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Remote OH-group directing effect in the stereochemistry of intramolecular alkoxide addition to conjugated double bond

✍ Scribed by I. Tömösközi; G. Galambos; G. Kovács; L. Gruber


Publisher
Elsevier Science
Year
1979
Tongue
French
Weight
220 KB
Volume
20
Category
Article
ISSN
0040-4039

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✦ Synopsis


Preferential formation of less stable (endo) product in intramolecular MichaeZ reaction is explained by the participation

of structuraZZy remote OH group in the transition state.