- Synthesis of unsaturated silyl nitronates via the silylation of conjugated nitroalkenes
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A new method for the synthesis of conjugated silyl nitronates from nitroalkenes is described. The procedure has wide substrate scope and is compatible with in situ generation of the substrates from 2-nitroalcohols or 2-chloro-nitroalkanes. A cascade transformation to give 3,4,5,6-tetrahydropyridine N-oxide derivatives was disclosed.
- Khotyantseva, Elizaveta A.,Tabolin, Andrey A.,Novikov, Roman A.,Nelyubina, Yulia V.,Ioffe, Sema L.
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supporting information
p. 3128 - 3131
(2018/07/13)
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- Preparation of Nitroalkenes: Substitution Reaction via Addition-Elimination Using β-Nitrovinyl Sulfoxides
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Nitroalkenes were prepared by the substitution reaction of β-nitrovinyl sulfides and sulfoxides with a variety of carbon nucleophiles (i.e. alkylmetal reagents and enolates of carbonyl compounds), via an addition-elimination sequence.The sulfoxide as a leaving group was suitable for the reaction with an enolate of carbonyl compounds.This method was useful for the synthesis of nitroalkenes .
- Nobe, Manabu,Itoh, Akichika,Nishide, Kiyoharu,Abe, Hitoshi,Kawabata, Takeo,et al.
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p. 1119 - 1124
(2007/10/02)
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- The Photochemistry of Aliphatic and Alicyclic α,β-Unsaturated Nitro Compounds. A Study of Double Bond Cleavage Following Intramolecular Cyclization and Nitro-Nitrite Rearrangement
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The light-induced intramolecular cyclization of α,β-unsaturated nitro compounds leading to double bond cleavage, which had previously been detected in a small number of β-nitrostyrenes and α-nitrostilbenes, has been shown to occur in a range of aliphatic and alicyclic α,β-unsaturated nitro compounds.At room temperature the reaction competes to a significant extent with the well known nitro-nitrite rearrangement in the irradiation of 1-nitro-2-phenylcyclohexene (2), 1-methyl-2-nitrocyclohexene (6), 1-methyl-2-nitrocycloheptene (11), 2-methyl-3-nitrobut-2-ene (23)and 2-nitro-3-phenylbut-2-ene (24), while it was the only reaction detected in the case of 1-methyl-2-nitrocyclooctene (12) and 1-nitrocyclooctene (19).No evidence for the cleavage reaction was found with 1-methyl-2-nitrocyclopentene (10), 1-nitrocyclohexene (17), 1-nitrocycloheptene (18) and 3-nitropent-2-ene (25).The nitrile oxides produced in the double bond cleavage reaction were trapped in a cycloaddition with methyl acrylate, yielding 3-substituted methyl 4,5-dihydroisoxazole-5-carboxylates.Irradiations of 1-methyl-2-nitrocyclohexene (6) and 1-methyl-2-nitrocycloheptene (11) in refluxing benzene afforded only the bridged ring isoxazolines (30) and (31) respectively.Syntheses of a number of nitro-olefins are also reported.
- Grant, Richard D.,Pinhey, John T.
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p. 1231 - 1244
(2007/10/02)
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- Preparation of α-Nitro Olefins from α-Halo Ketoximes
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α-Nitro olefins were synthesized from α-haloketones through oximation and subsequent oxidation with trifluoroperacetic acid.
- Sakakibara, Tohru,Ikeda, Yutaka,Sudoh, Rokuro
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p. 635 - 636
(2007/10/02)
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