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Nucleophilic addition to olefins. 18. Kinetics of the addition of primary amines and .alpha.-effect nucleophiles to benzylidene Meldrum's acid

✍ Scribed by Bernasconi, Claude F.; Murray, Christopher J.


Book ID
121212980
Publisher
American Chemical Society
Year
1986
Tongue
English
Weight
839 KB
Volume
108
Category
Article
ISSN
0002-7863

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The influence of steric compression on electronic structure in polycyclic olefinic alcohols and amines is studied by PE. spectroscopy. The unsubstituted alcohol **2** and amine **7** show PE.‐spectroscopic properties that can be reconciled by postulating a predominance of intramolecularly H‐bonded

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## 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