Journal
GREEN CHEMISTRY
Volume 12, Issue 11, Pages 2003-2011Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0gc00265h
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Funding
- Ministry of Knowledge Economy (MKE) [RTI04-01-04]
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In water medium, environmentally benign, facile, and efficient synthesis of pyrans was achieved in good yields by the reactions of a variety of cyclic 1,3-dicarbonyls with several alpha, beta-unsaturated aldehydes. The key strategy was a formal [3 + 3] cycloaddition by domino Knoevenagel/6 pi-electrocyclization. This methodology was applied to the synthesis of biologically interesting pyranocoumarin, pyranoquinolinone, and pyranonaphthoquinone derivatives along with selected natural and non-natural products.
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