Studies with enamines: Functionally substituted enamines as aldehyde equivalents in Gewald reactions

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Abstract

Several aryl and functionally substituted enamines reacted with ethyl cyanoacetate and elemental sulfur to form 2-aminothiophene-3-carboxylic acid derivatives that proved to be excellent precursors for a variety of thiophenes. ©ARKAT-USA, Inc.

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Al-Mousawi, S., Moustafa, M. S., & Elnagdi, M. H. (2008). Studies with enamines: Functionally substituted enamines as aldehyde equivalents in Gewald reactions. Arkivoc, 2008(10), 17–25. https://doi.org/10.3998/ark.5550190.0009.a03

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