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Octopus[5]arene from Pagoda[5]arene by Macrocycle-to-Macrocycle Conversion.
Liu, Ningning; Han, Xiao-Ni; Ma, Hui; Guo, Wei-Chen; Han, Ying; Zhang, Chun; Zheng, Yan-Song; Chen, Chuan-Feng.
Afiliação
  • Liu N; College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Han XN; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
  • Ma H; College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Guo WC; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
  • Han Y; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
  • Zhang C; College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Zheng YS; School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Chen CF; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Org Lett ; 2024 Aug 19.
Article em En | MEDLINE | ID: mdl-39158085
ABSTRACT
Macrocycle-to-macrocycle conversion is an effective strategy to construct new macrocyclic arenes with specific structures. Herein, a new class of chiral macrocyclic arene, namely, octopus[5]arenes (Oc5s), cannot be synthesized by the direct approach from the corresponding chiral monomers but can be successfully achieved by a macrocycle-to-macrocycle conversion strategy utilizing racemic pagoda[5]arenes as the starting materials. It was found that enantiomeric Oc5s showed fixed conformations and stable chiral structures and exhibited significant chiral recognition toward chiral diamines.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA