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- W2016050721 endingPage "9714" @default.
- W2016050721 startingPage "9689" @default.
- W2016050721 abstract "The scope of palladium-catalyzed, auxiliary-assisted direct arylation and alkylation of sp2 and sp3 C–H bonds of amine and carboxylic acid derivatives has been investigated. The method employs a palladium acetate catalyst, substrate, aryl, alkyl, benzyl, or allyl halide, and inorganic base in tert-amyl alcohol or water solvent at 100–140 °C. Aryl and alkyl iodides as well as benzyl and allyl bromides are competent reagents in this transformation. The picolinic acid auxiliary is used for amine γ-functionalization, and the 8-aminoquinoline auxiliary is used for carboxylic acid β-functionalization. Some optimization of base, additives, and solvent is required for achieving best results." @default.
- W2016050721 created "2016-06-24" @default.
- W2016050721 creator A5008501544 @default.
- W2016050721 creator A5049326154 @default.
- W2016050721 creator A5052846414 @default.
- W2016050721 creator A5073541770 @default.
- W2016050721 date "2013-09-19" @default.
- W2016050721 modified "2023-10-11" @default.
- W2016050721 title "Scope and Limitations of Auxiliary-Assisted, Palladium-Catalyzed Arylation and Alkylation of sp<sup>2</sup> and sp<sup>3</sup> C–H Bonds" @default.
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