Reactivity of ferrocenylalkylazoles under conditions of dissociative ionization View Full Text


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Article Info

DATE

2005-10

AUTHORS

Yu. S. Nekrasov, R. S. Skazov, A. A. Simenel, L. V. Snegur, V. V. Gumenyuk

ABSTRACT

Electron ionization mass spectra of biologically active ferrocenylalkylazoles CpFeC5H4CH(R)Az (R = H, Me, Et, Pr, or Ph; AzH is pyrazole, imidazole, indazole, benzoimidazole, benzotriazole, adenine, or their derivatives) were studied. The nature of the heterocyclic fragment (its ionization energy) is the main factor determining the reactivity of these compounds under conditions of dissociative electron ionization. More... »

PAGES

2460-2462

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-006-0138-x

DOI

http://dx.doi.org/10.1007/s11172-006-0138-x

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1007606084


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