Anionic migration reactions in aromatic systems effected by collisional activation : Deprotonated anilides containing methoxycarbonyl substituents


Autoria(s): Blanksby, Stephen J.; Dua, S.; Christie, H.; Bowie, J. H.
Data(s)

04/12/1998

Resumo

Long-range cross-ring reactions are of minor importance in the collision-induced mass spectra (MS/MS) of [M - H]- ions of CH2OCO-C6H4-NHCOR systems: e.g. the loss of 'CD3CO2CH3' from CH3OCO-C6H4-(N) over bar COCD3. Major processes involve (i) losses of radicals to form stable radical anions, e.g. loss of a ring hydrogen atom and losses from the ester (CH3 ., CH3O . and . CO2CH3), (ii) losses of neutral molecules from the amide moiety [e.g. CO (R = H) and CH2CO (R = CH3), and proximity effects when the two substituents are ortho [e.g. loss of (CH3OD+CO2) from o-CH3OCO-C6H4 (N) over bar COCD3].

Identificador

http://eprints.qut.edu.au/70222/

Publicador

John Wiley & Sons Ltd.

Relação

http://onlinelibrary.wiley.com/doi/10.1002/(SICI)1097-0231(19960315)10:4%3C478::AID-RCM514%3E3.0.CO;2-A/pdf

DOI:10.1002/(SICI)1097-0231(19960315)10:4<478::AID-RCM514>3.0.CO;2-A

Blanksby, Stephen J., Dua, S., Christie, H., & Bowie, J. H. (1998) Anionic migration reactions in aromatic systems effected by collisional activation : Deprotonated anilides containing methoxycarbonyl substituents. Rapid Communications in Mass Spectrometry, 10(4), pp. 478-480.

Direitos

Copyright 1996 John Wiley & Sons, Ltd.

Fonte

School of Civil Engineering & Built Environment; Faculty of Science and Technology

Palavras-Chave #induced dissociations #hydrogen
Tipo

Journal Article