Hypervalent Iodine-based Trifluoromethylating Agents Made in Switzerland
DOI:
https://doi.org/10.2533/chimia.2014.419Keywords:
Electrophilic trifluoromethylation, Hypervalent iodine, Structure–reactivity relationshipAbstract
This account aims at providing a general overview over studies carried out in our group on 3,3-dimethyl-1-(trifluoromethyl)-3H-1?3,2-benziodaoxole (1) and 1-(trifluoromethyl)-3H-1?3,2-benziodaoxol-3-one (2). While the first part deals with the syntheses of these increasingly popular reagents, the second part provides in-depth analyses of solid state structures of different derivatives. By means of bond-length derived parameters p changes in the hypervalent bond resulting from backbone modifications could be classified. Furthermore, it is showcased that the parameter p also correlates to solution phase reactivities. Lastly, diverse strategies directed towards the activation of the reagents are exemplified based on selected applications of 1 and 2.Downloads
Published
2014-06-26
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Scientific Articles
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Copyright (c) 2014 Swiss Chemical Society
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
[1]
N. Santschi, A. Togni, Chimia 2014, 68, 419, DOI: 10.2533/chimia.2014.419.