Abstract
A chiral ferrocene-based boronic acid interacts with (R)- and (S)-Binol to form two complexes that exhibit significantly different. ferrocene-based electrode potentials. This difference in redox behavior can be exploited to demonstrate in principle how high levels of enantiomeric excess in a mixture of enantiomers can be quantified and read-out using an electrochemical method.
Original language | English |
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Pages (from-to) | 8903-+ |
Journal | Journal of the American Chemical Society |
Volume | 132 |
Issue number | 26 |
DOIs | |
Publication status | Published - 1 Jul 2010 |