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Mass spectrometry and pyrolytic decomposition of 2-amino-3′,4′,6-trisubstituted isoflavones

✍ Scribed by Peifeng Hu; Yongfu Li; Yongquan Lu; Kalevi Pihlaja


Book ID
102559509
Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
290 KB
Volume
28
Category
Article
ISSN
1076-5174

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✦ Synopsis


The 2-aminoisoflavones studied exhibited some familiar fragmentation pathways, such as the formation of the retro-Diels-Alder ions. However, substitutions at C(2), C(3'), C(4') and C(6) induced some specific decompositions of both mass spectrometric and pyrolytic origin. Pyrolytic decompositions reverse to the Mannich reaction occurred with all compounds to variable extents. The three compounds with the (Me),NSO, substitution at C(6) exhibited another type of pyrolytic reaction, namely the formation of products corresponding to ions of m/z 272, 300 and 314, depending on the type of substitution at C(3'). The occurrence of an interesting 'ortho effect', the elimination of the elements of CH,O from C(3') and C(4'), was also established.


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