Electroreductive intermolecular coupling of ketones with O-methyl oximes. A convenient route to synthesis of 2-amino alcohols
- 1 January 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (4) , 525-528
- https://doi.org/10.1016/s0040-4039(00)79486-x
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Electroreductive intramolecular coupling of γ- and δ-cyanoketonesTetrahedron Letters, 1990
- Electroorganic chemistry. 118. Electroreductive intermolecular coupling of ketones with olefinsThe Journal of Organic Chemistry, 1989
- Reduction of Some Functional Groups with Zirconium Tetrachloride/Sodium BorohydrideSynthesis, 1988
- The first practical niobium(III) reagent in organic synthesis. A convenient route to 2-amino alcohols via the coupling of imines with aldehydes or ketones promoted by NbCl3(DME)Journal of the American Chemical Society, 1987
- Electroorganic chemistry. 98. Novel intramolecular stereoselective addition of electrogenerated radical species to the aromatic ringJournal of the American Chemical Society, 1986
- Electroorganic chemistry. 31. Reductive cyclization of nonconjugated olefinic ketones to cyclic tertiary alcoholsJournal of the American Chemical Society, 1978
- REDUCTIVE CYCLIZATION OF NONCONJUGATED ACETYLENIC KETONES TO 2- METHYLENECYCLOPENANOLSChemistry Letters, 1976