Orientation of dinitrogen trioxide addition to 2-methylpropene and structure of the addition product
作者:Josef Pfab
DOI:10.1039/c39770000766
日期:——
The structure of the crystalline addition product of dinitrogentrioxide to 2-methylpropene is established unequivocally as trans-2-methyl-2-nitroso-1-nitropropane dimer indicating that the addition proceeds at least partially if not predominantly by a radical mechanism.
Gowenlock, Brian G.; King, Boyd; Pfab, Josef, Journal of the Chemical Society. Perkin Transactions 2 (2001), 1998, # 3, p. 483 - 485
作者:Gowenlock, Brian G.、King, Boyd、Pfab, Josef、Witanowski, Michal
DOI:——
日期:——
Reaction of dinitrogen trioxide with 2-methylpropene and other alkenes. Evidence for electrophilic nitrosation
作者:James R. Park、D. Lyn H. Williams
DOI:10.1039/p29760000828
日期:——
solid dimer product from the reaction of dinitrogentrioxide and 2-methylpropene was converted to the corresponding oxime by heating with or without a solvent for ca. 2 days. This establishes the orientation of the dinitrogentrioxide addition product as the 1-nitroso- rather than the 2-nitroso-compound as previously thought. A number of other alkene–dinitrogen trioxide adducts have been prepared; most