Literature DB >> 31553003

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

Taoda Shi1, Shenghan Teng2, Alavala Gopi Krishna Reddy3, Xin Guo4, Yueteng Zhang5, Kohlson T Moore5, Thomas Buckley5, Damian J Mason5, Wei Wang5, Eli Chapman5, Wenhao Hu3.   

Abstract

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](AgSbF6)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.

Entities:  

Year:  2019        PMID: 31553003     DOI: 10.1039/c9ob01903k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Theoretical study on the mechanism, chemo- and enantioselectivity of the Ag- vs. Rh-catalyzed intramolecular carbene transfer reaction of diazoacetamides.

Authors:  Qingmin Song; Jiayi Wu; Nikolaos V Tzoukras; Yong Wu; Steven P Nolan
Journal:  RSC Adv       Date:  2022-06-22       Impact factor: 4.036

  1 in total

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