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Copper- and Palladium-Catalyzed Cross-Coupling Reactions for the Synthesis of N-Fused Benzo[4,5]imidazo[2,1-b]thiazole Derivatives via Substituted trans-1,2-Diiodoalkenes, 1H-Benzo[d]imidazole-2-thiols, and Halobenzenes.

Guodong ShenBingchuan YangXianqiang HuangYaxin HouHuan GaoJichun CuiChuansheng CuiTongxin Zhang
Published in: The Journal of organic chemistry (2017)
Two transition metal (Cu and Pd)-catalyzed C-S, C-N, and C-C bond cross-coupling reactions for the preparation of N-fused benzo[4,5]imidazo[2,1-b]thiazole derivatives were developed. A variety of 3-substituted and 2,3-disubstituted benzo[4,5]imidazo[2,1-b]thiazoles were efficiently and conveniently synthesized from the coupling reaction via trans-1,2-diiodoalkenes, 1H-benzo[d]imidazole-2-thiols, and halobenzenes in moderate to excellent yields.
Keyphrases
  • transition metal
  • molecular docking
  • room temperature
  • mass spectrometry
  • ionic liquid
  • molecular dynamics simulations
  • liquid chromatography
  • metal organic framework
  • solid phase extraction