LOW-TEMPERATURE SYNTHESIS OF NO-CARRIER-ADDED [C-11] FORMALDEHYDE WITH METAL-HYDRIDES AND PREPARATION OF [1-C-11]1,2,3,4-TETRAHYDRO-BETA-CARBOLINE DERIVATIVES
Mw. Nader et al., LOW-TEMPERATURE SYNTHESIS OF NO-CARRIER-ADDED [C-11] FORMALDEHYDE WITH METAL-HYDRIDES AND PREPARATION OF [1-C-11]1,2,3,4-TETRAHYDRO-BETA-CARBOLINE DERIVATIVES, Applied radiation and isotopes, 49(12), 1998, pp. 1599-1603
Citations number
18
Categorie Soggetti
Nuclear Sciences & Tecnology","Radiology,Nuclear Medicine & Medical Imaging","Chemistry Inorganic & Nuclear
A comparative study has been performed on the selective reduction of c
yclotron-produced [C-11]carbon dioxide to [C-11]formaldehyde with solu
tions of various complex metal hydrides at temperatures between -52 an
d +25 degrees C. Under optimal reaction conditions, lithium tetrahydri
doaluminate gave the highest yield of [C-11]formaldehyde (58%, decay-c
orrected), followed by lithium triethylhydridoborate (34%) and sodium
tetrahydridoborate (22%). Radiochemically pure [C-11]formaldehyde coul
d be obtained with lithium tetrahydridoaluminate and sodium tetrahydri
doborate, but not with lithium triethyl hydridoborate. The produced [C
-11]formaldehyde was used for the synthesis of [1-C-11]1,2,3,4-tetrahy
dro-beta-carboline derivatives by the Pictet-Spengler reaction. (C) 19
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