Synthesis and Mass Spectral Fragmentation Patterns of Brassinolide Early Biosynthetic Precursors Labeled at C-26
2013 ◽
Vol 8
(6)
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pp. 1934578X1300800
Keyword(s):
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.
1994 ◽
Vol 23
(9)
◽
pp. 540-546
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1973 ◽
Vol 28
(11-12)
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pp. 820-823
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1973 ◽
Vol 28
(11-12)
◽
pp. 646-649
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Keyword(s):
2016 ◽
Vol 88
(23)
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pp. 11624-11630
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1994 ◽
Vol 5
(7)
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pp. 655-675
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2016 ◽
Vol 12
(5)
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pp. 439-449
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