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Deaminative Arylation of Amino Acid-derived Pyridinium Salts.


ABSTRACT: A Suzuki-Miyaura cross-coupling of ?-pyridinium esters and arylboroxines has been developed. Combined with formation of the pyridinium salts from amino acid derivatives, this method enables amino acid derivatives to be efficiently transformed into ?-aryl esters and amides. Under the mild conditions, broad functional group tolerance on both the amino acid derivatives and the arylboroxine are observed, including protic functional groups. Mechanistic studies support an alkyl radical intermediate, similar to other cross-couplings of alkylpyridinium salts.

SUBMITTER: Hoerrner ME 

PROVIDER: S-EPMC6894616 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

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Deaminative Arylation of Amino Acid-derived Pyridinium Salts.

Hoerrner Megan E ME   Baker Kristen M KM   Basch Corey H CH   Bampo Earl M EM   Watson Mary P MP  

Organic letters 20190829 18


A Suzuki-Miyaura cross-coupling of α-pyridinium esters and arylboroxines has been developed. Combined with formation of the pyridinium salts from amino acid derivatives, this method enables amino acid derivatives to be efficiently transformed into α-aryl esters and amides. Under the mild conditions, broad functional group tolerance on both the amino acid derivatives and the arylboroxine are observed, including protic functional groups. Mechanistic studies support an alkyl radical intermediate, s  ...[more]

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