Chemical lonization mass spectrometry of trimethylsilyl derivatives of various prostaglandins
β Scribed by Toshio Ariga; Minoru Suzuki; Ikuo Morita; Sei-itsu Murota; Tadashi Miyatake
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- English
- Weight
- 441 KB
- Volume
- 90
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
Methoxime-trimethylsilyl
derivatives of prostaglandin A, B, and E series and trimethylsilyl derivatives of prostaglandin F series were investigated by gas chromatography-chemical ionization (CI) mass spectrometry. In ammonia CI mass spectrometry of both derivatives, the ion at m/e (M + l)+ or (M + 18)+ was recorded as the base peak. The syn and anti isomers of prostaglandin A and E series could be distinguished from each other by a characteristic ion, which was produced by the loss of trimethylsilanol from m/e (M + I)+. The (Y and p isomers of prostaglandin F series could also be discriminated from each other by comparing the intensities of the characteristic ions from sequential loss of trimethylsilanols from m/e (M + l)+ and (M + 18)+.
π SIMILAR VOLUMES
Allyldimethylsilyl ethers of prostaglandin E2 and F, , leukotriene B4 and S@-pregnane3a, 2Oa-diol were prepared at room temperature in good yields with the novel reagent N,O-bis(allyldimethyIsi1yl)-trifluoroacetamide. The gas chromatographic properties of the derivatives of prostaglandins and the st