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Chiral-Anion-Dependent Inversion of Diastereo- and Enantioselectivity in Carbonyl Crotylation via Ruthenium-Catalyzed Butadiene Hydrohydroxyalkylation

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NIAID Data Ecosystem2026-03-07 收录
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https://figshare.com/articles/dataset/Chiral_Anion_Dependent_Inversion_of_Diastereo_and_Enantioselectivity_in_Carbonyl_Crotylation_via_Ruthenium_Catalyzed_Butadiene_Hydrohydroxyalkylation/2457511
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The ruthenium catalyst generated in situ from H2Ru­(CO)­(PPh3)3, (S)-SEGPHOS, and a TADDOL-derived phosphoric acid promotes butadiene hydrohydroxyalkylation to form enantiomerically enriched products. Notably, the observed diastereo- and enantioselectivity is the opposite of that observed using BINOL-derived phosphate counterions in combination with (S)-SEGPHOS, the same enantiomer of the chiral ligand. Match/mismatch effects between the chiral ligand and the chiral TADDOL-phosphate counterion are described. For the first time, single-crystal X-ray diffraction data for a ruthenium complex modified by a chiral phosphate counterion are reported.
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2012-12-26
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