Diisopropyl tartrate (E)-γ-(dimethylphenylsilyl)allylboronate, a chiral allylic alcohol β-carbanion equivalent for the enantioselective synthesis of 2-butene-1,4-diols from aldehydes
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[1] W. Roush,et al. Asymmetric synthesis using diisopropyl tartrate modified (E)- and (Z)-crotylboronates: preparation of the chiral crotylboronates and reactions with achiral aldehydes , 1990 .
[2] W. Roush,et al. Asymmetric synthesis using tartrate ester modified allylboronates. 2. Single and double asymmetric reactions with alkoxy-substituted aldehydes , 1990 .
[3] R. Halcomb,et al. On the direct epoxidation of glycals: application of a reiterative strategy for the synthesis of .beta.-linked oligosaccharides , 1989 .
[4] J. Edwards,et al. Dioxiranes: a new class of powerful oxidants , 1989 .
[5] K. Burgess,et al. Stereoselective syntheses of γ-hydroxy-α,β-unsaturated esters: An asymmetric version of the “spac” reaction , 1989 .
[6] L. Raimondi,et al. Stereoselective synthesis of (e)-2-alkene-1,4-diols via metallated allylic sulphoxides , 1986 .
[7] D. Watt,et al. Synthesis of biological markers in fossil fuels. 2. Synthesis and carbon-13 NMR studies of substituted indans and tetralins , 1984 .
[8] I. Fleming,et al. The stereochemistry of some SE2′ reactions of allyl- and allenylsilanes☆ , 1983 .
[9] E. Corey,et al. Useful new organometallic reagents for the synthesis of allylic alcohols by nucleophilic vinylation , 1975 .