Zhang, F., Moses, J. E. (April 2009) Benzyne click chemistry with in situ generated aromatic azides. Org Lett, 11 (7). pp. 1587-90. ISSN 1523-7052
DOI: 10.1021/ol9002338
Abstract
An efficient synthesis of substituted benzotriazoles using an azide-alkyne 1,3-dipolar cycloaddition "click reaction" is described. Key to the procedure is the in situ generation of the reactive aromatic azide and benzyne reaction partners.
| Item Type: | Paper |
|---|---|
| Additional Information: | Organic letters |
| Uncontrolled Keywords: | Alkynes/chemistry Azides/chemical synthesis/chemistry Benzene Derivatives/*chemistry Combinatorial Chemistry Techniques Cyclization Molecular Structure Triazoles/*chemical synthesis/chemistry |
| CSHL Authors: | |
| Communities: | CSHL labs > Moses lab |
| Depositing User: | Matthew Dunn |
| Date: | 2 April 2009 |
| Date Deposited: | 19 Apr 2021 20:11 |
| Last Modified: | 19 Apr 2021 20:11 |
| Related URLs: | |
| URI: | https://repository.cshl.edu/id/eprint/39538 |
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