首页 | 本学科首页   官方微博 | 高级检索  
     


Mass-spectrometric study of the cyclization of diazo compounds. 9. 2-Diazo-2-cyanoacetamides
Authors:A. T. Lebedev  P. A. Sharbatyan  A. G. Kazaryan  V. A. Bakulev  Yu. M. Shafran  V. S. Petrosyan
Affiliation:(1) M. V. Lomonosov Moscow State University, 117234 Moscow;(2) The Scientific Research Institute of Organic Intermediates and Dyes, 103787 Moscow;(3) S. M. Kirov Urals Polytechnic Institute, 620002 Sverdlovsk
Abstract:An analysis of the electron impact mass-spectra of 2-diazo-2-cyanoacetamides and the 4-cyano-5-hydroxy-1,2,3-triazoles isomeric to them, showed that the molecular ions of these compounds do not isomerize one into another. The diazo compounds decompose, undergoing a Wolff rearrangement. To study the fragmentation of the diazoamides, one can use the crystalline adducts of these diazo compounds with triphenylphosphine, and to study the fragmentation of the triazoles, their salts with aliphatic amines.See [1] for No. 8 in the series.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1343–1349, October, 1986.
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号