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- W4383313102 endingPage "10170" @default.
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- W4383313102 abstract "A convenient method for the synthesis of indoles has been developed by the sequential orchestration of the cross-coupling reaction of o-haloaniline and PIFA oxidation of the resulting 2-alkenylanilines. A highlight of this two-step indole synthesis is a modular strategy which is applicable to both acyclic and cyclic starting materials. Particularly noteworthy is the regiochemistry that is complementary to the Fischer indole synthesis and related variants. Direct preparation of N–H indoles with no N-protecting group is also advantageous." @default.
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- W4383313102 date "2023-07-06" @default.
- W4383313102 modified "2023-09-24" @default.
- W4383313102 title "Synthesis of Indoles from <i>o</i>-Haloanilines" @default.
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- W4383313102 doi "https://doi.org/10.1021/acs.joc.3c01047" @default.
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