Palladium-Catalyzed Allylation of Acidic and Less Nucleophilic Anilines Using Allylic Alcohols Directly

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概要

• 論文の詳細を見る

• The direct activation of C-O bonds in allylic alcohols by palladium complexes has been accelerated by carrying out the reactions in the presence of titanium (IV) isoproxide and 4Å molecular sieves. The acidic and less nucleophilic anilines such as diphenylamine, phenothiazine, 4-cyanoaniline, and nitroanilines are efficiently allylated under palladium catalysis using allylic alcohols as allylating reagents.

• 公益社団法人日本薬学会の論文
• 2005-10-01

著者

• Gan Kim

  Graduate Institute Of Pharmaceutical Sciences Kaohsiung Medical University

• HSU Yi

  Graduate Institute of Pharmaceutical Sciences, Kaohsiung Medical University

• YANG Shyh

  Graduate Institute of Pharmaceutical Sciences, Kaohsiung Medical University

• Hsu Yi

  Graduate Institute Of Pharmaceutical Sciences Kaohsiung Medical University

• Yang Shyh

  Graduate Institute Of Pharmaceutical Sciences Kaohsiung Medical University

• Gan Kim-Hong

  Graduate Institute of Pharmaceutical Sciences, Kaohsiung Medical University

• Hsu Yi-Chun

  Graduate Institute of Pharmaceutical Sciences, Kaohsiung Medical University

• Yang Shyh-Chyun

  Graduate Institute of Pharmaceutical Sciences, Kaohsiung Medical University

関連論文

• Palladium-Catalyzed Allylation of Acidic and Less Nucleophilic Anilines Using Allylic Alcohols Directly

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