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1.
The transannular cycloaddition between the double bond on the side chain and the -benzoquinone ring in -C8-bridged -benzo-quinones by way of an oxyallyl intermediate is described. 相似文献
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The nitration of -cresol by nitric acid in aqueous sulphuric acid involves ~40% -substitution at CMe. The 4-methyl-4-nitrocyclohexa-2,5-dien-1-one (I) formed undergoes an acid-catalysed rearrangement to 4-methyl-2-nitrophenol. 相似文献
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The cycloaddition of the dispiro compound, , with a variety of 1,3-butadienes affords diacetates of -C8-bridged hydroquinones, which are led to the corresponding hydroquinones and -benzoquinones. 相似文献
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Diastereoisomers of 1,4-dimethyl-4-nitro-2,5-cyclohexadienyl acetate exchanged acetoxyls for alkoxyls on irradiation in alcohols to give the diastereoisomers of alkyl, 1,4-dimethyl-4-nitro-2,5-cyclohexadienyl ethers in isomer ratios of 70:30, whereas the irradiation in pentane yielded -xylene. 相似文献
5.
Nmr and UV studies show that -dimethylamino--bromostyrene, I, undergoes SNl reaction in H2O and HClO4 (kSNl = 6 × 10?1sec.?1 at 25°). The vinyl cation has an extraordinary selectivity for capture by aromatic amines relative to H2O, including I itself to give the dimer II. 相似文献
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The Diels-Alder reaction of -benzoquinone with substituted dienoic esters affords good yields of 4a,5,8,a-tetrahydro-1,4-naphthalenediones, free from the isomeric hydroquinone. The reactions were conducted at room temperature under 15 kbar (1.5 GPa) pressure in dichloromethane solutions. 相似文献
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Monomeric -dimethylamino--bromostyrene undergoes SNl increasingly slowly in 60 to 91% dioxane. Reaction is catalyzed by HClO4, NaOH and NaClO4. Dimer 11 reverts to monomer I in 91% dioxane. There is only a small solvent effect on the solvolysis rate of II. 相似文献
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Superoxo Co(III) complexes derived from Co(Salpr) and [Co(CN)5]3? reacted with 2,6-di--butyl--benzoquinone methides to give 2,6-di--butyl--benzoquinone and 2,6-di--butyl-2,5-cyclohexadienonespirooxiranes as the main products, which are considered to result from nucleophilic attack by the superoxo species on the exo double bond of the quinone methides. 相似文献
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Rudolph A. Abramovitch Suchet S. Mathur Daniel W. Saunders Danny P. Vanderpool 《Tetrahedron letters》1980,21(8):705-708
Pyridinium -toluenesulfonylmethylide serves as a formyl anion equivalent and, in the presence of an alcohol, undergoes 1,4-addition to -substituted maleimides to give alkoxy- (or aryloxy)-methylene-succinimides. The protected aldehyde group can be liberated readily. 相似文献
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J Leitich 《Tetrahedron letters》1980,21(32):3025-3028
The relative rates of formation of and [2+2]cycloadducts of benzyne to , - and , -1,5-cyclooctadiene, - and -cyclooctene are discussed and properties of the adducts (e.g., their unusual hydrogenation) are described. 相似文献
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All four isomers of substituted 3-alkylthio-4-hydroxybutenes have been synthesised: both the geometry of the double bond and the relative stereochemistry of the two chiral centres are controlled. 相似文献
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Photolysis of -butyl azide in N2 matrices at 12 K gives the imine 3a; matrix IR spectra for imines 4a and 5a are also reported. 相似文献