TY - JOUR
T1 - One-pot synthesis of [11C]ureas via triphenylphosphinimines
AU - Van Tilburg, Erica W.
AU - Windhorst, Albert D.
AU - Van Der Mey, Margreet
AU - Herscheid, Jacobus D.M.
PY - 2006/3/30
Y1 - 2006/3/30
N2 - A series of 11C-labeled ureas was prepared using a rapid and efficient one-pot procedure. First, the intermediate [11C] phenylisocyanate was formed with phenyltriphenylphosphinimine and [ 11C]CO2. A range of amines was then reacted with the [11C]phenylisocyanate yielding the [11C]urea derivatives in short synthesis times. This easy-to-handle method circumvents disadvantages of known procedures and generates the possibility to prepare other kinds of 11C-labeled compounds using a variety of phenylphosphinimines in combination with different nucleophiles. The presented approach is an alternative to the use of established methods in 11C-labeling chemistry.
AB - A series of 11C-labeled ureas was prepared using a rapid and efficient one-pot procedure. First, the intermediate [11C] phenylisocyanate was formed with phenyltriphenylphosphinimine and [ 11C]CO2. A range of amines was then reacted with the [11C]phenylisocyanate yielding the [11C]urea derivatives in short synthesis times. This easy-to-handle method circumvents disadvantages of known procedures and generates the possibility to prepare other kinds of 11C-labeled compounds using a variety of phenylphosphinimines in combination with different nucleophiles. The presented approach is an alternative to the use of established methods in 11C-labeling chemistry.
KW - C-labeled ureas
KW - Phosphinimines
KW - [C]CO
KW - [C]isocyanates
UR - http://www.scopus.com/inward/record.url?scp=33646381357&partnerID=8YFLogxK
U2 - https://doi.org/10.1002/jlcr.1052
DO - https://doi.org/10.1002/jlcr.1052
M3 - Article
SN - 0362-4803
VL - 49
SP - 321
EP - 330
JO - Journal of Labelled Compounds and Radiopharmaceuticals
JF - Journal of Labelled Compounds and Radiopharmaceuticals
IS - 4
ER -