Umlagerung von Allyl??aryläthern und Allyl??cyclohexadienonen mittels Bortrichlorid

J Borgulya, R Madeja, P Fahrni…

Index: Borgulya,J. et al. Helvetica Chimica Acta, 1973 , vol. 56, # 1 p. 14 - 75

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Citation Number: 76

Abstract

Abstract Allyl aryl ethers which have no strongly electron attracting substituents undergo a charge-induced [3 s, 3 s] sigmatropic rearrangement in the prescence of 0.7 mole boron trichloride in chlorobenzene at low temperature, to give after hydrolysis the corresponding o- allyl phenols (Tables 1 and 2). The charge induction causes an increase in the reaction rate relative to the thermal Claisen rearrangement of∼ 10 10. With the exception of allyl 3- ...