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Aerobic oxidative synthesis of quinazolinones and benzothiazoles in the presence of laccase/DDQ as a bioinspired cooperative catalytic system under mild conditions.
Ghorashi, Nadia; Shokri, Zahra; Moradi, Reza; Abdelrasoul, Amira; Rostami, Amin.
Afiliação
  • Ghorashi N; Department of Chemistry, Faculty of Science, University of Kurdistan 66177-15175 Sanandaj Iran a_rostami372@yahoo.com +988716624004 +989183730910.
  • Shokri Z; Department of Chemistry, Faculty of Science, University of Kurdistan 66177-15175 Sanandaj Iran a_rostami372@yahoo.com +988716624004 +989183730910.
  • Moradi R; Department of Chemistry, Faculty of Science, University of Kurdistan 66177-15175 Sanandaj Iran a_rostami372@yahoo.com +988716624004 +989183730910.
  • Abdelrasoul A; Department of Chemical and Biological Engineering, University of Saskatchewan 57 Campus Drive Saskatoon Saskatchewan S7N 5A9 Canada.
  • Rostami A; Department of Chemistry, Faculty of Science, University of Kurdistan 66177-15175 Sanandaj Iran a_rostami372@yahoo.com +988716624004 +989183730910.
RSC Adv ; 10(24): 14254-14261, 2020 Apr 06.
Article em En | MEDLINE | ID: mdl-35498453
The current study applied laccase/DDQ as a bioinspired cooperative catalytic system for the synthesis of quinazolinones (80-95% yield) and benzothiazoles (65-98% yield) using air or O2 as ideal oxidants in aqueous media at ambient temperature. The aerobic oxidative cyclization reactions occur in two steps: (i) chemical cyclization; (ii) chemoenzymatic oxidation. These methods are more environment-friendly, efficient, simple and practical than other reported methods due to the use of O2 as an oxidant, laccase as an eco-friendly biocatalyst, aqueous media as the solvent and free from any toxic transition metal and halide catalysts. Therefore, these methods can be applied in pharmaceutical and other sensitive synthetic procedures.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2020 Tipo de documento: Article