Synthesis of functionalized indolizines by lewis acid-mediated cyclocondensation of 3-(Pyridin-2-yl)-propiolates with enones

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Abstract

Functionalized indolizines were prepared by Lewis acid-catalyzed cyclizations of 3-(pyridin-2-yl)-propiolates with enones. This new type of reaction provides a convenient and regioselective approach to ester-substituted indolizine derivatives which are not readily available by other methods. Based on density function theory (DFT) calculations, a mechanism of the reaction has been suggested. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Specowius, V., Bendrath, F., Winterberg, M., Ayub, K., & Langer, P. (2012). Synthesis of functionalized indolizines by lewis acid-mediated cyclocondensation of 3-(Pyridin-2-yl)-propiolates with enones. Advanced Synthesis and Catalysis, 354(6), 1163–1169. https://doi.org/10.1002/adsc.201100795

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