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Synthesis of a library of 2-aryl-2H-tetrazole-5-carboxamides for photoaffinity labeling of aminergic G-protein coupled receptors. / Zhukovsky, Daniil; Kanov, Evgeny; Gainetdinov, Raul; Krasavin, Mikhail.
в: Mendeleev Communications , Том 32, № 5, 2022, стр. 604-605.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Synthesis of a library of 2-aryl-2H-tetrazole-5-carboxamides for photoaffinity labeling of aminergic G-protein coupled receptors
AU - Zhukovsky, Daniil
AU - Kanov, Evgeny
AU - Gainetdinov, Raul
AU - Krasavin, Mikhail
N1 - Publisher Copyright: © 2022
PY - 2022
Y1 - 2022
N2 - A four-step approach to 2-aryl-2H-tetrazole-5-carboxamides bearing GPCR-focused N-substituted piperazine residues involves ‘SAFE’ diazotransfer onto 1-(piperazin-1-yl)butane-1,3-diones followed by [3+2] cycloaddition of arenediazonium cations at the intermediate ααα-diazo acetamides. The compounds prepared are intended for photoaffinity labeling of aminergic G-protein coupled receptors.
AB - A four-step approach to 2-aryl-2H-tetrazole-5-carboxamides bearing GPCR-focused N-substituted piperazine residues involves ‘SAFE’ diazotransfer onto 1-(piperazin-1-yl)butane-1,3-diones followed by [3+2] cycloaddition of arenediazonium cations at the intermediate ααα-diazo acetamides. The compounds prepared are intended for photoaffinity labeling of aminergic G-protein coupled receptors.
KW - GPCR privileged ligands
KW - photoaffinity labeling
KW - silver(t) catalysis
KW - tetrazoles
KW - [3+2] cycloaddition
KW - α-diazo acetamides
UR - http://www.scopus.com/inward/record.url?scp=85139333311&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/c78a571f-5bc8-34e6-8165-7626a9a4689a/
U2 - 10.1016/j.mencom.2022.09.011
DO - 10.1016/j.mencom.2022.09.011
M3 - Article
AN - SCOPUS:85139333311
VL - 32
SP - 604
EP - 605
JO - Mendeleev Communications
JF - Mendeleev Communications
SN - 0959-9436
IS - 5
ER -
ID: 100361291