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排序方式: 共有238条查询结果,搜索用时 15 毫秒
1.
Davydov V. V. Al-Salekh O. A. Mercur'eva N. Yu. Ryabov M. A. Sokol V. I. Sergienko V. S. Shklyaev Yu. V. 《Russian Journal of Coordination Chemistry》2003,29(1):16-21
Twenty new complexes were synthesized by reacting Co(II), Cu(II), Zn, Cr(III), Fe(III), Cd and Ag salts with 3,3-dimethyl-1-(3-methylpyrazole-5-onilidene-4)-1,2,3,4-tetrahydroisoquinoline (L1), spiro{cyclohexane-1,3"-[1-(1-phenyl-3-methylpyrazole-5-onilidene-4)-1,2,3,4-tetrahydroisoquinoline]} (L2), and 3,3-dimethyl-1-(1-phenyl-3-methylpyrazole-5-onilidene-4)-1,2,3,4-tetrahydroisoquinoline (L3). These compounds were studied by IR and electronic absorption spectroscopy. The type of coordination of their ligands was discussed on the basis of the results obtained and X-ray diffraction data for L3 and [CuL2
2 Cl2] · 2L2 obtained previously. 相似文献
2.
A. G. Mikhailovskii V. S. Shklyaev G. A. Veikhman M. I. Vakhrin 《Chemistry of Heterocyclic Compounds》1993,29(10):1178-1181
We have synthesized secondary and tertiary enamines, derivatives of 1,2,3,4,4a,5,6,10b-octahydrophenanthridine, and we have considered the Z,E-isomerism of the enaminoesters.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1374–1377, October, 1993. 相似文献
3.
3,3-Dimethyl-1-hydrazono-1,2,3,4-tetrahydroisoquinoline derivatives react with benzil in 1 : 1 or 2 : 1 ratio to give the corresponding benzil monohydrazones. Diacetyl under the same conditions forms dihydrazones. Enolizing 1,3-dicarbonyl compounds form with 3,3-dimethyl-1-hydrazono-1,2,3,4-tetrahydroisoquinoline derivatives mixtures of mono- and dihydrazones. Dehydracetic acid forms monohydrazones at the exochain carbonyl group. 相似文献
4.
A. G. Mikhaflovskii V. S. Shklyaev A. V. Ignatenko M. I. Vakhrin 《Chemistry of Heterocyclic Compounds》1995,31(7):813-816
Reactions between 2,3-dioxopyrrolo[2,1-a]-isoquinolines and hydrazines and hydroxylamine afforded the corresponding hydrazones and oximes.Institute of Applied Chemistry, Urals Branch, Russian Academy of Sciences Perm' 614600. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 934–937, July, 1995. Original article submitted May 5, 1995. 相似文献
5.
B. B. Aleksandrov M. Yu. Dormidontov V. S. Shklyaev Yu. V. Shklyaev 《Chemistry of Heterocyclic Compounds》1991,27(5):523-525
The Ritter reaction between -substituted propionitriles and dimethylbenzylcarbinols gives 3,3-dimethyl-3,4-dihydroisoquinolines containing substituents in the 1-position corresponding to those in the starting nitrile.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 657–659, May, 1991. 相似文献
6.
V. Yu. Tyutin N. D. Chkanikov V. S. Shklyaev Yu. V. Shklyaev A. F. Kolomiets A. V. Fokin 《Russian Chemical Bulletin》1992,41(8):1474-1476
1,3,3-Trimethyl-3,4-dihydroisoquinolines react with 1,1-dicyano-2,2-bis(trifluoromethyl)ethylene to give 4-amino-6,6-dimethyl-2,2-bis(trifluoromethyl)-3-cyano-6,7-dihydro-2H-benzo[a]quinolizines. The reaction of 3,3-dimethyl-1-cyanomethylidene-1,2,3,4-tetrahydroisoquinoline and the methyl ester of 3,3-dicyano-2-(trifluoromethyl)acrylic acid leads to 5,5-dimethyl-3-oxo-2-(trifluoromethyl)-2-(dicyanomethyl)-2,3,5,6-tetrahydropyrrolo[2,1-a]isoquinoline.A. N. Nesmeyanov Institute of Heteroorganic Compounds, Russian Academy of Sciences, 117813 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 8, pp. 1888–1892, August, 1992. 相似文献
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9.
V. I. Sokol O. A. Yakimenko V. V. Davydov Yu. V. Shklyaev V. S. Sergienko M. A. Ryabov 《Chemistry of Heterocyclic Compounds》2002,38(12):1497-1503
3,3-Dimethyl-1-(3-methyl-1-phenylpyrazol-5-onylidene-4)-1,2,3,4-tetrahydroisoquinoline has been synthesized and its crystalline and molecular structures determined. It was found by IR and electronic absorption spectroscopic methods that the structure of this compound is not changed in solutions. 相似文献
10.