Publication Details (including relevant citation information):
A.Pignatti, D.Giribone, C.Felicini, E.Fontana
Journal of Labelled Compounds and Radiopharmaceuticals, 46 (2003) 605-611
JTT-501 specifically labelled with 13C was obtained via a four-step synthesis at an isotopic enrichment level of 99% and in 14% overall chemical yield starting from 4-hydroxy-[ring-U-13C6]benzaldehyde (3). The hydrogenation of [13C6]JTT-501 over Pd/C gave [13C6]JTP-20604 in 90% chemical yield.
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