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(TfNNN)-N-15: A gamma-N-15-Labeled Diazo-Transfer Reagent for the Synthesis of beta-N-15-Labeled Azides

Authors
Kwon, Hyeok-JunGwak, SungdukPark, Jun YoungCho, MinhaengHan, Hogyu
Issue Date
1월-2022
Publisher
AMER CHEMICAL SOC
Citation
ACS OMEGA, v.7, no.1, pp.293 - 298
Indexed
SCIE
SCOPUS
Journal Title
ACS OMEGA
Volume
7
Number
1
Start Page
293
End Page
298
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/140194
DOI
10.1021/acsomega.1c04679
ISSN
2470-1343
Abstract
Azides are infrared (IR) probes that are important for structure and dynamics studies of proteins. However, they often display complex IR spectra owing to Fermi resonances and multiple conformers. Isotopic substitution of azides weakens the Fermi resonance, allowing more accurate IR spectral analysis. Site-specifically N-15-labeled aromatic azides, but not aliphatic azides, are synthesized through nitrosation. Both N-15-labeled aromatic and aliphatic azides are synthesized through nucleophilic substitution or diazo-transfer reaction but as an isotopomeric mixture. We present the synthesis of (TfNNN)-N-15, a gamma-N-15-labeled diazo-transfer reagent, and its use to prepare beta-N-15-labeled aliphatic as well as aromatic azides.
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