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Title: Harnessing Alkylpyridinium Salts as Electrophiles in Deaminative Alkyl-Alkyl Cross-Couplings. Author: Plunkett S, Basch CH, Santana SO, Watson MP. Journal: J Am Chem Soc; 2019 Feb 13; 141(6):2257-2262. PubMed ID: 30682254. Abstract: A Negishi cross-coupling of alkylpyridinium salts and alkylzinc halides has been developed. This is the first example of alkyl-alkyl bond formation via cross-coupling of an alkyl amine derivative with an unactivated alkyl group, and allows both primary and secondary alkylpyridinium salts to react with primary alkylzinc halides with high functional group tolerance. When combined with formation of the pyridinium salts from primary amines, this method enables the noncanonical transformation of NH2 groups into a wide range of alkyl substituents with broad functional group tolerance.[Abstract] [Full Text] [Related] [New Search]