Chem. J. Chinese Universities ›› 1993, Vol. 14 ›› Issue (4): 508.

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A Study of Mass Spectrometry of 2-Amino-5-substituted-4-thiazolyl Phosphonates

JIAO Xian-Yun, HU Bing-Fang   

  1. Institute of Applied Chemistry, Beijing Agricultrual University, Beijing, 100094
  • Received:1992-05-19 Revised:1992-11-23 Online:1993-04-24 Published:1993-04-24

Abstract: The fragmentation characteristic of a series of recently developed 2-amino-5-substituted-4-thiazolyl-phosphonates is studied by using electron impact (EI), electron impact-collision activity-mass analysed ion kinetic energy spectrometry (EI-CA-MIKES) and accurate mass measurment (AMM) techniques.It is found that a new type of γ-alkyl rearrangement has occured as evidenced by the'pres-ence of a molecular daughter ion of ethylated thiazole ring(m/z 203).The molecular parent and daughter ions have been fully identified by their unsaturation, accurate ion mass and elementary constitution.The fragmentation pathway is portrayed in a scheme(see Fig.2)

Key words: γ-Alkyl rearrangment, EI-CA-MIKES, Thiazolyl, Phosphonate

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