期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 71, 期 26, 页码 9751-9764出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo062023n
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A comparative study of the carbonyl-ene reaction between a range of 1,1'-disubstituted or trisubstituted alkenes and ethyl trifluoropyruvate catalyzed by Lewis acid-platinum group metal complexes of the type [M{(R)-BINAP}](2+) (M = Pt, Pd, Ni; BINAP is 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl) revealed subtle but significant differences in their reactivity. For instance, the palladium-based Lewis acid [Pd{(R)-BINAP}](2+) catalyzes the ene reaction between methylene cycloalkane to afford the expected alpha-hydroxy ester in good yield and excellent diastereo- and enantioselectivity. In contrast, under the same conditions, the corresponding [M{(R)-BINAP}](2+) (M = Pt, Ni) catalyzes isomerization of methylene cycloalkane and the ene reaction of the resulting mixture of methylene cycloalkane and 1-methylcycloalkene at similar rates to afford a range of alpha-hydroxy esters in high regioselectivity, good diastereoselectivity, and good to excellent enantioselectivity. In addition, [Pt{(R)-BINAP}](2+) also catalyzes postreaction isomerization of the ene product as well as consecutive ene reactions to afford a double carbonyl-ene product. The sense of asymmetric induction has been established by single-crystal X-ray crystallography, and a stereochemical model consistent with the formation of (S)-configured alpha-hydroxy ester has been proposed; the same model also accounts for the observed exo-diastereoselectivity as well as the level of diastereoselectivity.
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