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Merging photoredox and nickel catalysis: decarboxylative cross-coupling of carboxylic acids with vinyl halides.


ABSTRACT: Decarboxylative cross-coupling of alkyl carboxylic acids with vinyl halides has been accomplished through the synergistic merger of photoredox and nickel catalysis. This new methodology has been successfully applied to a variety of ?-oxy and ?-amino acids, as well as simple hydrocarbon-substituted acids. Diverse vinyl iodides and bromides give rise to vinylation products in high efficiency under mild, operationally simple reaction conditions.

SUBMITTER: Noble A 

PROVIDER: S-EPMC4308738 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

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Merging photoredox and nickel catalysis: decarboxylative cross-coupling of carboxylic acids with vinyl halides.

Noble Adam A   McCarver Stefan J SJ   MacMillan David W C DW  

Journal of the American Chemical Society 20150112 2


Decarboxylative cross-coupling of alkyl carboxylic acids with vinyl halides has been accomplished through the synergistic merger of photoredox and nickel catalysis. This new methodology has been successfully applied to a variety of α-oxy and α-amino acids, as well as simple hydrocarbon-substituted acids. Diverse vinyl iodides and bromides give rise to vinylation products in high efficiency under mild, operationally simple reaction conditions. ...[more]

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