N‐Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation
- 1 December 1996
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 35 (23-24), 2813-2817
- https://doi.org/10.1002/anie.199628131
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Osmiumkatalysierte asymmetrische Aminohydroxylierung: kleinere Substituenten am Stickstoffatom erleichtern die ReaktionAngewandte Chemie, 1996
- Smaller Substituents on Nitrogen Facilitate the Osmium‐Catalyzed Asymmetric AminohydroxylationAngewandte Chemie International Edition in English, 1996
- Katalytische asymmetrische Aminohydroxylierung (AA) von OlefinenAngewandte Chemie, 1996
- Catalytic Asymmetric Aminohydroxylation Provides a Short Taxol Side-chain Synthesis.Acta Chemica Scandinavica, 1996
- Ligandenbeschleunigte KatalyseAngewandte Chemie, 1995
- Novel access to (3R)- and (3S)-3-hydroxy-L-aspartic acids, (4S)-4-hydroxy- L-glutamic acid, and related amino acidsCanadian Journal of Chemistry, 1993
- Total Synthesis of the Biphenomycins; II.1Synthesis of Protected (2S,4R)-4-HydroxyornithinesSynthesis, 1991
- Efficient oxidation of phenyl groups to carboxylic acids with ruthenium tetraoxide. A simple synthesis of (R)-.gamma.-caprolactone, the pheromone of Trogoderma granariumThe Journal of Organic Chemistry, 1990
- Osmium-catalyzed vicinal oxyamination of olefins by N-chloro-N-argentocarbamatesJournal of the American Chemical Society, 1978
- Osmium-catalyzed vicinal oxyamination of olefins by Chloramine-TThe Journal of Organic Chemistry, 1976