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Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis.
Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N C; Cui, Jian-Fang.
Afiliação
  • Guo J; Department of Chemistry, Southern University of Science and Technology 1088 Xueyuan Blvd Shenzhen 518055 China cuijf@sustech.edu.cn.
  • Xiong WB; Department of Chemistry, Southern University of Science and Technology 1088 Xueyuan Blvd Shenzhen 518055 China cuijf@sustech.edu.cn.
  • Ma HR; Department of Chemistry, Southern University of Science and Technology 1088 Xueyuan Blvd Shenzhen 518055 China cuijf@sustech.edu.cn.
  • Fan L; School of Science and Engineering, The Chinese University of Hong Kong (Shenzhen) 2001 Longxiang Blvd Shenzhen 518172 China.
  • Zhou YY; Department of Chemistry, Southern University of Science and Technology 1088 Xueyuan Blvd Shenzhen 518055 China cuijf@sustech.edu.cn.
  • Wong HNC; Department of Chemistry, Southern University of Science and Technology 1088 Xueyuan Blvd Shenzhen 518055 China cuijf@sustech.edu.cn.
  • Cui JF; Department of Chemistry, Southern University of Science and Technology 1088 Xueyuan Blvd Shenzhen 518055 China cuijf@sustech.edu.cn.
Chem Sci ; 13(16): 4608-4615, 2022 Apr 20.
Article em En | MEDLINE | ID: mdl-35656141
ABSTRACT
We report herein a novel approach involving optical resolution of (±)-1,16-dihydroxytetraphenylene (DHTP) by chiral gold(iii) complexation. This method features several key advantages, i.e., recyclability of chiral resolution reagents, feasibility of scaling up to gram quantities, and operational simplicity. On the basis of this method, which led to optically pure DHTP, a library of 2,15-diaryl (S)-DHTPs and several (S)-DHTP-derived phosphoramidite ligands were synthesized. Finally, the superior performance of a (S)-DHTP phosphoramidite ligand was demonstrated by efficient iridium-catalyzed asymmetric allylic alkynylation reactions.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article