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CuI/Oxalic Diamide-Catalyzed Cross-Coupling of Thiols with Aryl Bromides and Chlorides.
Chen, Chia-Wei; Chen, Yi-Ling; Reddy, Daggula Mallikarjuna; Du, Kai; Li, Chao-En; Shih, Bo-Hao; Xue, Yung-Jing; Lee, Chin-Fa.
Afiliación
  • Chen CW; Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, 402, R.O.C.
  • Chen YL; Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, 402, R.O.C.
  • Reddy DM; Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, 402, R.O.C.
  • Du K; Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, 402, R.O.C.
  • Li CE; Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, 402, R.O.C.
  • Shih BH; Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, 402, R.O.C.
  • Xue YJ; Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, 402, R.O.C.
  • Lee CF; Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, 402, R.O.C.
Chemistry ; 23(42): 10087-10091, 2017 Jul 26.
Article en En | MEDLINE | ID: mdl-28510281
ABSTRACT
We report a general copper-catalyzed cross-coupling of thiols with aryl halides by using N-aryl-N'-alkyl oxalic diamide (L3) or N,N'-dialkyl oxalic diamide (L5) as the ligand. Both aryl and alkyl thiols can be coupled with unactivated aryl bromides and chlorides to give the desired products in good yields. Furthermore, this system features a broad substrate scope and good tolerance of functional groups. Importantly, the oxalic diamides are stable and can be prepared easily from commercially available and cheap starting materials.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2017 Tipo del documento: Article