z-logo
open-access-imgOpen Access
Formal Enone α-Arylation via I(III)-Mediated Aryl Migration/Elimination
Author(s) -
Bruna S. Martins,
Daniel Kaiser,
Adriano Bauer,
Irmgard Tiefenbrunner,
Nuno Maulide
Publication year - 2021
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/acs.orglett.1c00251
Subject(s) - enone , chemistry , enol , aryl , silylation , formal synthesis , transformation (genetics) , combinatorial chemistry , stereochemistry , catalysis , organic chemistry , biochemistry , alkyl , gene
A formal enone α-arylation is described. This metal-free transformation relies on the I(III)-mediated skeletal reorganization of silyl enol ethers and features mild conditions, good yields, and high stereoselectivities for β-substituted enones.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom