Efficient Synthesis of ω‐[18F]Fluoroaliphatic Carboxylic Esters and Acids for Positron Emission Tomography

Xehetasun bibliografikoak
Parent link:	European Journal of Organic Chemistry Vol. 2020, iss. 40.— 2020.— [P. 6375-6381]
Beste egile batzuk:	Larkina M. S. Mariya Sergeevna, Ozerskaya A. V. Anastasiya Vitaljevna, Podrezova E. V. Ekaterina Vladimirovna, Belousov M. V. Mikhail Valerievich, Tolmachev V. M. Vladimir Maksimilianovich, Zhdankin V. V. Viktor Vladimirovich, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich)
Gaia:	Title screen The important PET tracers, ω‐[18F]fluoroaliphatic carboxylic acid derivatives, were prepared by nucleophilic radiofluorination of the readily available iodocarboxylic esters. Methyl 6‐[18F]fluorohexanoate was further applied as a starting material for the preparation of the succinimide ester (NHS ester)‐containing bifunctional radiofluorinated prosthetic group in two simple steps, 10 min each.
Hizkuntza:	ingelesa
Argitaratua:	2020
Gaiak:	электронный ресурс труды учёных ТПУ fluorinated compounds isotopes PET radiotracers radiofluorination synthetic methods фторирование изотопы синтетические методы
Sarrera elektronikoa:	https://doi.org/10.1002/ejoc.202000934
Formatua:	Baliabide elektronikoa Liburu kapitulua
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=663735

Deskribapena
Gaia:	Title screen The important PET tracers, ω‐[18F]fluoroaliphatic carboxylic acid derivatives, were prepared by nucleophilic radiofluorination of the readily available iodocarboxylic esters. Methyl 6‐[18F]fluorohexanoate was further applied as a starting material for the preparation of the succinimide ester (NHS ester)‐containing bifunctional radiofluorinated prosthetic group in two simple steps, 10 min each.
DOI:	10.1002/ejoc.202000934

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