The Bücherer-Strecker synthesis of d- and l-(1-11C)tyrosine and the in vivo study of l-(1-11C)tyrosine in human brain using positron emission tomography

Abstract

The synthesis of d-and l-(1-11C)tyrosine, starting with 11C-cyanide, is reported. dl-(1-11C)Tyrosine was prepared by the Bücherer-Strecker reaction, from carrier added 11C-cyanide with an incorporation of 80% in 20 min. The isolation of the pure d- and l-amino acid isomers from the enantiomeric mixture was accomplished within 15 min by preparative HPLC using a chiral stationary phase and a phosphate buffer as the mobile phase. Typically, the total synthesis time was 50 min (including purification) from end of trapping of 11C-cyanide, with a radiochemical yield of d- and l-amino acid of 40%–60%. The d- and l-(1-11C)tyrosine were both obtained optically pure, with a carrier added specific activity of 0.3–0.5 Ci/mmol and a radiochemical purity better than 99%. The 11C labelled l-tyrosine was used in an in vivo study in the human brain using positron emission tomography (PET).

DOI: 10.1007/BF00256552

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@article{Halldin1987TheBS, title={The B{\"{u}cherer-Strecker synthesis of d- and l-(1-11C)tyrosine and the in vivo study of l-(1-11C)tyrosine in human brain using positron emission tomography}, author={Christer Halldin and K. Schoeps and Sharon Stone-Elander and F Wiesel}, journal={European Journal of Nuclear Medicine}, year={1987}, volume={13}, pages={288-291} }