Lewis acid mediated additions to Fe(CO)3-2,4-dienal complexes are explored. Silyl enol ether and allylstannane nucleophiles both undergo aldehyde addition with good diastereoselectivity. However, with TiCl4 as the catalyst, the psi-exo diastereomer is the major product while with BF3.Et2O the psi-endo diastereomer is favored. Lewis acid/substrate interactions are studied by VT-NMR, and a hypothesis that accounts for the observed diastereoselectivity is presented.
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Harvey et al. (2000) studied this question.
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