Duality of mechanism in the addition of allylic grignard reagents to carbon-carbon double bonds. The stereoselective cyclisation of 2,7-octadienylmagnesium bromide to cis-(2-vinylcyclopentyl)-methylmagnesium bromide
- 31 December 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (22) , 2285-2288
- https://doi.org/10.1016/s0040-4039(01)84829-2
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Addition von organomagnesium-verbindungen an nicht aktivierte CC-doppelbindungen. IIJournal of Organometallic Chemistry, 1972
- The stereochemistry of additions of grignard reagents to alkynolsTetrahedron Letters, 1971
- Nuclear magnetic resonance spectroscopy. Carbon-13 chemical shifts of methycyclopentanes, cyclopentanols, and cyclopentyl acetatesJournal of the American Chemical Society, 1971
- Promotion by primary and tertiary amine functions of additions of grignard reagents to alkenes and alkynesTetrahedron Letters, 1971
- Die addition von allylmagnesium-halogeniden an 1-alkeneJournal of Organometallic Chemistry, 1970
- Kinetics and mechanism of the addition of allyl magnesium bromide to the double bond of cinnamyl alcohol. Catalysis by magnesium bromide.Tetrahedron Letters, 1970
- Promotion by hydroxyl functions of additions of Grignard reagents to alkynesJournal of Organometallic Chemistry, 1969
- Addition of organolithium reagents to the double bond of allylic alcoholsTetrahedron Letters, 1969
- Addition of grignard reagents to the double bond of allylic alcoholsTetrahedron Letters, 1966
- Facile Addition of a Grignard Reagent to an Unconjugated Ethylenic LinkageJournal of the American Chemical Society, 1965