Authors:
R. Tinková Charles University in Prague Department of Organic and Nuclear Chemistry Hlavova 8 128 40 Praha 2 Czech Republic

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L. Lešetický Charles University in Prague Department of Organic and Nuclear Chemistry Hlavova 8 128 40 Praha 2 Czech Republic

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Abstract  

New (radio)halogen derivatives of 1-allylterguride have been prepared by method of destannylation-halogenation. 1-Alylterguride shows relatively high binding affinity, which can be used in the case of its radiolabeled derivatives with imaging methods like PET or SPET in studies of properties of receptor's binding places and ligand affinity. The (radio)halogenation was performed via organotin precursors: 1-tributylstannyl-3-chlorprop-1-ene and 2-tributylstannyl-3-chloroprop-1-ene, which were prepared from appropriate alcohols. Linkers of the tin group were used for alkylation of N1 of terguride both under microwave irradiation and under conventional heating. In the last step (destannylation-halogenation), fluoro-, bromo- and iododerivatives as well as 125I iodo- and 82Br bromoderivatives of 1-allylterguride were obtained.

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Journal of Radionalytical and Nuclear Chemistry
Language English
Size A4
Year of
Foundation
1968
Volumes
per Year
1
Issues
per Year
12
Founder Akadémiai Kiadó
Founder's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Publisher Akadémiai Kiadó
Springer Nature Switzerland AG
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
CH-6330 Cham, Switzerland Gewerbestrasse 11.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 0236-5731 (Print)
ISSN 1588-2780 (Online)