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1.
A. V. Anisimov A. A. Grishkyan Kh. A. Gaisina E. A. Viktorova 《Chemistry of Heterocyclic Compounds》1994,30(4):420-421
1-Allyloxy-2-allylthio-4-methylbenzene rearranges in NN-diethylaniline at 215°C with migration of allyloxy and allylthio groups to form 2,4-dimethyl-6-allyl-7-hydroxy-2,3dihydrobenzothiophene.M. V. Lomonosov State University, Moscow 119899. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 480–482, 1994. Original article submitted March 5, 1994. 相似文献
2.
T. A. Danilova R. G. Aukharieva S. N. Petrov S. Ya. Grobovenko E. A. Viktorova 《Chemistry of Heterocyclic Compounds》1981,17(9):883-886
The thio-Claisen rearrangement of isomeric 3- and 1-methylallyl phenyl sulfides was investigated. It is demonstrated that the thio-Claisen rearrangement of the 3-methyl isomer is preceded by its thioallyl rearrangement to the 1-methyl isomer. The latter undergoes thio-Claisen rearrangement to o-(3-methylallyl)thiophenol, which is cyclized to 2-ethyl-2,3-dihydrobenzothiophene and 2-methylthiochroman under the reaction conditions.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1191–1194, September, 1981. 相似文献
3.
É. A. Karakhanov S. Kh. Sharipova M. I. Rozhkova E. A. Viktorova 《Chemistry of Heterocyclic Compounds》1978,14(1):15-16
It is shown that the principal pathway in the reaction of benzofuran with a solution of lithium in hexametapol is opening of the furan ring of benzofuran to give a dilithium derivative. Mono- and dialkylation products are formed when the reaction mixture is treated with alkylating agents. It was established by the use of alkylating agents with different degrees of hardness that the oxygen atom is a softer polarizable center than the sp-hybridized carbanion center.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 22–23, January, 1978. 相似文献
4.
It is shown that the rearrangement of allyl 2-thienyl and allyl 3-thienyl sulfides in various solvents at 89–136°C gives the corresponding allylthiophenethiols, which can subsequently undergo transallylation with the starting sulfide and cyclization to thienodihydrothiopyrans and methyldihydrothienothiophenes. The energy of activation of the rearrangement of both isomeric sulfides is 19 kcal/mole. The pKa values of thiophenyl and some thiols of the thiophene series were determined, and it was established that the acidities of the allylthiophenethiols do not have a decisive effect on their ability to undergo cyclization.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 186–189, February, 1978. 相似文献
5.
A. K. Yus'kovich T. A. Danilova E. A. Viktorova 《Chemistry of Heterocyclic Compounds》1982,18(2):141-144
The transformations of 2-methylthiacyclobutane at 150–350 °C in the presence of -Al2O3 samples with different aprotic acidities were investigated. It was established that the sulfide undergoes isomerization via two pathways, viz., with ring expansion to a five-membered ring and with opening at one C—S bond to give an unsaturated thiol. An experimental confirmation of the consecutive formation of hydrogen sulfide from a one-ring sulfide through a step involving the formation of an unsaturated thiol was obtained for the first time. The transformations are realized as a result of both ionic and polymerization-depolymerization processes.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 184–187, February, 1982. 相似文献
6.
A. V. Anisimov G. N. Murina L. V. Mozhaeva N. B. Kazennova E. A. Viktorova 《Chemistry of Heterocyclic Compounds》1984,20(6):599-601
The direction of the reaction of alkyl furfuryl ethers and sulfides with n-butyllithium is in agreement with the results of basic H-D exchange in the same compounds: In the case of the ethers H-D exchange and metallation take place primarily in the free a position of the furan ring, whereas in the case of the sulfides these reactions take place primarily at the methylene group of the side chain located between the sulfur atom and the furan ring.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 744–746, June, 1984. 相似文献
7.
8.
P. M. Kochergin A. M. Tsyganova L. M. Viktorova 《Chemistry of Heterocyclic Compounds》1967,3(1):66-67
A number of derivatives of imidazo [5, 1-b] thiazole, imidazo [5, 1-b] thiazoline, and imidazo [5, 1-b] thiazolid-3-one are synthesized by cyclizing 2-alkyl-4(5)-nitro-5(4)-formylmethyl (-ketoalkyl-,-hydroxyethyl-, and carboxymethyl) mercaptoimidazoles.For Part XXVI see [18]. 相似文献
9.
10.
R. K. Rastsvetaeva N. V. Chukanov V. A. Zaitsev S. M. Aksenov K. A. Viktorova 《Crystallography Reports》2018,63(3):349-357
An eudialyte group mineral, found in pegmatites of the Odikhincha massif (the northern part of the Siberian platform), has been investigated using X-ray diffraction, IR spectroscopy, and Raman spectroscopy. The mineral is characterized by a high strontium content and a low chlorine content. It has a trigonal unit cell with the following parameters: a = 14.2700(6) Å and c = 30.057(1) Å; V = 5300.6(1) Å3; sp. gr. R3m. The structure has been refined to R = 0.047 in the anisotropic approximation of atomic displacements using 1697F > 4σ(F). The idealized formula (Z = 3) was found to be Na12Sr2Ca6Fe 3 2+ Zr3NbSi25O72(OH,O)4Cl(Н2О)0.2. The chemical composition and structure of this mineral are close to those of taseqite; however, it differs from the holotype sample by a low chlorine content and peculiarities of cation distribution over basic structure sites. A comparative analysis of strontium-rich eudialytes has revealed their important crystallochemical feature: selective concentration of strontium in the N4 site. Thus, taseqite, along with heterophyllosilicates, may play a role of strontium concentrator in agpaitic pegmatites. 相似文献