Iron Catalyzed Highly Enantioselective Epoxidation of Cyclic Aliphatic Enones with Aqueous H2O2

Olaf Cussó, Marco Cianfanelli, Xavi Ribas, Robertus J M Klein Gebbink*, Miquel Costas*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

An iron complex with a C1-symmetric tetradentate N-based ligand catalyzes the asymmetric epoxidation of cyclic enones and cyclohexene ketones with aqueous hydrogen peroxide, providing the corresponding epoxides in good to excellent yields and enantioselectivities (up to 99% yield, and 95% ee), under mild conditions and in short reaction times. Evidence is provided that reactions involve an electrophilic oxidant, and this element is employed in performing site selective epoxidation of enones containing two alkene sites.

Original languageEnglish
Pages (from-to)2732–2738
Number of pages7
JournalJournal of the American Chemical Society
Volume138
Issue number8
DOIs
Publication statusPublished - 2 Mar 2016

Fingerprint

Dive into the research topics of 'Iron Catalyzed Highly Enantioselective Epoxidation of Cyclic Aliphatic Enones with Aqueous H2O2'. Together they form a unique fingerprint.

Cite this