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Rhodium-catalyzed homo-coupling reaction of aryl Grignard reagents and its application for the synthesis of an integrin inhibitor.

Kazuyuki SatoSatoki TeranishiAtsushi SakaueYukiko KaruoAtsushi TaruiKentaro KawaiHiroyuki TakedaTatsuo KinashiMasaaki Omote
Published in: Beilstein journal of organic chemistry (2024)
A novel Rh-catalyzed one-pot homo-coupling reaction of aryl Grignard reagents was achieved. The reaction with bromobenzenes having an electron-donating group or a halogen substituent gave the corresponding homo-coupling products in good yields, although the reaction using heterocyclic or aliphatic bromides scarcely proceeded. A Rh(III)-bis(aryl) complex, which might be formed from RhCl(PPh 3 ) 3 and the aryl Grignard reagents, plays an important role in giving the homo-coupling products in this reaction. Furthermore, we applied the reaction to the synthesis of a novel inhibitor for integrins which is critical for several diseases.
Keyphrases
  • electron transfer
  • room temperature
  • ionic liquid