Journal
ORGANIC LETTERS
Volume 8, Issue 20, Pages 4569-4572Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol061777l
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An enantio-, regio-, and diastereoselective rhodium(I)-catalyzed desymmetrization of a meso-cyclic allylic dicarbonate with organoboronic acid nucleophiles is described. The rhodium(I) catalyst formed in situ from [Rh(cod)OH](2) and Xyl-P-PHOS allowed the S(N)2' allylic substitution product to be obtained with a range of arylboronic acids in enantiomeric excesses of up to 92% with regioselectivities of up to > 20:1.
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