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Enantio- and Diastereoselective Copper-Catalyzed Borylative Coupling of Styrenes and Azadienes.
Xie, Fang; Dong, Shijie; Liu, Jiayi; Yu, Miao; Ren, Deyue; Zhao, Jie; Liu, Xiaodan.
Affiliation
  • Xie F; School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165, China.
  • Dong S; School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165, China.
  • Liu J; School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165, China.
  • Yu M; School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165, China.
  • Ren D; School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165, China.
  • Zhao J; School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165, China.
  • Liu X; School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165, China.
Org Lett ; 26(25): 5335-5340, 2024 Jun 28.
Article in En | MEDLINE | ID: mdl-38885466
ABSTRACT
Here we disclose a CuB-catalyzed reaction between aurone-derived α,ß-unsaturated imines and styrenes to produce 2-substituted benzofuran derivatives bearing both the γ-boryl functionality and α,ß-unsymmetric stereogenic centers. The reaction represents the first transition-metal-catalyzed unsymmetric 1,4-Michael additions of azadienes, which would enrich the arsenal of CuB catalysis in organic synthesis. In addition, the synthetically versatile boron-alkylated products can be elaborated by chemical transformations to useful optically active benzofuran heterocycles.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2024 Document type: Article Affiliation country: China