Reaction mechanism of gaseous organic cations-21. Skeletal rearrangement of ionized N-aryl-3,4-diphenylisoxazol-5(2H)-one

Ionized N-aryl-3,4-diphenylisoxazol-5(2H)-one isomers react unimolecularly in the gas-phase mainly via carbon dioxide elimination. The observed ring contraction closely resembles the reported behaviour of the corresponding neutral compounds in solution. The reacting species were produced by electron impact (EI) and field ionization (FI) and analyzed by MS/MS through the determination of specific metastable ions (MI) decompositions.

Reaction mechanism of gaseous organic cations-21. Skeletal rearrangement of ionized N-aryl-3,4-diphenylisoxazol-5(2H)-one / Liguori, Angelo; Sindona, Giovanni; Uccella, N.. - In: TETRAHEDRON. - ISSN 0040-4020. - 40:5(1984), pp. 925-929.



Titolo: Reaction mechanism of gaseous organic cations-21. Skeletal rearrangement of ionized N-aryl-3,4-diphenylisoxazol-5(2H)-one
Autori: 
LIGUORI, Angelo
SINDONA, Giovanni
mostra contributor esterni 
Data di pubblicazione: 1984
Rivista: 
TETRAHEDRON  
Citazione: Reaction mechanism of gaseous organic cations-21. Skeletal rearrangement of ionized N-aryl-3,4-diphenylisoxazol-5(2H)-one / Liguori, Angelo; Sindona, Giovanni; Uccella, N.. - In: TETRAHEDRON. - ISSN 0040-4020. - 40:5(1984), pp. 925-929.
Handle: http://hdl.handle.net/20.500.11770/143125
Appare nelle tipologie:1.1 Articolo in rivista

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