Tricarbonyl(benzaldehyde)chromium(0) complexes in organic synthesis: A highly stereoselective 1,3-dipolar cycloaddition of chromium(0)-complexed nitrones
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (47) , 6893-6896
- https://doi.org/10.1016/s0040-4039(00)97200-9
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Asymmetric synthesis of alpha substituted benzyl alcohols via the stereoselective addition of nucleophiles to homochiral tricarbonyl(η6-o-trialkylsilylbenzaldehyde)chromium(0) complexesJournal of the Chemical Society, Perkin Transactions 1, 1990
- A highly erythro selective aldol reaction between chromium-complexed benzaldehyde derivatives and cyclic silyl enol ethersTetrahedron Letters, 1989
- Nitrone cycloadditions. An efficient method for the homologation of aldehydes to .alpha.,.beta.-unsaturated aldehydesThe Journal of Organic Chemistry, 1984
- Reactions at high pressures. [3+2] Dipolar cycloaddition of nitrones with vinyl ethersThe Journal of Organic Chemistry, 1982
- Alkaloids from nitronesAccounts of Chemical Research, 1979
- .eta.5-Cyclohexadienyltricarbonylchromium(0) complexes from addition of carbon nucleophiles to .eta.6-benzenetricarbonylchromium(0). Formation, chemical and spectroscopic features, and x-ray diffraction analysisJournal of the American Chemical Society, 1979
- 1.3‐Dipolare Cycloadditionen, XLI. Anlagerung der Nitrone an Styrol; Orientierung und räumlicher AblaufEuropean Journal of Inorganic Chemistry, 1968