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Anion-π catalysis on carbon allotropes.
Gutiérrez López, M Ángeles; Tan, Mei-Ling; Renno, Giacomo; Jozeliunaite, Augustina; Nué-Martinez, J Jonathan; Lopez-Andarias, Javier; Sakai, Naomi; Matile, Stefan.
Afiliação
  • Gutiérrez López MÁ; Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
  • Tan ML; Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
  • Renno G; Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
  • Jozeliunaite A; Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
  • Nué-Martinez JJ; Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
  • Lopez-Andarias J; Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
  • Sakai N; Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
  • Matile S; Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
Beilstein J Org Chem ; 19: 1881-1894, 2023.
Article em En | MEDLINE | ID: mdl-38116243
ABSTRACT
Anioncatalysis, introduced in 2013, stands for the stabilization of anionic transition states on π-acidic aromatic surfaces. Anioncatalysis on carbon allotropes is particularly attractive because high polarizability promises access to really strong anion-π interactions. With these expectations, anioncatalysis on fullerenes has been introduced in 2017, followed by carbon nanotubes in 2019. Consistent with expectations from theory, anioncatalysis on carbon allotropes generally increases with polarizability. Realized examples reach from enolate addition chemistry to asymmetric Diels-Alder reactions and autocatalytic ether cyclizations. Currently, anioncatalysis on carbon allotropes gains momentum because the combination with electric-field-assisted catalysis promises transformative impact on organic synthesis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Beilstein J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Beilstein J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Suíça