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Diastereodivergent and Regioselective Synthesis of Tetrahydrofuro[2,3-b]furans with Four Consecutive Stereocenters.
Zhang, Jing; Sun, Wen-Na; Jiang, Zhiwei; Jia, Shi-Kun; Mei, Guang-Jian.
Afiliação
  • Zhang J; Advanced Research Institute and School of Pharmaceutical Science, Taizhou University, Jiaojiang, Zhejiang 318000, P. R. China.
  • Sun WN; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou 450001, Henan,P. R. China.
  • Jiang Z; Advanced Research Institute and School of Pharmaceutical Science, Taizhou University, Jiaojiang, Zhejiang 318000, P. R. China.
  • Jia SK; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou 450001, Henan,P. R. China.
  • Mei GJ; Pingyuan Laboratory (Zhengzhou University), Zhengzhou 450001, P. R. China.
J Org Chem ; 89(6): 4134-4144, 2024 Mar 15.
Article em En | MEDLINE | ID: mdl-38394632
ABSTRACT
Base-catalyzed diastereodivergent and regioselective domino processes of triketone enones with arylacetaldehydes for the synthesis of tetrahydrofuro[2,3-b]furans with four consecutive stereocenters are reported. Good yields and diastereoselectivities are obtained when DBU is employed as a catalyst; in contrast, Et3N delivers a different diastereomer in excellent diastereoselectivity. This work offers many advantages, including switchable diastereoselectivity, cheap base catalysts, and a simple operation.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article