1. Investigation of copper-free alkyne/azide 1,3-dipolar cycloadditions using microwave irradiation.
- Author
-
Chatkewitz LE, Halonski JF, Padilla MS, and Young DD
- Subjects
- Cycloaddition Reaction, Models, Molecular, Molecular Structure, Triazoles chemistry, Alkynes chemistry, Azides chemistry, Microwaves, Triazoles chemical synthesis
- Abstract
The prevalence of 1,3-dipolar cycloadditions of azides and alkynes within both biology and chemistry highlights the utility of these reactions. However, the use of a copper catalyst can be prohibitive to some applications. Consequently, we have optimized a copper-free microwave-assisted reaction to alleviate the necessity for the copper catalyst. A small array of triazoles was prepared to examine the scope of this approach, and the methodology was translated to a protein context through the use of unnatural amino acids to demonstrate one of the first microwave-mediated bioconjugations involving a full length protein., (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Published
- 2018
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