The addition reaction of α‐azido ethers and α‐azido thioethers to phenylacetylene

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Abstract
Several v‐triazoles were synthesized by 1,3‐dipolar cycloaddition of certain α‐azido ethers and α‐azidothioethers to phenylacetylene. In most of the cases the reaction led to the formation of the two isomeric v‐triazoles. Structural assignments for the products obtained were made on the basis of NMR data and chemical reactions. Characteristic differences between the NMR spectra of the isomers have been noted.

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