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Synthesis of Vinylindoles and Vinylpyrroles by the Peterson Olefination or by Use of the Nysted Reagent

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JOURNAL OF HETEROCYCLIC CHEMISTRY
卷 48, 期 2, 页码 381-388

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WILEY-BLACKWELL
DOI: 10.1002/jhet.313

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  1. Wayland E. Noland Research Fellowship Fund

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Vinylindoles and vinylpyrroles were prepared from their corresponding aldehydes or ketones using the Peterson olefination, or by use of the Nysted reagent, a commercially available gem-dimetallic compound. The two methods provide efficient and convenient access to these useful heterocyclic 1,3-diene systems.

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