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- Enables sensing of very challenging chiral targets
- Unmatched sensing scope and utility are demonstrated with alcohols having alpha, beta, theta or even gamma stereocenters and with an alcohol chiral by virtue of isotopic substitution
- The reaction sequence enables in-tandem determination of the enantiomeric ratio and concentration of alcohol samples by using readily available chemicals that produce strong chiroptical signals at long wavelengths
OVERVIEW
This Georgetown University invention is a reaction-based chiroptical sensing assay that can detect both the concentration and one or both of the absolute configuration of the chiral alcohol in the sample and enantiomeric purity of various chiral alcohols (alpha, beta, theta, gamma) including those with various stereocenters or by the nature of isotopic substitution. This innovation replaces the need for time-consuming sample work-up and one-at-a-time sample processing. This method increases sample preparation speed, and sample processing, and reduces chemical waste.
BACKGROUND
The technique outperforms the current practice of using alcohol moiety to bind to the sensor. This new method allows for enantio-differentiation for challenging and very specific targets exhibiting remote stereocenters or cryptochirality. The kit offers advantages compared to the current methods as it does not require sample work-up and thus increases production speed. With the recent development of UV/CD plate readers for commercial applications, this innovation sets the groundwork for future advancements in high-throughput compound screening.
Benefit
Market Application
Publications
Provisional patent application filed
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