| Literature DB >> 34019429 |
Jeremy R Tuck1, Robert J Tombari1, Noah Yardeny1, David E Olson1,2,3.
Abstract
Azoheteroarenes make up an emerging class of photoswitchable compounds with unique photophysical properties and advantages over traditional azobenzenes. Therefore, methods for synthesizing azoheteroarenes are highly desirable. Here, we utilize azide-alkyne click chemistry to access arylazo-1,2,3-triazoles, a previously unexplored class of azoheteroarenes that exhibit high thermal stabilities and near-quantitative bidirectional photoconversion. Controlling the catalyst or 1,3-dipole grants access to both regioisomeric arylazotriazoles and arylazoisoxazoles, highlighting the versatility of our approach.Entities:
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Year: 2021 PMID: 34019429 PMCID: PMC8276588 DOI: 10.1021/acs.orglett.1c01230
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.072