Stereoselectivity in the amination of chiral cyclohex-3-en-1-one ketals
- 1 March 1997
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 53 (13), 4779-4786
- https://doi.org/10.1016/s0040-4020(97)00161-0
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Improved amination by ethyl n-(4-nitrophenyl)sulphonyloxy carbamate in the presence of inorganic oxides or carbonatesTetrahedron, 1994
- Cs2CO3 or CaO as promoters of ethyl N-{[(4-methylphenyl)sulphonyl]oxy}carbamate in amination reactionsTetrahedron, 1994
- A facile aziridination of allylic and homoallylic cyclic acetalsTetrahedron Letters, 1993
- Mechanistic studies of diastereoselective cyclopropanation via homochiral ketals. 1. Dioxolane structural effectsThe Journal of Organic Chemistry, 1990
- Mechanistic studies of diastereoselective cyclopropanation via homochiral ketals. 2. Studies with conformationally restricted 2-cyclohexen-1-one ketalsThe Journal of Organic Chemistry, 1990
- Functionalization of olefins by alkoximidoylnitrenesThe Journal of Organic Chemistry, 1989
- Homochiral ketals in organic synthesis. Diastereoselective cyclopropanation of α,β-unsaturated ketals derived from 1,4-D1-O-benzyl-l-threitolTetrahedron, 1987
- Selective imidoylnitrenesTetrahedron Letters, 1980
- Carbethoxynitrene by α-Elimination. Reactions with Hydrocarbons1,2Journal of the American Chemical Society, 1965
- The Decomposition of Ethyl Azidoformate in Cyclohexene and in Cyclohexane1Journal of the American Chemical Society, 1965