Mass spectral fragmentation of trimethylsilyl derivatives of 2-amino-4-hydroxypteridines: A method of identification

1970 ◽  
Vol 37 (2) ◽  
pp. 285-292 ◽  
Author(s):  
Pat Haug
Keyword(s):  
Mass Spectral Fragmentation ◽  
Mass Spectral ◽  
Trimethylsilyl Derivatives ◽  
Derivatives Of

Massenspektrometrische Fragmentierung von Trimethylsilylderivaten (TMS) des Thyrotropin-„Releasing“-Hormons (TRH) und dessen Teilstrukturen / Mass Spectroscopy of Trimethylsilyl Derivatives of Thyrotropin-releasing Hormone and its Constituents

1973 ◽  
Vol 28 (11-12) ◽  
pp. 820-823 ◽  
Author(s):  
W. A. König ◽  
S. Fuchs ◽  
K. Zech ◽  
W. Voelter
Keyword(s):  
Mass Spectrometry ◽  
Mass Spectroscopy ◽  
Peptide Hormones ◽  
Thyrotropin Releasing Hormone ◽  
Mass Spectral Fragmentation ◽  
Releasing Hormone ◽  
Mass Spectral ◽  
Trimethylsilyl Derivatives ◽  
Fragmentation Patterns ◽  
Derivatives Of

The mass spectral fragmentation patterns of trimethylsilyl derivatives of TRH and its constituents are discussed. The utility of these derivatives for the control of the synthesis of peptide hormones by mass spectrometry is obvious.

Synthesis and Identification of ω-Phenylalkylcatechols in Burmese Lac

1988 ◽  
Vol 41 (1) ◽  
pp. 19 ◽  
Author(s):  
A Jefferson ◽  
MV Sargent ◽  
S Wangchareontrakul
Keyword(s):  
Natural Products ◽  
Catalytic Hydrogenation ◽  
Wittig Reaction ◽  
Spectral Characteristics ◽  
Chromatographic Retention ◽  
Phosphonium Bromide ◽  
Mass Spectral ◽  
Trimethylsilyl Derivatives ◽  
Derivatives Of

The presence of 3-(10′-phenyldecyl)-(2) (2%), 3-(12′-phenyldodecyl)- (3) (6%), 4-(10′-phenyldecyl)-(4) (0.3%) and 4-(12′-phenyldodecyl)- benzene-1,2-diol (5) (0.3%) in Burmese lac , the sap of Melanorrhoea usitata Wall has been confirmed by the synthesis of these compounds and a comparison of the gas chromatographic retention times and the mass spectral characteristics of their bis-O-( trimethylsilyl ) derivatives with the derivatives of the natural products. Typically, 3,4- bis ( benzyloxy ) benzaldehyde (7) on Wittig reaction with triphenyl (11- phenylundecyl ) phosphonium bromide (20) and subsequent catalytic hydrogenation of the resultant olefin gave compound (5) in 59% overall yield.

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