Issue 78, 2021

Copper-catalyzed enantioselective alkene carboetherification for the synthesis of saturated six-membered cyclic ethers

Abstract

The enantioselective copper-catalyzed oxidative coupling of alkenols with styrenes for the construction of dihydropyrans, isochromans, pyrans and morpholines is reported. A concise formal synthesis of a σ1 receptor ligand using this alkene carboetherification methodology was demonstrated. Ligand, solvent and base all impact reaction efficiency. DFT transition state calculations are presented.

Graphical abstract: Copper-catalyzed enantioselective alkene carboetherification for the synthesis of saturated six-membered cyclic ethers

Supplementary files

Article information

Article type
Communication
Submitted
01 Jul 2021
Accepted
06 Sep 2021
First published
06 Sep 2021

Chem. Commun., 2021,57, 10099-10102

Copper-catalyzed enantioselective alkene carboetherification for the synthesis of saturated six-membered cyclic ethers

I. A. Berhane, A. S. Burde, J. J. Kennedy-Ellis, E. Zurek and S. R. Chemler, Chem. Commun., 2021, 57, 10099 DOI: 10.1039/D1CC03515K

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