A scalable and versatile methodology for production of vinylated carboxylic compounds with (13) C isotopic label in C1 position is described. It allowed synthesis of vinyl acetate-1-(13) C, which is a precursor for preparation of (13) C hyperpolarized ethyl acetate-1-(13) C, which provides a convenient vehicle for potential in vivo delivery of hyperpolarized acetate to probe metabolism in living organisms. Kinetics of vinyl acetate molecular hydrogenation and polarization transfer from para-hydrogen to (13) C via magnetic field cycling were investigated. Nascent proton nuclear spin polarization (%PH ) of ca. 3.3 % and carbon-13 polarization (%P13C ) of ca. 1.8 % were achieved in ethyl acetate utilizing 50 % para-hydrogen corresponding to ca. 50 % polarization transfer efficiency. The use of nearly 100% para-hydrogen and the improvements of %PH of para-hydrogen-nascent protons may enable production of (13) C hyperpolarized contrast agents with %P13C of 20-50 % in seconds using this chemistry.
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http://dx.doi.org/10.1002/anie.201600521 | DOI Listing |
Chemistry
November 2016
Department of Radiology, Department of Biomedical Engineering, Department of Physics and Astronomy, Vanderbilt University Institute of Imaging Science (VUIIS), Nashville, Tennessee, 37232-2310, USA.
A supported metal catalyst was designed, characterized, and tested for aqueous phase heterogeneous hydrogenation of vinyl acetate with parahydrogen to produce C-hyperpolarized ethyl acetate for potential biomedical applications. The Rh/TiO catalyst with a metal loading of 23.2 wt % produced strongly hyperpolarized C-enriched ethyl acetate-1- C detected at 9.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
May 2016
Department of Radiology, Vanderbilt University Institute of Imaging Science (VUIIS), Department of Biomedical Engineering, Vanderbilt-Ingram Cancer Center (VICC), Vanderbilt University, Nashville, TN, 37232, USA.
A scalable and versatile methodology for production of vinylated carboxylic compounds with (13) C isotopic label in C1 position is described. It allowed synthesis of vinyl acetate-1-(13) C, which is a precursor for preparation of (13) C hyperpolarized ethyl acetate-1-(13) C, which provides a convenient vehicle for potential in vivo delivery of hyperpolarized acetate to probe metabolism in living organisms. Kinetics of vinyl acetate molecular hydrogenation and polarization transfer from para-hydrogen to (13) C via magnetic field cycling were investigated.
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