Oxidative rearrangement of 3-aryl-1H-benzo[f]chromenes into 2-aroyl-1,2-dihydronaphtho[2,1-b]furans

被引：0
|
作者：
Kirill S. Korzhenko
Dmitry V. Osipov
Vitaly А. Osyanin
Maxim R. Demidov
Yuri N. Klimochkin
机构：
[1] Samara State Technical University,
来源：
Chemistry of Heterocyclic Compounds | 2021年 / 57卷
关键词：
2-aroyl-1,2-dihydronaphtho[2,1-; ]furans; 3-aryl-1; -benzo[; ]chromenes; -bromosuccinimide; oxidative rearrangement; ring constriction;
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学科分类号：
摘要：
By the reaction of 3-aryl-1H-benzo[f]chromenes with N-bromosuccinimide in aqueous acetone, a series of 2-aroyl-1,2-dihydronaphtho-[2,1-b]furans unsubstituted at the C-1 position were obtained as a result of formal addition of hypobromous acid to the pyran fragment and intramolecular nucleophilic substitution. This reaction is a rare example of the ring constriction in 1H-benzo[f]chromene series.
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页码：599 / 601
页数：2
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