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Daughter ion mass spectra of 11-pentafluorobenzyl ester derivatives of 11-dehydiothromboxane B2 and B3

✍ Scribed by Aldo Ferretti; Vincent P. Flanagan


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
281 KB
Volume
27
Category
Article
ISSN
1076-5174

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✦ Synopsis


Collisionally activated decomposition (CAD) mass spectra of the [ M -C,F,CH,'Iions of 1-methyl ester-1 1pentafluorobenzyl ester-9,12,15-tris(trimethylsilyI) and 9,12,15-tris(ethyldimethylsilyl) ether derivatives of 11dehydrothromboxane B, are presented and discussed. The spectra are interpreted with the aid of those of a corresponding 3,3,4,4tetradeutero compound and of an analogous derivative of 1 ldehydrothromboxane B, . Proposed fragmentation pathways are based on internal consistency of data from all four compounds. The migration of a trimethylsilyl or an ethyldimethylsilyl group is the salient feature of all the CAD spectra.


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## Abstract Aza Wittig reaction of bis(iminophosphorane) 3 with two equivalents of aryl isocyanates directly provided the bicyclic guanidines 4. However, 3 undergoes intramolecular aza Wittig reaction on thermal treatment to give the iminophosphorane 6 derived from the 2‐(__o__‐azidophenyl)‐4(3__H_