Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Viktoriya Orlovskaya"'
Publikováno v:
European Journal of Organic Chemistry. 2020:7079-7086
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::734fcf863bc7cd7c901253f9559c83b1
https://doi.org/10.1002/ejoc.202001198
https://doi.org/10.1002/ejoc.202001198
Publikováno v:
Radiochimica Acta. 108:979-988
The 16α-[18F]Fluoroestradiol ([18F]FES) is an established PET radiotracer for estrogen positive (ER+) breast cancer. Although the radiosynthesis is well-described, the majority of the published methods suffer from modest or irreproducible yields and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd90b624f50807cee0ca6797f58ca0ea
https://doi.org/10.1515/ract-2020-0058
https://doi.org/10.1515/ract-2020-0058
Autor:
Bernd Neumaier, O. F. Kuznetsova, Boris D. Zlatopolskiy, Viktoriya Orlovskaya, Austin Craig, Olga S. Fedorova, Raisa Krasikova
Publikováno v:
Molecules
Volume 26
Issue 18
Molecules 26(18), 5550 (2021). doi:10.3390/molecules26185550
Molecules, Vol 26, Iss 5550, p 5550 (2021)
Volume 26
Issue 18
Molecules 26(18), 5550 (2021). doi:10.3390/molecules26185550
Molecules, Vol 26, Iss 5550, p 5550 (2021)
6-l-[18F]Fluoro-m-tyrosine (6-l-[18F]FMT) represents a valuable alternative to 6-l-[18F]FDOPA which is conventionally used for the diagnosis and staging of Parkinson’s disease. However, clinical applications of 6-l-[18F]FMT have been limited by the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcc395c230a1688f33f4902b34d89b8d
Autor:
Viktoriya, Orlovskaya, Dmitrii, Antuganov, Olga, Fedorova, Vasilii, Timofeev, Raisa, Krasikova
Publikováno v:
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine. 163
Here we describe use of the tetrabutylammonium p-toluenesulfonate (TBAOTs) as an inert phase transfer catalyst allowing high efficient aliphatic radiofluorination of labeling precursors for the preparation of common radiotracers using only 0.2-1.2 mg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::92b1f25d9c9e259c04a7be5f03253c31
https://pubmed.ncbi.nlm.nih.gov/32561038
https://pubmed.ncbi.nlm.nih.gov/32561038
Publikováno v:
Applied Radiation and Isotopes. 163:109195
Here we describe use of the tetrabutylammonium p-toluenesulfonate (TBAOTs) as an inert phase transfer catalyst allowing high efficient aliphatic radiofluorination of labeling precursors for the preparation of common radiotracers using only 0.2–1.2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::147f1455d0daa212504017b62226c8af
https://doi.org/10.1016/j.apradiso.2020.109195
https://doi.org/10.1016/j.apradiso.2020.109195
Publikováno v:
Russian Chemical Bulletin. 64:1518-1535
Potential of electrophilic and nucleophilic methods of radiofluorination in the synthesis of fluorine-18-labeled fluorinated amino acid analogs, radiotracers for positron emission tomography (PET), is considered. The synthesis of 6-L-[18F]FDOPA ((S)-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::789d521f7119349a3e71120d851fea17
https://doi.org/10.1007/s11172-015-1037-9
https://doi.org/10.1007/s11172-015-1037-9
Autor:
Raisa Krasikova, Ch. V. Chang, Viktoriya Orlovskaya, Ch. L. Chen, Yu. N. Belokon, R. Sh. Liu, T. F. Savel'eva, Olga S. Fedorova, Victor I. Maleev
Publikováno v:
Russian Chemical Bulletin. 63:1169-1177
An asymmetric synthesis method has been suggested as a feasible approach for the preparation of fluorine-18-labeled (T1/2 110 min) analog of l-threo-3,4-dihydroxyphenylserine, i.e., 6-l-threo-[18F]FDOPS ((2S,3R)-2-amino-3-(2-[18F]fluoro-4,5-dihydroxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::234fb89664fb6f909f89039697abf6cc
https://doi.org/10.1007/s11172-014-0567-x
https://doi.org/10.1007/s11172-014-0567-x