Journal
SYNTHESIS-STUTTGART
Volume -, Issue 3, Pages 463-468Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0030-1258380
Keywords
aza-Diels-Alder reaction; dihydro-3H-chromeno[3,4-b][4,7]phenanthrolin-3-one; chromeno[4,3-b]pyrano[3,2-f]quinolin-3(13H)-one; Lewis acid catalysis; annulated quinoline
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Funding
- CSIR (New Delhi)
- DST (New Delhi)
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Dihydro-3H-chromeno[3,4-b][4,7]phenanthrolin-3-one and chromeno[4,3-b]pyrano[3,2-f]quinolin-3(13H)-one derivatives have been synthesized by aza-Diels-Alder reaction of O-propargylated salicylaldehyde with 6-aminoquinolone and 6-aminocoumarin respectively. The reaction occurs in a single-step operation and provides potentially bioactive polycyclic heterocycles in high yields.
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