C2-symmetric aziridines as efficient chiral auxiliaries
- 27 November 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (22), 2533-2536
- https://doi.org/10.1016/s0040-4039(00)74374-7
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- A versatile asymmetric synthesis of α-amino α-alkyl-phosphonic acids of high enantiomeric purityTetrahedron Letters, 1990
- Synthesis of (2R, 6R)-(−)-2,6-lupetidine: 2,6-disubstituted piperidines as potentially useful “C2-symmetric” chiral reagents.Tetrahedron Letters, 1990
- Enantioselective route to .gamma.-butyrolactones: chiral auxiliary mediated amide alkylation and iodolactonizationThe Journal of Organic Chemistry, 1990
- New enantioselective routes to biologically interesting compoundsPure and Applied Chemistry, 1990
- Enantioselective iodolactonization through diastereotopic group differentiationTetrahedron Letters, 1990
- C2 symmetry and asymmetric inductionChemical Reviews, 1989
- Symmetry and chiral recognition; separation of enantiomers on triacetyl-cellulose columnsTetrahedron, 1988
- Asymmetric [2,3]wittig rearrangement of 2′-alkenyloxyacetamide bearingTetrahedron Letters, 1986
- Asymmetric induction. 2. Enantioselective alkylation of cyclohexanone via a chiral enamineThe Journal of Organic Chemistry, 1977
- Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphineJournal of the American Chemical Society, 1972