Abstract
Rh2(R-DOSP)4-catalyzed decomposition of methyl aryldiazoacetate in the presence of allyl silyl ethers results in a regioselective C−H insertion. The resulting β-siloxy esters are formed with high enantioselectivity (74−92% ee) and diastereoselectivity (96−98% de) when trans-disubstituted allyl silyl ethers are used as substrates.
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