Issue 7, 2020

Iron-catalyzed stereospecific arylation of enol tosylates using Grignard reagents

Abstract

The stereospecific Fe-catalyzed arylation of enol tosylates was reported. Various tri- or tetrasubstituted Z or E-enol tosylates of β-keto esters were arylated using common and Knochel-type Grignard reagents with complete stereofidelity. The precursors for Z/E-zimelidine, tamoxifen and other bioactive compounds were facilely prepared without precious and toxic transition metals.

Graphical abstract: Iron-catalyzed stereospecific arylation of enol tosylates using Grignard reagents

Supplementary files

Article information

Article type
Communication
Submitted
09 Dec 2019
Accepted
16 Dec 2019
First published
17 Dec 2019

Chem. Commun., 2020,56, 1101-1104

Iron-catalyzed stereospecific arylation of enol tosylates using Grignard reagents

Y. Wei, X. Ma, L. Wang and X. Duan, Chem. Commun., 2020, 56, 1101 DOI: 10.1039/C9CC09522E

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