scholarly journals Synthesis and Mass Spectral Fragmentation Patterns of Brassinolide Early Biosynthetic Precursors Labeled at C-26

2013 ◽  
Vol 8 (6) ◽  
pp. 1934578X1300800
Author(s):  
Vladimir A. Khripach ◽  
Danuše Tarkowská ◽  
Vladimir N. Zhabinskii ◽  
Olga V. Gulyakevich ◽  
Yurii V. Ermolovich ◽  
...  

New analogues of brassinolide biosynthetic precursors with three deuterium atoms at non-exchangeable positions have been synthesized to be used as standards for quantification of natural brassinosteroids by liquid chromatography-mass spectrometry. [26-2H3](22 R,23 R,24 S)-22,23-Dihydroxy-6β-methoxy-24-methyl-3α,5-cyclo-5α-cholestane was used as a starting material for the preparation of campestane derivatives having a 22 R,23 R-diol functionality and either a hydroxy or keto group at C-3 and labeled at C-26. The mass spectrometric behavior of the newly synthesized compounds has been studied.

1973 ◽  
Vol 28 (11-12) ◽  
pp. 820-823 ◽  
Author(s):  
W. A. König ◽  
S. Fuchs ◽  
K. Zech ◽  
W. Voelter

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.


1973 ◽  
Vol 28 (11-12) ◽  
pp. 646-649 ◽  
Author(s):  
Krishna C. Joshi ◽  
Lalit Prakash ◽  
R. K. Bansal ◽  
Pahup Singh

Abstract Mass spectral fragmentation studies of dehydro-a-lapachone and dehydro-iso-a-lapadione, isolated from the heartwood of Tabebuia rosea, have been made. The fragmentation patterns in the case of two compounds are essentially similar and have been discussed


2016 ◽  
Vol 12 (5) ◽  
pp. 439-449 ◽  
Author(s):  
Sotirios M. Bratakos ◽  
Vassilia J. Sinanoglou ◽  
Minos T. Matsoukas ◽  
Eleni Siapi ◽  
Demetris P. Papahatjis ◽  
...  

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