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Synthesis and post-functionalization of alternate-linked-meta-para-[2 n .1 n ]thiacyclophanes.
De Leger, Wout; Adriaensen, Koen; Robeyns, Koen; Van Meervelt, Luc; Thomas, Joice; Meijers, Björn; Smet, Mario; Dehaen, Wim.
Afiliação
  • De Leger W; Molecular Design and Synthesis, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium.
  • Adriaensen K; Molecular Design and Synthesis, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium.
  • Robeyns K; Institute of Condensed Matter and Nanosciences, Université catholique de Louvain, Place Louis Pasteur 1, B-1348 Louvain-la-Neuve, Belgium.
  • Van Meervelt L; Biomolecular Architecture, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium.
  • Thomas J; Molecular Design and Synthesis, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium.
  • Meijers B; Laboratory of Nephrology, Department of Immunology and Microbiology, KU Leuven, Herestraat 49, B-3000 Leuven, Belgium.
  • Smet M; Department of Nephrology and Renal Transplantation, University Hospitals Leuven, Herestraat 49, B-3000 Leuven, Belgium.
  • Dehaen W; Molecular Design and Synthesis, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium.
Beilstein J Org Chem ; 14: 2190-2197, 2018.
Article em En | MEDLINE | ID: mdl-30202471
In recent decades, considerable research attention has been devoted to new synthetic procedures for thiacyclophanes. Thiacyclophanes are widely used as host molecules for the molecular recognition of organic compounds as well as metals. Herein, we report the selective and high-yielding synthesis of novel alternate-linked-meta-para-thiacyclophanes. These novel thiacyclophanes are selectively synthesized in high-yielding procedures. Furthermore, post-functionalization of the phenolic moieties was successfully performed. The 3D structure of the alternate-linked-meta-para-[22.12]thiacyclophane was further elucidated via X-ray crystallographic analysis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Beilstein J Org Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Beilstein J Org Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Bélgica