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.
Author supplied keywords
Cite
CITATION STYLE
APA
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
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free