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Oxygen- and Nitrogen-Embedded Zigzag Hydrocarbon Belts.
Tan, Mei-Ling; Guo, Qing-Hui; Wang, Xue-Yuan; Shi, Tan-Hao; Zhang, Qian; Hou, Sheng-Kai; Tong, Shuo; You, Jingsong; Wang, Mei-Xiang.
Afiliação
  • Tan ML; Key Laboratory of Green Chemistry and Technology (MOE), College of Chemistry, Sichuan University, Chengdu, 610064, China.
  • Guo QH; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (MOE), Department of Chemistry, Tsinghua University, Beijing, 100084, China.
  • Wang XY; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (MOE), Department of Chemistry, Tsinghua University, Beijing, 100084, China.
  • Shi TH; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (MOE), Department of Chemistry, Tsinghua University, Beijing, 100084, China.
  • Zhang Q; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (MOE), Department of Chemistry, Tsinghua University, Beijing, 100084, China.
  • Hou SK; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (MOE), Department of Chemistry, Tsinghua University, Beijing, 100084, China.
  • Tong S; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (MOE), Department of Chemistry, Tsinghua University, Beijing, 100084, China.
  • You J; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (MOE), Department of Chemistry, Tsinghua University, Beijing, 100084, China.
  • Wang MX; Key Laboratory of Green Chemistry and Technology (MOE), College of Chemistry, Sichuan University, Chengdu, 610064, China.
Angew Chem Int Ed Engl ; 59(52): 23649-23658, 2020 Dec 21.
Article em En | MEDLINE | ID: mdl-33047450
ABSTRACT
Despite the aesthetically appealing structures and tantalizing physical and chemical properties, zigzag hydrocarbon belts and their heteroatom-embedded analogues remain challenging synthetic targets. We report herein the synthesis of diverse O/N-doped zigzag hydrocarbon belts based on selective bridging of the fjords of resorcin[4]arene derivatives through intramolecular SN Ar and palladium-catalyzed intermolecular C-N bond formation reactions. Preorganized conformations of mono-macrocyclic, half-belt and quasi-belt compounds were revealed to facilitate cyclization reactions to construct heteroatom-linked octahydrobelt[8]arenes. The acquired products had strained square-prism-shaped belt structures in which all six-membered heterocyclic rings adopted an unusual boat conformation with equatorially configured alkyl groups. The unprecedented heteroatom-bearing belts also exhibited different photophysical and redox properties to those of octahydrobelt[8]arene analogues.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article