mendoza |
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Rok vydání: | 2022 |
Předmět: | |
Zdroj: | Chem. Eur. J. |
ISSN: | 1521-3765 0947-6539 |
DOI: | 10.1002/chem.202200295 |
Popis: | The synthesis of ketones through addition of organometallic reagents to aliphatic carboxylic acids is a straightforward strategy that is limited to organolithium reagents. More desirable Grignard reagents can be activated and controlled with a bulky aniline-derived turbo-Hauser base. This operationally simple procedure allows the straightforward preparation of a variety of aliphatic and perfluoroalkyl ketones alike from functionalized alkyl, aryl and heteroaryl Grignard reagents. |
Databáze: | OpenAIRE |
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