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. © 2009 HeteroCorporation.
CITATION STYLE
Noland, W. E., Etienne, C. L., & Lanzatella, N. P. (2011). Synthesis of vinylindoles and vinylpyrroles by the Peterson olefination or by use of the Nysted reagent. Journal of Heterocyclic Chemistry, 48(2), 381–388. https://doi.org/10.1002/jhet.313
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