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A 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)-catalyzed cascade annulation reaction between -quinamines and 3-formylchromones was developed, affording a series of benzopyrone-fused hydrobenzo[,]indoles in moderate to high yields with excellent diastereoselectivity. This cascade reaction is efficient since two new rings as well as one C-N, one C═C, and two C-C bonds are created in a single step. The scale-up synthesis and versatile transformations of the products further demonstrated the practicality and utility of this approach.
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http://dx.doi.org/10.1021/acs.orglett.4c02591 | DOI Listing |
Org Lett
August 2024
State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang 550014, People's Republic of China.
A 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)-catalyzed cascade annulation reaction between -quinamines and 3-formylchromones was developed, affording a series of benzopyrone-fused hydrobenzo[,]indoles in moderate to high yields with excellent diastereoselectivity.
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