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    Correction: Substrate specificity of FUT8 and chemoenzymatic synthesis of core-fucosylated asymmetric N-glycans
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    Abstract:
    Correction for 'Substrate specificity of FUT8 and chemoenzymatic synthesis of core-fucosylated asymmetric N-glycans' by Angie D. Calderon et al., Org. Biomol. Chem., 2016, DOI: 10.1039/c6ob00586a.
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    The water-soluble steroid (I) acts as a catalyst for the hydrolysis of active esters, with a definite specificity for esters of 3-arylpropionic acids, the ester of 3-(3-phenanthryl)propionic acid being the most rapidly hydrolysed substrate found to date; it is concluded that imidazole-catalysed hydrolysis of the esters is facilitated by hydrophobic interactions between substrate and catalyst.
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    Abstract It is proposed that asymmetric syntheses be divided into enantioselective and diastereoselective syntheses. The enantioselective hydrogenations discussed in the present progress report were catalyzed by Raney nickel that had previously been treated with solutions of optically active compounds. Relationships exist between the enantioselectivity of the catalyst and the structure of the chiral compound used to modify it.
    Raney nickel
    Asymmetric hydrogenation
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    This review focuses on the enantioselective synthesis of halogenated molecules having a chiral halocarbon center. In particular, this review discusses enantioselective transformations with haloalkenes and enantioselective α-substitutions of α-halo carbonyl compounds. Enantioselective halogen-transfer reactions are excluded from this review.
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