Enantio- and Diastereoselective Copper-Catalyzed Borylative Coupling of Styrenes and Azadienes

Here we disclose a CuB-catalyzed reaction between aurone-derived α,β-unsaturated imines and styrenes to produce 2-substituted benzofuran derivatives bearing both the γ-boryl functionality and α,β-unsymmetric stereogenic centers. The reaction represents the first transition-metal-catalyzed unsymmetri...

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Veröffentlicht in:Organic letters 2024-06, Vol.26 (25), p.5335-5340
Hauptverfasser: Xie, Fang, Dong, Shijie, Liu, Jiayi, Yu, Miao, Ren, Deyue, Zhao, Jie, Liu, Xiaodan
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Sprache:eng
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Zusammenfassung:Here we disclose a CuB-catalyzed reaction between aurone-derived α,β-unsaturated imines and styrenes to produce 2-substituted benzofuran derivatives bearing both the γ-boryl functionality and α,β-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.
ISSN:1523-7060
1523-7052
1523-7052
DOI:10.1021/acs.orglett.4c01722