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Published TCIMAIL newest issue No.197 | Notice of Discontinuing the Use of Password-Protected Compressed Files | Various analytical charts can be searched on each product detail page and Product Document Search (The kinds of analytical charts differ by product)
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Rhodium(I)/(-)-DIOP Catalyzed Regio- and Enantioselective Addition of Carboxylic Acids to Allenes
Breit et al. have reported the first intermolecular regio- and enantioselective addition of carboxylic acids to terminal allenes to form branched allylic esters, employing a Rh(I)/(-)-DIOP catalyst system. Even 1,1-disubstituted allenes could be employed, leading to the formation of a quaternary chiral center. They have proposed the reaction proceeds through the Rh-π-allyl complex from the results of labeling experiments using deuterated benzoic acid.