化学
弗里德尔-克拉夫茨反应
烷基化
甲烷
有机化学
立体化学
催化作用
作者
Chutima Kuhakarn,Nakin Surapanich,Siriporn Kamtonwong,Manat Pohmakotr,Vichai Reutrakul
标识
DOI:10.1002/ejoc.201100715
摘要
Abstract Bromodifluoro(phenylsulfanyl)methane undergoes a Friedel–Crafts‐type alkylation, through α‐fluorocarbocations, with activated aromatic compounds yielding thioesters and/or benzophenones. The methodology has been applied to the synthesis of naturally occurring xanthone derivatives.
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