| Literature DB >> 26273792 |
Bin Wang1, Yong-Min Lee1, Mi Sook Seo1, Wonwoo Nam2.
Abstract
High-spin iron(III)-iodosylarene complexes are highly reactive in the epoxidation of olefins, in which epoxides are formed as the major products with high stereospecificity and enantioselectivity. The reactivity of the iron(III)-iodosylarene intermediates is much greater than that of the corresponding iron(IV)-oxo complex in these reactions. The iron(III)-iodosylarene species-not high-valent iron(IV)-oxo and iron(V)-oxo species-are also shown to be the active oxidants in catalytic olefin epoxidation reactions. The present results are discussed in light of the long-standing controversy on the one oxidant versus multiple oxidants hypothesis in oxidation reactions.Entities:
Keywords: bioinorganic chemistry; enzyme models; epoxidation; iron complexes; reaction mechanisms
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Year: 2015 PMID: 26273792 DOI: 10.1002/anie.201505796
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336