Regio- and stereoselective epoxidation of chiral 1,4-cyclohexadienes
- 6 October 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (41) , 6097-6100
- https://doi.org/10.1016/s0040-4039(00)60015-1
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Substituent effects on the photorearrangements of 4-alkoxy-4-carbomethoxy-3-methoxy-2,5-cyclohexadien-1-onesThe Journal of Organic Chemistry, 1991
- Relative oxygen donor potential of dioxirane and carbonyl oxide. A theoretical studyJournal of the American Chemical Society, 1991
- Enantioselective methods for chiral cyclohexane ring synthesisAccounts of Chemical Research, 1990
- Dimethyldioxirane epoxidation of α,β-unsaturated ketones, acids and esters.Tetrahedron Letters, 1990
- Dimethyldioxirane: Mechanism of benzaldehyde oxidationTetrahedron Letters, 1989
- Chemistry of dioxiranes. 13. Oxidation of primary amines by dimethyldioxiraneThe Journal of Organic Chemistry, 1989
- Dioxiranes: a new class of powerful oxidantsAccounts of Chemical Research, 1989
- An enantioselective method for reductive alkylation of aromatic carboxylic acid derivatives. Examination of the factors that provide stereoselectivityJournal of the American Chemical Society, 1988
- Chemistry of dioxiranes. 4. Oxygen atom insertion into carbon-hydrogen bonds by dimethyldioxiraneJournal of the American Chemical Society, 1986
- 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