Abstract
In the presence of triethylamine as catalyst, the one-pot four-component reactions of arylamines, methyl propiolate, isatin and malononitrile afforded the functionalized spiro[indoline-3,4'-pyridine] derivatives in good yields. Similar reactions with ethyl cyanoacetate successfully afforded the functionalized spiro[indoline-3,4'-pyridines] and spiro[indoline-3,4'- pyridinones] as the main products according to the structures of the arylamines and other primary amines. © 2013 Zhang et al.
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CITATION STYLE
Zhang, L. J., Wu, Q., Sun, J., & Yan, C. G. (2013). Synthesis of functionalized spiro[indoline-3,4’-pyridines] and spiro[indoline-3,4’-pyridinones] via one-pot four-component reactions. Beilstein Journal of Organic Chemistry, 9, 846–851. https://doi.org/10.3762/bjoc.9.97
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