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Citation
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HERO ID
5348652
Reference Type
Journal Article
Title
Nonafluoro- tert-butoxylation of Diaryliodonium Salts
Author(s)
Meng, H; Wen, L; Xu, Z; Li, Y; Hao, J; Zhao, Y
Year
2019
Is Peer Reviewed?
1
Journal
Organic Letters
ISSN:
1523-7060
EISSN:
1523-7052
Volume
21
Issue
13
Page Numbers
5206-5210
Language
English
PMID
31247748
DOI
10.1021/acs.orglett.9b01813
Abstract
A highly efficient method to incorporate the nonafluoro- tert-butoxy group into various arenes is developed. This C-O cross-coupling reaction proceeds smoothly in the absence of transition-metal catalyst with good functional group tolerance and scalability. In comparison with the conventional approach, this method avoids the use of nonafluoro- tert-butyl alcohol as the reaction solvent and does not require handling of hazardous diazonium salts. A series of OC(CF3)3-containing analogues of 19F NMR-based probes targeting various biologically relevant analytes are prepared.
Tags
IRIS
•
tert-Butanol
Excluded/ Not on Topic
Chemical Analysis/Fuel Chemistry
LitSearch: Jan 2017 - July 2019
PubMed
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