Catalytic asymmetric synthesis of 2,5-dihydrofurans using synergistic bifunctional Ag catalysis

We report a bifunctional Ag catalyst promoted intramolecular capture of oxonium ylides with alkynes for the enantioselective synthesis of 2,5-dihydrofurans. This represents unprecedented synergistic catalysis of a bifunctional Ag catalyst. Mechanistic studies revealed that [( R )-3,5-DM-BINAP](AgSbF...

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Veröffentlicht in:Organic & biomolecular chemistry 2019-10, Vol.17 (38), p.8737-8744
Hauptverfasser: Shi, Taoda, Teng, Shenghan, Gopi Krishna Reddy, Alavala, Guo, Xin, Zhang, Yueteng, Moore, Kohlson T, Buckley, Thomas, Mason, Damian J, Wang, Wei, Chapman, Eli, Hu, Wenhao
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Sprache:eng
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Zusammenfassung:We report a bifunctional Ag catalyst promoted intramolecular capture of oxonium ylides with alkynes for the enantioselective synthesis of 2,5-dihydrofurans. This represents unprecedented synergistic catalysis of a bifunctional Ag catalyst. Mechanistic studies revealed that [( R )-3,5-DM-BINAP](AgSbF 6 ) 2 ( 9 ) is likely to be the active catalytic species and that the reaction involves second order kinetics with respect to 9 , suggesting that two molecules of 9 are involved in the intramolecular trapping of a Ag-associated oxonium ylide with a Ag-activated alkyne. Based on our mechanistic hypothesis, we further optimized the reaction, rendering a facile approach to 2,5-dihydrofurans in good to excellent yields in a highly chemo- and enantioselective fashion. We report a bifunctional Ag catalyst promoted intramolecular capture of oxonium ylides with alkynes for the enantioselective synthesis of 2,5-dihydrofurans.
ISSN:1477-0520
1477-0539
DOI:10.1039/c9ob01903k