Rationalising diastereoselection in the dynamic kinetic resolution of α-haloacyl imidazolidinones
- 1 April 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (15) , 2203-2206
- https://doi.org/10.1016/s0040-4039(98)00175-0
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Dynamic Kinetic Resolution Utilizing 2-Oxoimidazolidine-4-carboxylate as a Chiral Auxiliary: Stereoselective Alkylation of α-Bromo Amides with Malonic Ester EnolatesThe Journal of Organic Chemistry, 1997
- (R)- and (S)-3-hydroxy-4,4-dimethyl-1-phenyl-2-pyrrolidinone as chiral auxiliaries for the asymmetric synthesis of α-hydroxy acidsTetrahedron: Asymmetry, 1997
- A new dynamic resolution strategy for asymmetric synthesisTetrahedron Letters, 1996
- Dynamic resolutions in asymmetric synthesisChemical Society Reviews, 1996
- Stereospecific Amination by Dynamic Kinetic Resolution Utilizing 2-Oxoimidazolidine-4-carboxylate as a Novel Chiral AuxiliaryThe Journal of Organic Chemistry, 1995
- Dynamic kinetic resolutionTetrahedron: Asymmetry, 1995
- Diastereoselective synthesis of α-bromo amides leading to diastereomerically enriched α-amino-, α-hydroxy- and α-thiocarboxylic acid derivativesTetrahedron: Asymmetry, 1995
- Stereoselective Organic Synthesis via Dynamic Kinetic ResolutionBulletin of the Chemical Society of Japan, 1995
- Rates and salt effects in the reactions of phenacyl bromide with N-ethylaniline and triethylamine in chloroformJournal of the American Chemical Society, 1968
- Mechanism of the Reaction of α-Haloketones with Weakley Basic Nucleophilic ReagentsJournal of the American Chemical Society, 1952