Benzyne click chemistry with in situ generated aromatic azides

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

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:	Moses, John E.
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:	Publisher
URI:	https://repository.cshl.edu/id/eprint/39538

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