Organic mass spectrometry

Mass spectra of dicyanomethylene derivatives of benzophenone analogs

CB Wang, GR Her, JT Watson

Index: Wang, Ching-Bore; Her, Guor-Rong; Watson, J. Throck Organic Mass Spectrometry, 1983 , vol. 18, # 10 p. 457 - 461

Full Text: HTML

Citation Number: 3

Abstract

Abstract The dicyanomethylene derivative of a benzophenone analog significantly alters the fragmentation pattern observed during electron impact ionization of the underivatized parent compound. A double bond connecting the dicyanomethylene moiety to the parent compound is cleaved during a major fragmentation pathway for many of these compounds. A mechanism involving rearrangement of two hydrogen atoms is proposed to rationalize ...

Related Articles:

Silver (I) Ion-Mediated Desulfurization-Condensation of Thiocarbonyl Compounds with Several Nucleophiles.

[Shibuya, Isao; Taguchi, Yoichi; Tsuchiya, Tohru; Oishi, Akihiro; Katoh, Eisaku Bulletin of the Chemical Society of Japan, 1994 , vol. 67, # 11 p. 3048 - 3052]

More Articles...