Abstract
The reactive 1:1 intermediate is trapped from reaction between alkyl isocyanides and activated acetylenic esters by di-(2-pyridyl) ketone or 2-pyridinecarboxaldehyde. An effective and one-pot route is presented to synthesize novel iminolactones and 2-aminofurans. ©ARKAT USA, Inc.
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Hazeri, N., Maghsoodlou, M. T., Habibi-Khorassani, S. M., Marandi, G., Khandan-Barani, K., Ziyaadini, M., & Aminkhani, A. (2007). Synthesis of novel 2-pyridyl- substituted 2,5-dihydro-2-imino- and 2-amino- furan derivatives via a three component condensation of alkyl isocyanides and acetylenic esters with di-(2-pyridyl) ketone or 2-pyridinecarboxaldehyde. Arkivoc, 2007(1), 173–179. https://doi.org/10.3998/ark.5550190.0008.119
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