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Palladium-Catalyzed Double N-Arylation to Access Unsymmetric N,N'-Bicarbazole Scaffolds.
Zhang, Huan; Ding, Yi; Zhang, Mei-Ru; Lu, Chuan-Jun; Feng, Jia; Liu, Ren-Rong.
Afiliación
  • Zhang H; College of Chemistry and Chemical Engineering, Qingdao University, NingXia Road #308, Qingdao, Shandong 266071, China.
  • Ding Y; Shandong Institute for Food and Drug Control, Jinan, Shandong 250101, P. R. China.
  • Zhang MR; College of Chemistry and Chemical Engineering, Qingdao University, NingXia Road #308, Qingdao, Shandong 266071, China.
  • Lu CJ; College of Chemistry and Chemical Engineering, Qingdao University, NingXia Road #308, Qingdao, Shandong 266071, China.
  • Feng J; College of Chemistry and Chemical Engineering, Qingdao University, NingXia Road #308, Qingdao, Shandong 266071, China.
  • Liu RR; College of Chemistry and Chemical Engineering, Qingdao University, NingXia Road #308, Qingdao, Shandong 266071, China.
J Org Chem ; 88(14): 10242-10251, 2023 Jul 21.
Article en En | MEDLINE | ID: mdl-37432657
ABSTRACT
Herein, the palladium-catalyzed double C-N coupling of 9H-carbazol-9-amines and 2,2'-dibromo-1,1'-biphenyl is reported. This protocol offers access to N,N'-bicarbazole scaffolds, which have frequently been used as linkers in the construction of functional covalent organic frameworks (COFs). A variety of substituted N,N'-bicarbazoles were synthesized in moderate to high yields based on this chemistry, and the potential application of this method was showcased by the synthesis of COF monomers like tetrabromide 4 and tetraalkynylate 5.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2023 Tipo del documento: Article País de afiliación: China