X=Y-ZH Systems as potential 1,3-dipoles. Part 39. Metallo-azomethine ylides from aliphatic aldimines. Facile regio- and stereo-specific cycloaddition reactions
- 1 November 1992
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 48 (47) , 10431-10442
- https://doi.org/10.1016/s0040-4020(01)88346-0
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Stereoselective Michael addition of the imines of .alpha.-amino esters in the presence of lithium bromide/1,8-diazabicyclo[5.4.0]undec-7-eneThe Journal of Organic Chemistry, 1990
- X=Y-ZH systems as potential 1,3-dipoles. Part 21 activation of the ZH proton in imines.Tetrahedron, 1989
- X=Y-ZH compounds as potential 1,3-dipoles. Part 24. Preparation and thermal fragmentation of imidazolidines. Influence of metal salts on pyrrolidine versus imidazolidine formationTetrahedron, 1989
- Ti(IV) mediated transesterification and regio- and stereo-specific cycloaddition of imines of α-amino esters. Reversal of normal regiochemistryTetrahedron Letters, 1989
- Lithium bromide-triethylamine induced cycloaddition of N-alkylidene 2-amino esters and amides to electron-deficient olefins with high regio- and stereoselectivityThe Journal of Organic Chemistry, 1988
- X-Y-ZH Systems as potential 1,3-dipolesTetrahedron, 1988
- X=Y-ZH systems as potential 1.3-dipolesTetrahedron, 1987
- Brönsted and Lewis acid catalysis of XY–ZH cycloadditionsJournal of the Chemical Society, Chemical Communications, 1982
- 5-Endo-trig cyclisation and 1,3-anionic cycloaddition in arylimine derivatives of α-amino acid estersJournal of the Chemical Society, Chemical Communications, 1980
- 1,3-Dipolar cycloaddition reactions of imines of α-amino-acid esters: X-ray crystal and molecular structure of methyl 4-(2-furyl)-2,7-diphenyl-6,8-dioxo-3,7-diazabicyclo[3.3.0]octane-2-carboxylateJournal of the Chemical Society, Chemical Communications, 1978