6-Oxo-1,1,4,4-tetramethyl-1,4-diazepinium Salts. A New Class of Catalysts for Efficient Epoxidation of Olefins with Oxone
- 9 April 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (9) , 2810-2811
- https://doi.org/10.1021/jo980342b
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Highly Enantioselective Epoxidation of trans-Stilbenes Catalyzed by Chiral KetonesJournal of the American Chemical Society, 1996
- A C2 Symmetric Chiral Ketone for Catalytic Asymmetric Epoxidation of Unfunctionalized OlefinsJournal of the American Chemical Society, 1996
- An Efficient Asymmetric Epoxidation Method for trans-Olefins Mediated by a Fructose-Derived KetoneJournal of the American Chemical Society, 1996
- Epoxidation of Olefins Using Methyl(trifluoromethyl)dioxirane Generated in SituThe Journal of Organic Chemistry, 1995
- Catalytic Epoxidation of Alkenes with OxoneThe Journal of Organic Chemistry, 1995
- Dioxiranes: synthesis and reactions of methyldioxiranesThe Journal of Organic Chemistry, 1985
- Stereo- and regioselectivities in the epoxidation of some allylic alcohols by the dioxirane intermediate generated in the reaction of potassium caroate with acetoneThe Journal of Organic Chemistry, 1982
- Kinetics and mechanism of the oxidation of pyridine by Caro's acid catalyzed by ketonesThe Journal of Organic Chemistry, 1981
- Epoxidation of alkenes by dioxirane intermediates generated in the reaction of potassium caroate with ketonesThe Journal of Organic Chemistry, 1980
- ON THE FORMATION AND REACTIVITY OF DIOXIRANE INTERMEDIATES IN THE REACTION OF PEROXOANIONS WITH ORGANIC SUBSTRATES*Photochemistry and Photobiology, 1979