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Chemistry of Heterocyclic Compounds
Article . 1987 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
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Mass spectroscopic study of 9-amino- and 9-alkyl(dialkyl, spiro)-1-and 4-azafluorenes

Authors: Zakharov P.I.; Shalimov V.P.; Krokhin A.V.; Prostakov N.S.; Montenegro Kordova G.B.;

Mass spectroscopic study of 9-amino- and 9-alkyl(dialkyl, spiro)-1-and 4-azafluorenes

Abstract

Elimination of a substituent from the 9-position appears to be the main pathway for decomposition of 9-amino-4-azafluorenes. An amine type fragmentation pattern has been observed as well. Decomposition of 9-spiro-4-azafluorenes occurs via cleavage of the radical bound to the three-membered ring. 9-Alkyl-(dialkyl)-1- and 4-azafluorenes also readily lose a substituent in position 9. The observed pathways and principles allow one to determine the nature of the substituent in the 9-position and also to differentiate 1-azafluorenes from 4-azafluorenes. © 1988 Plenum Publishing Corporation.

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Russian Federation
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570, 540

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
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