Copper-Catalyzed Defluorinative Borylation and Silylation of <i>gem</i>-Difluoroallyl Groups.

ABSTRACT: Stereodefined (Z)-fluoroalkenes are bioisosteres of amides and synthetic precursors to value-added fluorinated compounds, but their stereoselective synthesis remains challenging. Herein, we report a copper-catalyzed formal S_N2' defluorinative borylation of 3-substituted 3,3-difluoropropenes to form 3-fluoroallylboronic esters in high yields with excellent Z/E ratios. The primary 3-fluoroallylboronic esters undergo several synthetic sequences involving S_E2' substitutions, S_N2' substitutions, and sigmatropic rearrangements to provide tertiary allylic fluorides.

SUBMITTER: Butcher TW 

PROVIDER: S-EPMC11620733 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature