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Lipase-Catalyzed Kinetic Resolution of C1-Symmetric Heterocyclic Biaryls.
Kasama, Kengo; Hinami, Yuya; Mizuno, Karin; Horino, Satoshi; Nishio, Tomoya; Yuki, Chiharu; Kanomata, Kyohei; Moustafa, Gamal A I; Gröger, Harald; Akai, Shuji.
Afiliação
  • Kasama K; Graduate School of Pharmaceutical Sciences, Osaka University.
  • Hinami Y; Graduate School of Pharmaceutical Sciences, Osaka University.
  • Mizuno K; Graduate School of Pharmaceutical Sciences, Osaka University.
  • Horino S; Graduate School of Pharmaceutical Sciences, Osaka University.
  • Nishio T; Graduate School of Pharmaceutical Sciences, Osaka University.
  • Yuki C; Graduate School of Pharmaceutical Sciences, Osaka University.
  • Kanomata K; Graduate School of Pharmaceutical Sciences, Osaka University.
  • Moustafa GAI; Graduate School of Pharmaceutical Sciences, Osaka University.
  • Gröger H; Department of Medicinal Chemistry, Faculty of Pharmacy, Minia University.
  • Akai S; Chair of Industrial Organic Chemistry and Biotechnology, Faculty of Chemistry, Bielefeld University.
Chem Pharm Bull (Tokyo) ; 70(5): 391-399, 2022.
Article em En | MEDLINE | ID: mdl-35491196
ABSTRACT
The highly enantioselective lipase-catalyzed kinetic resolution (KR) of racemic C1-symmetric biaryl compounds including heterocyclic moieties, such as carbazole and dibenzofuran, has been achieved for the first time. This enzymatic esterification was accelerated by the addition of disodium carbonate while maintaining its high enantioselectivities, and was particularly effective for biaryls having N-substituted carbazole moieties. Furthermore, mesoporous silica-supported oxovanadium-catalyzed cross-dehydrogenative coupling of 3-hydroxycarbazole and 2-naphthol was followed by the lipase-catalyzed KR in one-pot to synthesize the optically active heterocyclic biaryl compounds with high optical purity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carbazóis / Lipase Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carbazóis / Lipase Idioma: En Ano de publicação: 2022 Tipo de documento: Article