Heterodienophiles 9. On the preference for -orientation in aldimine cycloadditions
- 31 December 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (23) , 1971-1974
- https://doi.org/10.1016/s0040-4039(01)94724-0
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- A Diels-Alder approach to the pyridine C ring of streptonigrinThe Journal of Organic Chemistry, 1978
- The regioselectivity of the catalyzed and uncatalyzed Diels-Alder reactionJournal of the American Chemical Society, 1977
- Synthetic studies in the piperidine alkaloid field. Part 1. The 2-azabicyclo[2.2.2]octan-5-one approach to prosopineJournal of the Chemical Society, Perkin Transactions 1, 1977
- Catalysed Diels–Alder reactions. The realization of orientation control with a bifunctional aliphatic dienophileCanadian Journal of Chemistry, 1976
- Synthese du squelette des cannivoninesTetrahedron Letters, 1976
- Heterodienophiles. VI. Structure of protonated aldiminesThe Journal of Organic Chemistry, 1974
- Heterodienophiles—VTetrahedron, 1974
- Heterodienophiles. I. Stereoselectivity in the 1,4-addition of iminocarbamates to cyclohexa-1,3-dieneJournal of the American Chemical Society, 1973
- Lewis acid catalysis of Diels-Alder reactionsJournal of the American Chemical Society, 1973
- Einfluss von lewis-säuren auf das endo-exo-verhaltnis bei diels-alder-additionen des cyclopentadiensTetrahedron Letters, 1966