Cp2TiCl2-Catalyzed Grignard exchange reactions with acetylenes. A convenient method for preparation of E-alkenyl Grignard reagents
- 1 January 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (1) , 85-88
- https://doi.org/10.1016/0040-4039(81)80047-0
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Cp2TiCl2-catalyzed grignard exchange reactions with 1,3-dienes or styrenes. Preparation of allylic and α-arylethyl grignard reagents by a convenient and quantitative methodTetrahedron Letters, 1980
- Nickel-catalyzed addition of Grignard reagents to silylacetylenes. Synthesis of tetrasubstituted alkenesJournal of the American Chemical Society, 1978
- Hydrometallation of alkenes and alkynes with magnesium hydrideJournal of the Chemical Society, Chemical Communications, 1978
- Useful new organometallic reagents for the synthesis of allylic alcohols by nucleophilic vinylationThe Journal of Organic Chemistry, 1975
- Activations des reactifs de Grignard par les complexes du titane. Application du systeme “Cp2TiCl2—i-PrMgBr” comme agent reducteurJournal of Organometallic Chemistry, 1974
- Studies in group VI organometallic chemistry XXV. Necleophilic trans-addtition of organotin hydrides to carbon — carbon triple bonds.Journal of Organometallic Chemistry, 1967
- Synthetic Applications of the Titanium-Catalyzed Exchange of Olefins with Grignard Reagents1aThe Journal of Organic Chemistry, 1962