29788-20-3Relevant academic research and scientific papers
UNUSUAL REACTION OF NITROSO COMPOUNDS WITH THE BIS(AMINOOXY)METHANE/DIBROMOISOCYANURATE SYSTEM
Smirnov, G. A.,Vasil'ev, A. M.,Luk'yanov, O. A.
, p. 2523 - 2524 (1991)
The reaction of nitroso compounds with bis(aminooxy)methane in the presence of dibromoisocyanurate gives the products of the formal replacement of the nitroso group by bromine.
Synthesis of β-nitro ketones from geminal bromonitroalkanes and silyl enol ethers by visible light photoredox catalysis
Cao, Haoying,Ma, Shanshan,Feng, Yanhong,Guo, Yawen,Jiao, Peng
supporting information, p. 1780 - 1783 (2022/02/17)
Various β-nitro ketones, including those bearing a β-tertiary carbon, were prepared from geminal bromonitroalkanes and trimethylsilyl enol ethers of a broad range of ketones by visible light photoredox catalysis, which were then easily converted into β-amino ketones, 1,3-amino alcohols, α,β-unsaturated ketones, β-cyano ketones and γ-nitro ketones.
Electrooxidative coupling of salts of nitro compounds with halide, nitrite, cyanide, and phenylsulfinate anions
Ilovaisky,Merkulova,Ogibin,Nikishin
, p. 1585 - 1592 (2007/10/03)
Electrolysis of salts of primary and secondary nitro compounds (nitroethane, 1- and 2-nitropropanes, nitrocyclohexane, and nitrocycloheptane) in the presence of excess halide, nitrite, cyanide, and phenylsulfinate anions under undivided and divided amperostatic electrolysis conditions in a two-phase medium (CH2Cl2/H2O) produces geminal nitrohalides (35-85% yields), dinitro compounds (15-51%), nitronitriles (6-27%), and nitrosulfones (50-70%). The salts of secondary nitro compounds form the products of oxidative coupling with halide and phenylsulfinate anions under the undivided electrolysis conditions. In all other cases, divided electrolysis is required.
A new method for the one-step conversion of oximes into gem-halo-nitro derivatives
Curini, Massimo,Epifano, Francesco,Marcotullio, Maria Carla,Rosati, Ornelio,Rossi, Monia
, p. 6211 - 6218 (2007/10/03)
A mild and efficient process for one-step conversion of oximes into gem- halo-nitro compounds using Oxone and sodium chloride or potassium bromide is described.
Transformations of Cyclohexanone Oxime into gem-Dinitrocyclohexane
Moiseev,Nafikov,Makarova
, p. 607 - 608 (2007/10/03)
In reaction of cyclohexanone oxime with various electrophilic agents, the highest yields of gem-dinitrocyclohexane were obtained with N2O5 and O3 as oxidants and HNO3 in (CH3CO)2O as a nitrating agent.
New Reagents for the Synthesis of gem-Halonitro Compounds from Oximes
Walters, Thomas R.,Zajac, Walter W.,Woods, James M.
, p. 316 - 321 (2007/10/02)
The utility of the N-haloheterocycles 1-sodio-3,5-dichloro-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (4), 1,3,5-trichloro-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (5), 1,3-dibromo-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (6), and 1,3-dibromo-5,5-dimethylhydantoin (
