Chiral 1,4-dihydropyridines. Synthesis and absolute configuration.
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (51) , 5123-5126
- https://doi.org/10.1016/s0040-4039(01)92436-0
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- High enantioselectivity in reductions with a chiral bis(NADH) model compoundJournal of the American Chemical Society, 1981
- Regioselective nucleophilic addition of organolithium compounds to 3-(4,4-dimethyloxazolin-2-yl)pyridineJournal of the Chemical Society, Perkin Transactions 1, 1980
- Reduction by a model of NAD(P)H. 25. A chiral model which induces high asymmetryJournal of the American Chemical Society, 1979
- Highly stereoselective addition of organolithium reagents to chiral oxazolines. Asymmetric synthesis of 3-substituted alkanoic acids and 3-substituted lactonesThe Journal of Organic Chemistry, 1979
- Asymmetric reductions with a chiral 1,4-dihydropyridine crown etherJournal of the American Chemical Society, 1979
- Oxazolines as Activating Groups in Aromatic Substitution. Selective Metalation or Addition to the 4-Position of Pyridine. A New Synthesis of 1,4-DihydropyridinesHETEROCYCLES, 1978