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In Search of Wasserman's Catenane.
Baluna, Andrei S; Galan, Albano; Leigh, David A; Smith, Gareth D; Spence, Justin T J; Tetlow, Daniel J; Vitorica-Yrezabal, Iñigo J; Zhang, Min.
Afiliação
  • Baluna AS; Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
  • Galan A; Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
  • Leigh DA; Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
  • Smith GD; School of Chemistry and Molecular Engineering, East China Normal University, 200062 Shanghai, China.
  • Spence JTJ; Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
  • Tetlow DJ; Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
  • Vitorica-Yrezabal IJ; Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
  • Zhang M; Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
J Am Chem Soc ; 145(17): 9825-9833, 2023 May 03.
Article em En | MEDLINE | ID: mdl-37096971
We repeat the earliest claimed [2]catenane synthesis, reported by Wasserman over 60 years ago, in order to ascertain whether or not a nontemplate, statistical synthesis by acyloin macrocyclization does indeed form mechanically interlocked rings. The lack of direct experimental evidence for Wasserman's catenane has led to it being described as a "prophetic compound", a technical term used in patents for claimed molecules that have not yet been synthesized. Contemporary synthetic methods were used to reconstruct Wasserman's deuterium-labeled macrocycle and other building blocks on the 10-100 g reaction scale necessary to generate, in principle, ∼1 mg of catenane. Modern spectrometric and spectroscopic tools and chemical techniques (including tandem mass spectrometry, deuterium nuclear magnetic resonance (NMR) spectroscopy, and fluorescent tag labeling) were brought to bear in an effort to detect, isolate, and prove the structure of a putative [2]catenane consisting of a 34-membered cyclic hydrocarbon mechanically linked with a 34-membered cyclic α-hydroxyketone.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article