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A unified "top-down" approach for the synthesis of diverse lead-like molecular scaffolds.
Townley, Chloe; McMurray, Lindsay; Marsden, Stephen P; Nelson, Adam.
Afiliação
  • Townley C; School of Chemistry, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.
  • McMurray L; Oncology R&D, AstraZeneca, Cambridge CB4 0WG, UK.
  • Marsden SP; School of Chemistry, University of Leeds, Leeds LS2 9JT, UK. Electronic address: s.p.marsden@leeds.ac.uk.
  • Nelson A; School of Chemistry, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK. Electronic address: a.s.nelson@leeds.ac.uk.
Bioorg Med Chem Lett ; 62: 128631, 2022 04 15.
Article em En | MEDLINE | ID: mdl-35181466
A "top-down" synthetic approach enabled the step-efficient synthesis of 21 diverse novel molecular scaffolds. The scaffolds were derived from four complex intermediates that had been prepared using cycloaddition chemistry. Scaffold-hopping of these intermediates was achieved through attachment of an additional ring, ring cleavage, ring expansion and/or ring fusion. It was shown that the resulting scaffolds could be decorated to yield diverse lead-like screening compounds.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estrutura Molecular Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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