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• 3638-64-0 1-nitroethylene 
• 106-99-0 buta-1,3-diene 
• 18942-89-7 2-nitroethyl acetate 
• 110-83-8 cyclohexene 
• 108-24-7 acetic anhydride 
• 4749-28-4 2-nitropropene 
• 1730-25-2 allylmagnesium bromide 
• 609-31-4 2-nitro-1-butanol 

Relevant academic research and scientific papers

ω-Alkenyl α-Nitroalkyl Radicals. Part 3. Radical Chain Reactions of ω-Alkenyl α-Halogenonitroalkanes

SRN1 reactions between 5-bromo-5-nitrohex-1-ene and the nitronate anions of 2-nitropropane and 5-nitrohex-1-ene failed to give cyclisation of the intermediate α-nitroalkyl radical onto the alkene.Reaction between exo-5-bromo-endo-5-nitro-exo-6-phenylbicyclohept-2-ene 1 and the anion of 2-nitropropane did not undergo an SRN1 reaction and Br+ abstraction gave 2-bromo-2-nitropropane and 5-endo-nitro-exo-6-phenylbicyclohept-2-ene.BNAH reduction of exo-5-bromo-endo-5-nitro-exo-6-phenylbicyclohept-2-ene 1, 6-bromo-6-nitrohept-1-ene, and 1-bromo-1-nitro-2-(prop-2-enyl)cyclohexane gave the corresponding nitroalkanes without any cyclosation of the intermediate α-nitroalkyl radicals.Initial results indicate that an iodine atom transfer methodology provides a possible general method for the cylisation of ω-alkenyl α-nitroalkyl radicals.Cyclisation of intermediate α-nitroalkyl radicals, generated by photolysis of 1-(bicyclohept-5-en-endo-2-yl)-2-iodo-2-nitropropane 5a, gave a good yield of two diastereomeric tricyclic iodonitro compounds 6a and 7a.Photolysis of 1-(bicyclohept-5-en-endo-2-yl)-2-iodo-2-nitroethane 5b and 2-(but-3-enyl)-1-iodo-1-nitrocyclohexane 11 also gave the expected products from 5-exo cyclisation of the intermediate α-nitroalkyl radicals.The tricyclic iodonitro compound 6a was synthesised from the corresponding endo-methanesulfonate 15, the structure of which was determined by X-ray crystallography.

Process for the preparation of nitroolefins

A process for the preparation of nitroolefins which comprises heating a solution of a nitroalcohol of the formula: STR1 to at least 125° C. to give a corresponding nitroolefin which is contacted in situ with nucleophilic addition reagent.

Lithium Perchlorate as a Reagent for Synthesis of Covalently Bonded Organic Perchlorates via Electrophilic Additions of Halogens and Nitronium Tetrafluoroborate to Olefins

The reaction of a series of olefins with chlorine and bromine in the presence of a large excess of lithium perchlorate in ether gave 1,2-halo perchlorates together with the corresponding 1,2-dihalides.Analogous reactions of NO2BF4 in methylene chloride or ethyl acetate with monoolefins gave 1,2-nitro perchlorates.Norbornadiene reacted with a NO2BF4/LiClO4 system to give two isomeric nitro perchlorates of nortricyclenic structure.Several synthetic and mechanistic aspects of this new reaction of electrophilic perchloration of olefins are discussed.