Electrophilic Amination of Ketone Enolates Mediated by the DiTOX Asymmetric Building Block: Enantioselective Formal Synthesis of α-Aminoacids
- 29 November 2000
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 56 (49) , 9683-9695
- https://doi.org/10.1016/s0040-4020(00)00923-6
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Highly chemoselective osmium-mediated dihydroxylation of 2-vinyl and 2-allyl-1,3-dithiane 1-oxidesTetrahedron, 1998
- Asymmetric synthesis of α-amino acid derivatives via an electrophilic amination of chiral amide cuprates with Li t-butyl-N-tosyloxycarbamateTetrahedron Letters, 1997
- The Reaction of [N-(p-Toluenesulfonyl)Imino]-Phenyliodinane with Enol SilanesSynthetic Communications, 1996
- New trialkylsilyl enol ether chemistry: α-N-tosylamination of triisopropylsilyl enol ethersTetrahedron, 1995
- Oxidative addition of azide anion to triisopropylsilyl enol ethers: Synthesis of α-azido ketones and 2-amino(methoxycarbonyl)alk-2-en-1-onesTetrahedron, 1995
- Highly Enantioselective Catalytic Asymmetric Oxidation of Sulfides using Hydrogen PeroxideSynlett, 1995
- Electrophilic amination reagents: A new method for the preparation of 3-Aryl-N-BOC (or N-FMOC) oxaziridinesTetrahedron Letters, 1995
- Mesyl azide: a superior reagent for diazo transferThe Journal of Organic Chemistry, 1986
- Reaction of ketene silyl acetals with diazonium salts: a novel α-amino acid ester synthesisJournal of the Chemical Society, Chemical Communications, 1985
- Synthetic methods. VI. Addition of nitrosyl chloride to trimethylsilyl enol ethers. New general method for nitrosation of carbonyl compoundsThe Journal of Organic Chemistry, 1974