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- W1541008022 endingPage "8125" @default.
- W1541008022 startingPage "8119" @default.
- W1541008022 abstract "The direct arylation of benzo[b]furan, benzo[b]thiophene, and indole has been studied by using aromatic bromides as the aryl source. The protocol employing common reagents and a Pd catalyst has led to the regioselective arylation of these heterocycles at the 2-position. A range of functional groups were tolerated, providing quick access to a variety of arylated benzo-fused heterocycles that would be accessible more elaborately using classical synthetic strategies. This is the first systematic study of the direct arylation of benzo[b]furan." @default.
- W1541008022 created "2016-06-24" @default.
- W1541008022 creator A5019600527 @default.
- W1541008022 creator A5049752995 @default.
- W1541008022 creator A5066135839 @default.
- W1541008022 creator A5077254155 @default.
- W1541008022 creator A5085200056 @default.
- W1541008022 date "2014-11-17" @default.
- W1541008022 modified "2023-10-08" @default.
- W1541008022 title "Direct Arylation of Benzo[<i>b</i>]furan and Other Benzo-Fused Heterocycles" @default.
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