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 |
|---|---|
| Pages (from-to) | 8903-8905 |
| Number of pages | 3 |
| Journal | Journal of the American Chemical Society |
| Volume | 132 |
| Issue number | 26 |
| Early online date | 9 Jun 2010 |
| DOIs | |
| Publication status | Published - 7 Jul 2010 |
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