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Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron.
Yasui, Masamichi; Hanaya, Kengo; Sugai, Takeshi; Higashibayashi, Shuhei.
Afiliação
  • Yasui M; Faculty of Pharmacy, Keio University 1-5-30 Shibakoen, Minato-ku Tokyo 105-8512 Japan higashibayashi-sh@pha.keio.ac.jp.
  • Hanaya K; Faculty of Pharmacy, Keio University 1-5-30 Shibakoen, Minato-ku Tokyo 105-8512 Japan higashibayashi-sh@pha.keio.ac.jp.
  • Sugai T; Faculty of Pharmacy, Keio University 1-5-30 Shibakoen, Minato-ku Tokyo 105-8512 Japan higashibayashi-sh@pha.keio.ac.jp.
  • Higashibayashi S; Faculty of Pharmacy, Keio University 1-5-30 Shibakoen, Minato-ku Tokyo 105-8512 Japan higashibayashi-sh@pha.keio.ac.jp.
RSC Adv ; 11(40): 24652-24655, 2021 Jul 13.
Article em En | MEDLINE | ID: mdl-35481014
The metal-free thermal organocatalytic pinacol coupling of arylaldehydes has been developed. The intermolecular coupling of arylaldehydes catalyzed by t-butyl isonicotinate with bis(pinacolato)diboron as the co-reducing agent afforded 1,2-diphenylethane-1,2-diols. This reaction was also applicable to the intramolecular coupling of 1,1'-biphenyl-2,2'-dicarbaldehydes to afford 9,10-dihydrophenanthrene-9,10-diols. Various functional groups were tolerated under this coupling condition.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article