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Domino C-C/C-O bond formation: palladium-catalyzed regioselective synthesis of 7-iodobenzo[b]furans using 1,2,3-triiodobenzenes and benzylketones.


ABSTRACT: A facile and efficient synthesis of 7-iodobenzo[b]furan derivatives via a highly regioselective tandem α-arylation/intramolecular O-arylation of 5-substituted-1,2,3-triiodobenzenes and benzylketones is described. Remarkably, the α-arylation coupling reactions initiate exclusively at the least sterically-hindered position of the triiodoarene, which results in a highly chemoselective transformation. The highest yields were observed in reactions between electron-poor 1,2,3-triiodoarenes and electron-rich benzylketones, yet the optimized reaction conditions were found to be tolerant to a wide range of different functional groups. This unprecedent synthesis of 7-iodobenzo[b]furans from 1,2,3-triiodobenzenes is scalable, general in scope, and provides easy access to valuable precursors for other chemical transformations.

SUBMITTER: Al-Zoubi RM 

PROVIDER: S-EPMC9040925 | biostudies-literature | 2021 Sep

REPOSITORIES: biostudies-literature

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Domino C-C/C-O bond formation: palladium-catalyzed regioselective synthesis of 7-iodobenzo[<i>b</i>]furans using 1,2,3-triiodobenzenes and benzylketones.

Al-Zoubi Raed M RM   Al-Jammal Walid K WK   Ferguson Michael J MJ   Murphy Graham K GK  

RSC advances 20210908 48


A facile and efficient synthesis of 7-iodobenzo[<i>b</i>]furan derivatives <i>via</i> a highly regioselective tandem α-arylation/intramolecular <i>O</i>-arylation of 5-substituted-1,2,3-triiodobenzenes and benzylketones is described. Remarkably, the α-arylation coupling reactions initiate exclusively at the least sterically-hindered position of the triiodoarene, which results in a highly chemoselective transformation. The highest yields were observed in reactions between electron-poor 1,2,3-trii  ...[more]

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