Journal
ORGANIC LETTERS
Volume 18, Issue 10, Pages 2491-2494Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01065
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Funding
- National Natural Science Foundation of China [21273026, 21572028]
- Fundamental Research Funds for the Central Universities [DUT15LK37]
- Outstanding Young Scholars Development Growth Plan of universities in Liaoning Province [LJQ2015027]
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A new halogenation method to construct halogen-substituted quinoline moieties is described. The Cu-catalyzed intramolecular aza-Diels-Alder reaction and halogenation reaction proceeded smoothly under mild conditions to produce the corresponding 7-chloro-6H-chromeno[4,3-b]quinolines and 7-chloro-6H-thiochromend[4,3-b]quinolines in satisfactory yields.
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