The loss of a methyl radical and the retro diels—Alder reaction in the electron impact mass spectrometry of 2-cyclohexen-1-ol and related compounds

1979 ◽  
Vol 14 (11) ◽  
pp. 609-617 ◽  
Author(s):  
Deniel Braem ◽  
Fazil O. Gülaçar ◽  
Ulrich Burger ◽  
Armand Buchs
1982 ◽  
Vol 17 (2) ◽  
pp. 102-106 ◽  
Author(s):  
Daniel Braem ◽  
Samuel Siles ◽  
Fazil O. Gülaçar ◽  
Armand Buchs

1984 ◽  
Vol 62 (4) ◽  
pp. 655-660 ◽  
Author(s):  
Eric Picquenard ◽  
Jacques Riand ◽  
Jean-Pierre Brun

The fragmentation under electron impact of various methyl-2-pyrimidones is investigated. The fragmentation is markedly influenced by the methyl substituent in the 4- or 5-position and the main fragmentation pathways of the molecular ion involve the loss of carbon monoxide or methyl radical. The latter fragmentation process shows that the methyl groups are more labile in the 4- and(or) 6-position than in the 5-position. This is corroborated by the study of trideuteriomethylated analogues. One can thus distinguish by mass spectrometry the different isomers of position, 4-methyl and 5-methyl or 4,5-dimethyl and 4,6-dimethyl-2-pyrimidones.


1990 ◽  
Vol 27 (5) ◽  
pp. 1293-1295 ◽  
Author(s):  
Elena Ghezzo ◽  
Alberto Sturaro ◽  
Pietro Traldi ◽  
Pierfrancesco Bravo ◽  
Fiorenza Viani

1987 ◽  
Vol 22 (7) ◽  
pp. 462-467 ◽  
Author(s):  
Alberto Sturaro ◽  
Pietro Traldi ◽  
Pierfrancesco Bravo ◽  
Fiorenza Viani ◽  
Giuseppe Resnati

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