Chemical ionization mass spectrometry of macrolide antibiotics. III—M-4365 and related compounds

1981 ◽  
Vol 8 (8) ◽  
pp. 332-336 ◽  
Author(s):  
Makoto Suzuki ◽  
Ken-Ichi Harada ◽  
Naohito Takeda ◽  
Akira Tatematsu
1985 ◽  
Vol 20 (7) ◽  
pp. 435-439 ◽  
Author(s):  
Walter A. Korfmacher ◽  
Claude L. Holder ◽  
James P. Freeman ◽  
Ronald K. Mitchum ◽  
Aubrey B. Gosnell

1975 ◽  
Vol 58 (3) ◽  
pp. 541-547 ◽  
Author(s):  
Roy L Holmstead ◽  
John E Casida

Abstract The chemical ionization (CI) mass spectra with methane as the reagent gas are reported for 25 N-methylcarbamato insecticides or related compounds. The [M + 1]+ ions in the CI spectra are larger than the parent ions in the corresponding electron impact (EI) spectra of N-methyl- and N,N-dimethylcarbamates, but the contrary is true with N-hydroxymethylcarbamates. CI but not EI fragmentation of substituted- phenyl N-hydroxymethylcarbamates [ROC(0)NHCH2OH] appears to involve a 4-membered [ROC(0)NHCH2]+ intermediate which rearranges to give a [ROCH2]+ fragment. Other fragmentations unique to the CI spectra are also discussed.


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