Tandem nucleophilic substitution - 1,3 dipolar cycloaddition reactions of oximes with epoxides and dipolarophiles
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (40) , 5489-5492
- https://doi.org/10.1016/s0040-4039(01)80601-8
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- A route to pyrrolizidines, indolizidines and quinolizidines via intramolecular oxime olefin cycloadditionsTetrahedron Letters, 1989
- Consecutive diels-alder- michael addition - 1,3-dipolar cycloaddition processesTetrahedron Letters, 1989
- Regio- and stereo-specific class 2 tandem Michael addition-cycloaddition reactions of oximesTetrahedron Letters, 1988
- Formation of functionalized cyclic ethers by intramolecular nitrile oxide cycloadditionsTetrahedron Letters, 1988
- Intramolecular oxime olefin cycloadditions. Stereospecific formation of functionalized pyrrolidines.Tetrahedron Letters, 1988
- Intramolecular cycloaddition reactions of oximes with vinyl sulfonesTetrahedron Letters, 1988
- Novel transformations leading to 3-benzylindolizidin-2-onesThe Journal of Organic Chemistry, 1987
- Tandem intramolecular Michael addition and 1,3-dipolar cycloaddition reactions of oximes; versatile new carbon–carbon bond forming methodologyJournal of the Chemical Society, Chemical Communications, 1987
- Cycloaddition reactions of oximes; powerful new carbon–carbon bond forming methodologyJournal of the Chemical Society, Chemical Communications, 1987
- 6-Hydroxybuphanidrine and 6-hydroxypowellineThe Journal of Organic Chemistry, 1971