Functionalization of 7-Azaindole

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概要

• 論文の詳細を見る

• Functionalization of 7-azaindole utilizing Reissert-Henze type reaction was studied. It was found that the direct halogenation, cyanation, and thiocyanation of 7-azaindole proceeded regioselectively. In chlorination of 7-azaindole, the regioselectivity was controlled by chlorination reagents as well as acylation reagents. These functional groups could be chemically modified to useful substituents.

• 近畿大学の論文
• 1998-02-28

著者

• Ohshiro Yoshiki

  近畿大学理工学総合研究所

• Kikuta Hiroshige

  近畿大学理工学総合研究所

関連論文

• Resonance Structure of Azaindoles
• Activities of 7-Azaindole Derivatives as Agricultural Fungicides
• Functionalization of 7-Azaindole
• Functionalization of Pyridines via Reissert-Henze Reaction
• Characteristic Reaction Mode of Cofactor PQQ toward Nucleophiles

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