Kinetics and mechanism of the addition of allyl magnesium bromide to the double bond of cinnamyl alcohol. Catalysis by magnesium bromide.
β Scribed by Hugh Felkin; Christian Kaeseberg
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 207 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
The steric outcome of the reactions of simple cyclohexanones (e.g., 1) vith hydrides and Grignard reagents is governed by the relative magnitudes of the strains in the transition states At and E', leading to the axial ,2& and equatorial ZE alcohols respectively.le2 t BB" 'a 1 . 24
## 4, ' ) ' ) For solvent isotope effects in acid/base equilibria, see [lo]. For structural reasons, through-space interactions are negligible in such compounds. A steric effect was not detected by X-ray analysis. The interaction diagram was constructed according to the usual theoretical consider
## Abstract In view of the significance of steric compression in the baseβcatalyzed intramolecular cyclization of polycyclic olefinic alcohols, the standard enthalpies of formation of __anti__^9,10^β10 __endo__βhydroxytricyclo [4.2.1.1^2,5^]decaβ3,7βdienβ9βone **(1)** and 9βoxatetracyclo [5.4.0.0^3