Monobenzylethers of (R,R)-1,2-diphenylethane-1,2-diol as a possible alternative to cyclohexyl-based chiral auxiliaries in the stereoselective reduction of α-ketoesters
The monobenzylethers of (R,R)-1,2-diphenylethane-1,2-diol have been used as chiral auxiliaries in the stereoselective reduction of the corresponding phenylglyoxylates. The diastereoselectivity of the reduction with either L-selectride or DIBAL was found to be strictly dependent on the nature of the substitution on the aromatic ring of the auxiliary and a maximum d.r. of 87:13 was obtained with the p-CF3 substituted derivative. This investigation also shows that with open chain chiral auxiliaries diastereoselectivities of preparative interest can be achieved, suggesting that such auxiliaries can constitute a promising alternative to the commonest cyclohexyl-based ones.
Scafato, Patrizia,Leo, Laura,Superchi, Stefano,Rosini, Carlo
p. 153 - 159
(2007/10/03)
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