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1,3-dipolar cycloaddition reactions of 1-aryl-N-methyl-2(1H-azol-1-yl)-ethanimineN-oxides to olefins
Autor:
Vassil St. Georgiev, David M. Marinyak, G. A. Bennett, G. B. Mullen, Peter G. Dormer, P. A. Swift
Publikováno v:
Liebigs Annalen der Chemie. 1990:105-107
The regio- and stereoselectivity of the 1,3-dipolar cycloaddition reaction of 1-aryl-N-methyl-2-(1H-azol-1-yl)ethanimine N-oxides 6 to monosubstituted olefins 7 were investigated. The reaction is regioselective, leading to the corresponding C-5 subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07e503fb35fc178a0becfeef77fb532c
https://doi.org/10.1002/jlac.199019900116
https://doi.org/10.1002/jlac.199019900116
