Synthesis of new, highly hindered C2-symmetric trans-(2S,5S)-disubstituted pyrrolidines
- 1 February 2002
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 13 (1), 87-93
- https://doi.org/10.1016/s0957-4166(02)00032-0
Abstract
No abstract availableThis publication has 57 references indexed in Scilit:
- The effect of polar substituents on the conformation and stereochemistry of enolate radicalsTetrahedron Letters, 1993
- Asymmetric vicinal acylation of olefins: A new approach to enantiomerically pure γ-lactones.Tetrahedron Letters, 1992
- Asymmetric induction in Manganese(III)-based oxidative free-radical cyclizations of chiral esters and amidesTetrahedron Letters, 1992
- The enantioselective fluoroacetamide acetal claisen rearrangements of N-fluoroacetyl-trans-(2R,5R)-2,5-dimethylpyrrolidineTetrahedron Letters, 1991
- Asymmetric amination of carboxylic acids via a diels-alder strategy.Tetrahedron Letters, 1991
- Study of chiral auxiliaries for the intramolecular [2+2] cycloaddition of a keteniminium salt to an olefinic double bond. A new asymmetric synthesis of cyclobutanones.Tetrahedron Letters, 1990
- C2 symmetry and asymmetric inductionChemical Reviews, 1989
- Radical addition to amide-substituted alkenes: stereoselective intermolecular radical additionsJournal of the American Chemical Society, 1989
- Highly diastereoselective alkylation reactions of vinylogous urethanes derived from simple tetronic acidsTetrahedron Letters, 1988
- Asymmetric induction. 2. Enantioselective alkylation of cyclohexanone via a chiral enamineThe Journal of Organic Chemistry, 1977