ADDITION REACTION OF ALPHA-AZIDO ETHERS AND ALPHA-AZIDO THIOETHERS TO PHENYLACETYLENE

被引:21
作者
GARCIAMUNOZ, G
MADRONER.R
RICO, M
SALDANA, MC
机构
[1] Instituto de Quimica Orgánica General, Departamento de Quimica Médica, Madrid
关键词
D O I
10.1002/jhet.5570060624
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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. Copyright © 1969 Journal of Heterocyclic Chemistry
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页码:921 / +
页数:1
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