Iodine-catalyzed aziridination of alkenes using Chloramine-T as a nitrogen source
- 1 October 1998
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 54 (44) , 13485-13494
- https://doi.org/10.1016/s0040-4020(98)00827-8
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Bromine-Catalyzed Aziridination of Olefins. A Rare Example of Atom-Transfer Redox Catalysis by a Main Group ElementJournal of the American Chemical Society, 1998
- A Highly Efficient Aminohydroxylation ProcessAngewandte Chemie International Edition in English, 1997
- N‐Bromoacetamide—A New Nitrogen Source for the Catalytic Asymmetric Aminohydroxylation of OlefinsAngewandte Chemie International Edition in English, 1997
- Smaller Substituents on Nitrogen Facilitate the Osmium‐Catalyzed Asymmetric AminohydroxylationAngewandte Chemie International Edition in English, 1996
- 1,2-Diamination of 1,3-dienes by imido selenium compoundsThe Journal of Organic Chemistry, 1976
- Osmium-catalyzed vicinal oxyamination of olefins by Chloramine-TThe Journal of Organic Chemistry, 1976
- Improved Preparation ofS,S-Dimethyl-N-arylsulfonylsulfoximines1Synthesis, 1976
- Ethylenimine Ketones. XI.1 Steric Controls in the Formation of Isomeric Ethylenimine KetonesJournal of the American Chemical Society, 1957
- Ethylenimine Ketones. X. The Stereoisomerism of 1-Cyclohexyl-2-methyl-3-(p-phenylbenzoyl)-ethylenimine1Journal of the American Chemical Society, 1953
- Reactions of Unsaturated Compounds with Iodine—Amine Complexes. I. Reactions of Benzalacetophenone and BenzalacetoneJournal of the American Chemical Society, 1952