Abstract
The complexation of α-enones [(E)-MeC(H)C(H)COR] with SnCl4 and TiCl4 has been studied with NMR spectroscopy as well as semiempirical and ab initio SCF-MO methods, which indicate a preference for linear coordination of Lewis acids with α-enones due to the steric effect of R group (R = But, Ph, 2,4,6-Me3C6H2, 4-MeOC6H4) in the s-cis conformation.
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