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《Tetrahedron: Asymmetry》2006,17(1):79-91
Reductions of (1R,3R,4R)-3-([1,2,4]triazolo[4,3-x]azin-3-yl)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ones and their lactone analogues, prepared from (1R)-(+)-camphor, were studied. Catalytic hydrogenation selectively led to partial saturation of the [1,2,4]triazolo[4,3-x]azine residue, while in reactions with borane–methylsulfide coordination of borane to the 1-position of [1,2,4]triazolo[4,3-x]azine system took place. On the other hand, activation of the carbonyl group in (1R,3R,4R)-3-([1,2,4]triazolo[4,3-x]azin-3-yl)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ones with boron trifluoride etherate followed by reaction with borane–methylsulfide furnished the corresponding isoborneols, stereoselectively. The structures of all representative compounds were confirmed by X-ray diffraction. 相似文献
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Pitushkin D. A. Burmistrov V. V. Saeef M. H. Abbas Vernigora A. A. Butov G. M. 《Russian Journal of Organic Chemistry》2020,56(11):1893-1904
Russian Journal of Organic Chemistry - A series of 1,3-disubstituted ureas containing a bicyclic lipophilic group of natural origin were synthesized by the reactions of bicyclo[2.2.1]heptane-2-yl... 相似文献
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A. V. Bogdanov V. F. Mironov N. R. Khasiyatullina D. B. Krivolapov I. A. Litvinov A. V. Kuchin A. I. Konovalova 《Russian Chemical Bulletin》2006,55(2):396-398
The reaction of 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione with hexaethyltriamido-phosphite in the presence of diethylammonium
chloride afforded a stable quasiphosphonium salt, viz., (1,7,7-trimethyl-2-oxobicyclo[2.2.1]hept-3-yloxy)tris(diethylamino)phosphonium chloride, as one diastereomer (racemate,
1R*,3S*,4S*).
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 383–385, February, 2006. 相似文献
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The photolysis of 3-ethoxyimino-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 1 with λ 254 nm has been investigated in acetonitrile as solvent. Photoexcited 1 undergoes N-O bond homolysis with formation of a cyclic α-oxo-iminyl and an ethoxy radical. Cage recombination of these radicals affords the ethyl cyanocyclopentanecarboxylate 9. The formation of the products 6–8 is explained by decarbonylation of the α-oxo-iminyl radical, followed by disproportionation and H-abstraction. The occurrence of the α-oxo-iminyl radical and (by loss of CO) the tertiary cyanocyclopentyl radical is substantiated by an ESR photoexperiment in the presence of 2-methyl-2-nitrosopropane. 相似文献
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3-exo-Hydroxymethyl-5,5,6-trimethylbicyclo[2.2.1]heptan-2-one was prepared by treatment of isocamphanone with Paraform in the presence of alkali in DMF. The product reacts with acetonitrile in the presence of sulfuric acid (Ritter reaction) to form a mixture of 2-(acetylamino)-3-(acetylaminomethyl)-5,5,6-trimethylbicyclo[2.2.1]hept-2-ene and 2,2-bis(acetylamino)-3-(acetylaminomethyl)-5,5,6-trimethylbicyclo[2.2.1]heptane in a 1:1 ratio. Attempted hydroxymethylation of isocamphanone in DMSO gave bis(isocamphanon-3-endo-yl)methane. 相似文献
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M. G. Veliev M. M. Guseinov L. A. Yanovskaya R. F. Gakhramanov 《Russian Chemical Bulletin》1982,31(11):2282-2285
Conclusions The Grignard reagent, obtained from 5-(propyn-2-yl)bicyclo[2.2.1]-2-heptene, reacts easily with Ac2O, Et2SiCl2, Me3SiCl, and acrolein to give in high yields [2.2.1]bicyclo-2-heptene derivativesthat contain in the side chain either an acetyl, diethylsilyl, trimethylsilyl, or a hydroxypropen-1-yl group. The Mannich reaction was also run with 5-(propyn-2-yl)bicyclo[2.2.1]-2-heptene.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2586–2589, November, 1982. 相似文献
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Mamedov M. K. Piraliev A. G. Rasulova R. A. 《Russian Journal of Applied Chemistry》2009,82(3):515-517
Russian Journal of Applied Chemistry - Bicyclic esters, which are reactive monomers for the synthesis of new polymeric products and also of organic compounds, were synthesized by the reaction of... 相似文献
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Nosova E. V. Kopotilova A. E. Ivan’kina M. A. Moshkina T. N. Kopchuk D. S. 《Russian Chemical Bulletin》2022,71(7):1483-1487
Russian Chemical Bulletin - A series of [1,2,4]triazolo[4,3-c]quinazolines, bearing 3-positioned p-bromophenyl or 5-bromothiophen-2-yl fragment, was synthesized by oxidative cyclization of the... 相似文献
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V. A. Pal’chikov S. A. Prid’ma L. I. Kas’yan 《Russian Journal of Organic Chemistry》2014,50(9):1312-1316
A new N-(oxiran-2-ylmethyl) (glycidyl) derivative has been obtained by reaction of N-(bicyclo-[2.2.1]hept-5-en-endo-2-ylmethyl)(7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonamide with epichlorohydrin. Its epoxidation and aminolysis have been studied, and the regioselectivity of these transformations has been determined by IR and 1H NMR spectroscopy and mass spectrometry. 相似文献
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A number of derivatives of 5-(2-aminoethyl)bicyclo[2.2.1]hept-2-ene (85-90% of the endo isomer) were synthesized by reactions with p-nitrobenzenesulfonyl chloride, p-toluenesulfonyl chloride, benzoyl chloride, p-nitrobenzoyl chloride, benzyl isocyanate, m-tolyl isocyanate, phenyl isothiocyanate, and endic anhydride. By reactions of the resulting sulfon- and carboxamides with peroxyphthalic acid generated in situ from phthalic anhydride and 40-45% hydrogen peroxide the corresponding epoxy derivatives were obtained. These reactions were not accompanied by heterocyclization into azabrendane derivatives, which is typical of homologous N-(p-nitrophenylsulfonyl)-endo-5-aminomethylbicyclo[2.2.1]hept-2-ene. 相似文献