Highly stereoselective radical addition to a trisubstituted alkene by low temperature photolysis of thiohydroxamic esters
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (12) , 1679-1682
- https://doi.org/10.1016/s0040-4039(00)88852-8
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Radical addition to amide-substituted alkenes: stereoselective intermolecular radical additionsJournal of the American Chemical Society, 1989
- The invention of radical reactionsTetrahedron, 1987
- Asymmetric induction. 2. Enantioselective alkylation of cyclohexanone via a chiral enamineThe Journal of Organic Chemistry, 1977
- Electron-Deficient Trisubstituted Olefins. A New Class of Reactive ComonomersMacromolecules, 1975
- Decarbalkoxylations of geminal diesters, β-keto esters and α-cyano esters effected by sodium chloride in dimethyl sulpoxideTetrahedron Letters, 1973
- On the homo Diels-Alder reaction of substituted norbornadienes as a possible route to longicyclene. : An intramolecular ene reaction.Tetrahedron Letters, 1973