1,3-Asymmetric induction: Highly enantioselective synthesis of α-amino acids via 2,5-trans disubstituted imidazolidin-4-ones
- 22 April 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (17) , 1971-1974
- https://doi.org/10.1016/0040-4039(91)85016-x
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Synthesis of L and D α-amino acids from chiral amidalsTetrahedron Letters, 1990
- Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediatesTetrahedron, 1990
- Sequential chirality transfer in intramolecular amidomercuration reactionsTetrahedron Letters, 1989
- A removable auxiliary for amidomercuration reactions: The stereocontrolled preparation of vicinal aminoalcoholsTetrahedron Letters, 1989
- Synthesis of Aminoalcohols via Perihydro-1,3-oxazin-2-ones and Absolute Configuration Assignment through MM2 CalculationsChemistry Letters, 1988
- Applications of intramolecular amidomercuration. 3. Stereoselectivity in intramolecular amidomercuration. Kinetic vs. thermodynamic controlThe Journal of Organic Chemistry, 1984
- 1,3-Asymmetric induction: highly stereoselective synthesis of 2,4-trans-disubstituted γ-butyrolactones and γ-butyrothiolactonesJournal of the American Chemical Society, 1984
- Applications of intramolecular amidomercuration. 2. Synthesis of trans-5-hydroxy-2-propylpiperidine, (.+-.)-pseudoconhydrineThe Journal of Organic Chemistry, 1984
- Stereocontrolled synthesis of cis-2,5-disubstituted tetrahydrofurans and cis- and trans-linalyl oxidesJournal of the American Chemical Society, 1981
- Synthesis of N-substituted aziridine-2-carboxylatesTetrahedron, 1977