Fig. 6: Enantioconvergent hydrogenation of trisubstituted unsaturated enones. | Nature Communications

Fig. 6: Enantioconvergent hydrogenation of trisubstituted unsaturated enones.

From: Iridium-catalyzed enantioconvergent hydrogenation of trisubstituted olefins

Fig. 6

Reaction conditions: 0.1 mmol substrate, 1.0 mol% catalyst, 2 mL DCM, 50 bar H2, 16 h, rt. Isomerically pure starting materials were evaluated on 0.05 mmol scale in 1 mL DCM and conversion was determined by 1H NMR spectroscopy. Enantiomeric excess was determined by SFC or GC analysis, using chiral stationary phases. DCM dichloromethane, rt room temperature, COD 1,5-cyclooctadiene, BArF tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, conv. conversion.

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