α-Fluorination of β-dicarbonyl compounds using p-iodotoluene difluoride under neutral conditions

スポンサーリンク

概要

• 論文の詳細を見る

• A selective introduction of a fluorine atom into the α-position of β-dicarbonyl compounds was achieved using p-iodotoluene difluoride. The reaction proceeded under mild conditions and monofluorination of β-ketoesters, ketoamides, and diketones selectively took place.

• Arkat-USAの論文

著者

• Hara Shoji

  Hokkaido Univ. Sapporo Jpn

• Yoshida Masanori

  Div. Of Chemical Process Engineering Graduate School Of Engineering Hokkaido Univ. 8 Kita 13-jo Nish

関連論文

• Stereoselective synthesis of fluoroalkenes via (Z)-2-fluoroalkenyliodonium salts
• Stereoselective synthesis of (Z)-β-fluoro-α,β-unsaturated esters from (Z)-2-fluoro-1-alkenyliodonium salts
• Fluorination of Ketones Using Iodotoluene Difluoride
• α-Fluorination of β-dicarbonyl compounds using p-iodotoluene difluoride under neutral conditions
• Direct Fluorination of Adamantanes with Iodine Pentafluoride

スポンサーリンク