1979
DOI: 10.1016/0040-4020(79)80109-x
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α-Halogenoketones—XI

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Cited by 22 publications
(2 citation statements)
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“…Numerous aurone syntheses were reported in the literature: the Wheeler aurone synthesis from chalcone dihalides, oxidative cyclization of 2‘-hydroxychalcones, and ring closure of o -hydroxyaryl phenylethynyl ketones . These methods give generally good stereoselectivity, but they usually cannot completely prevent the formation of flavones.…”
mentioning
confidence: 99%
“…Numerous aurone syntheses were reported in the literature: the Wheeler aurone synthesis from chalcone dihalides, oxidative cyclization of 2‘-hydroxychalcones, and ring closure of o -hydroxyaryl phenylethynyl ketones . These methods give generally good stereoselectivity, but they usually cannot completely prevent the formation of flavones.…”
mentioning
confidence: 99%
“…This easy three step sequence was reported for the construction of aurone skeletons [172], natural flavonoids. Aurones possess many biological properties [173][174][175][176][177], and due to this many groups were interested in the development of convenient synthetic pathways [178][179][180][181][182][183][184]. The best results were reported with goldcatalyzed oxycyclization and have advantages such as excellent selectivities, milder reaction conditions, and avoided the formation of byproducts like flavones [185].…”
Section: Gold Assisted Synthesismentioning
confidence: 99%