Highly stereoselective synthesis of cyclic primary amines via hydride reductions.
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (7), 695-698
- https://doi.org/10.1016/s0040-4039(01)80002-2
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Stereoselective reductions of substituted cyclohexyl and cyclopentyl carbon-nitrogen .pi. systems with hydride reagentsThe Journal of Organic Chemistry, 1983
- A general, highly stereoselective synthesis of aminesTetrahedron Letters, 1981
- Stereochemistry of nucleophilic addition to cyclohexanone. The importance of two-electron stabilizing interactionsJournal of the American Chemical Society, 1981
- The twist angle approach to the stereoselectivity in reduction of ketonesCanadian Journal of Chemistry, 1981
- Stereochemistry and mechanism of ketone reductions by hydride reagentsTetrahedron, 1979
- Reduction of Cyclic and Bicyclicc Ketones by Complex Metal HydridesTopics in Stereochemistry, 1979
- Potassium tri-isopropoxyborohydride. A new mild complex hydride reducing agent with high stereoselectivity for reduction of ketonesJournal of the Chemical Society, Chemical Communications, 1973
- Lithium tri-sec-butylborohydride. New reagent for the reduction of cyclic and bicyclic ketones with super stereoselectivity. Remarkably simple and practical procedure for the conversion of ketones to alcohols in exceptionally high stereochemical purityJournal of the American Chemical Society, 1972
- 11-Amino-Steroids. III. 11-Acetamido Derivatives of Cortexolone1-3The Journal of Organic Chemistry, 1966
- 11-Amino Steroids. II. 11-Amino- and 11-Acetamido-3,20-dioxypregnanes1The Journal of Organic Chemistry, 1966