Competitive rate studies for some reactions involving the allyl, butenyl, αγ-dimethylallyl, and propyl Grignard reagents. the mechanism of the reactions of allylic Grignard reagents with electrophilic substrates.
- 31 December 1970
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 11 (13), 1045-1048
- https://doi.org/10.1016/s0040-4039(01)97903-1
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
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- Torsional strain involving partial bonds. The steric course of the reaction between allyl magnesium bromide and 4-t-butyl-cyclohexanoneTetrahedron Letters, 1968
- The stereochemical course of epoxide ring opening by allylic grignard reagentsTetrahedron Letters, 1965
- NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY. THE STRUCTURE OF BUTENYLMAGNESIUM BROMIDE1Journal of the American Chemical Society, 1961
- Allylic Rearrangements. XVI. The Addition of the Butenyl Grignard Reagent to Some Simple Carbonyl Compounds1Journal of the American Chemical Society, 1945