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• W2313961434 abstract "Highly efficient pseudo-enantiomeric olefin ligands were designed from d-glucose and d-galactose. These ligands yield consistently excellent levels of enantioselectivity in Rh(I)-catalyzed 1,4-additions of aryl- and alkenylboronic acids to achiral enones and high diastereoselectivity with chiral substrates. Contrary to established olefin ligands, they are obtained enantiomerically pure via short syntheses without racemic resolution steps, making them a valuable addition to the arsenal of chiral ligands with olefinic donor sites." @default.
• W2313961434 created "2016-06-24" @default.
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• W2313961434 date "2012-07-10" @default.
• W2313961434 modified "2023-10-09" @default.
• W2313961434 title "Efficient Pseudo-enantiomeric Carbohydrate Olefin Ligands" @default.
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• W2313961434 doi "https://doi.org/10.1021/ol3015896" @default.
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• W2313961434 hasPublicationYear "2012" @default.
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