Abstract
The mass spectra of six 1,3,2-oxazaphospholanes have been obtained. The compounds studied give strong m/e=M lines; the relative stability of the molecular ion correlates with the structure of the molecule. During the process of dissociative ionization, cleavage of the C-C and the P-O bonds in the ring takes place, with the molecular ion losing a R'CHO molecule. It has been shown that the molecule of an olefin is formed from the molecular ion mainly through an alkoxy group. A probable process of dissociative ionization is the loss by the molecular ion of an alkoxy group or, in the case of the 2-chloro derivative, the loss of a Cl atom.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 894–897, July, 1973.
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Efremov, Y.Y., Musin, R.Z., Pudovik, M.A. et al. The mass spectra of some 1,3,2-oxazaphospholanes. Chem Heterocycl Compd 9, 824–826 (1973). https://doi.org/10.1007/BF00471558
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DOI: https://doi.org/10.1007/BF00471558