Tandem aldehyde-alkyne-amine coupling/cycloisomerization: A new synthesis of coumarins

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Abstract

Cu-catalyzed A3 coupling of ethoxyacetylene, pyrrolidine and salicylaldehydes led to a concomitant cycloisomerization followed by hydrolysis of the resultant vinyl ether to afford coumarins in a cascade process. The reaction proceeded through exclusive 6-endo-dig cyclization and is compatible with halo and keto groups giving coumarins in good to moderate yields. © 2013 Reddy et al.

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Reddy, M. S., Thirupathi, N., & Haribabu, M. (2013). Tandem aldehyde-alkyne-amine coupling/cycloisomerization: A new synthesis of coumarins. Beilstein Journal of Organic Chemistry, 9, 180–184. https://doi.org/10.3762/bjoc.9.21

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