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1.
Data on methods for the production of isatin and indole aldoximes, ketoximes, and amidoximes and their reactions are reviewed. Individual syntheses of new heterocycles from indole and isatin oximes are discussed. The principal results from investigation of the biological activity of derivatives of the oximes are also presented. 相似文献
2.
Reactions of acetone, cyclohexanone, and adamantanone oximes withN,N-dibromo-tert-butylamine result in the correspondingC-bromo-diazene-N-oxides. In the case of benzophenone oxime,O, O'-(diphenylmethylene)-bis-benzophenone oxime has been obtained.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 176–177, January, 1994. 相似文献
3.
Sulfonyldiazene-N-oxides2 and3 were obtained by treatment of sulfamide with nitroso compounds1 in the presence of 1,3-dibromoisocyanurate (DBI) in neutral and acid media.Translated fromIzyestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 681–683, April, 1994. 相似文献
4.
W. Fleischhacker K. Florkova B. Richter 《Monatshefte für Chemie / Chemical Monthly》1994,125(3):345-353
Summary Following our concept of rather new structural variations in the nitrogen region of morphine alkaloids we describe the first synthesis of N/C-10-bridged tertiary bases. 相似文献
5.
D iels-A lder反应具有立体专一性和很好的区域选择性,已被大量应用于天然有机化合物、香料、药物等的合成中。一般说来,D iels-A lder反应在加热条件下即能发生,但加热往往导致反应的区域选择性和立体专一性下降,而研究表明,路易斯酸催化下的D iels-A lder反应在不同程度上表现出或反应速度加快,或产率提高,或条件温和,尤其是区域选择性和立体专一性得到提高等良好特性。呋喃类化合物由于呋喃环所具有的芳香性而较难与一般的亲双烯发生D iels-A lder反应。如呋喃和丙烯酸甲酯在加热条件下反应2~3个月,产率只能达到50%,且反应温度的提高… 相似文献
6.
Yarovenko V. N. Kosarev S. A. Zavarzin I. V. Krayushkin M. M. 《Russian Chemical Bulletin》2002,51(8):1504-1509
Carbamoylformhydroxymoyl chlorides were synthesized by the reactions of carbamoylformamide oximes with sodium nitrite in the presence of hydrochloric acid, and their reactivities were examined. 相似文献
7.
N. S. Arutyunyan L. A. Akopyan G. A. Gevorgyan G. M. Snkhchyan G. A. Panosyan 《Chemistry of Heterocyclic Compounds》2005,41(4):437-441
A preparative method was developed for the synthesis of ethyl furfurylidenecyanoacetate. Its condensation with phenylmagnesium bromide gave ethyl α-cyano-β-(2-furyl)hydrocinnamate, the decarboxylation of which led to β-(2-furyl)hydrocinnamonitrile. Reduction of this nitrile with lithium aluminum hydride gave 2-(3-amino-1-phenylpropyl)furan. Some of its transformations were studied.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 517–521, April, 2005. 相似文献
8.
An efficient synthesis of 6-azapregnane derivatives and their biological activity is described. The nitrogen was introduced into the B ring using Beckmann rearrangement of the (E)-oxime of 6-oxo-B-nor-5α-pregnane derivatives. The required 3α-hydroxyl was produced either by solvolysis of the corresponding 3β-mesyloxy group or by the Meerwein-Ponndorf-Verley reduction of the 3-oxo group; this reduction could be carried out selectively with an unprotected 3,20-dioxo derivative. The binding of the 6-aza-steroids to the γ-aminobutyric acid receptor (GABAA) was measured using [35S]-tert-butyl-bicyclo[2.2.2]phosphorothionate (TBPS) and [3H]flunitrazepam. The only analogue to be slightly active was that lacking any oxygen function in position 3. 相似文献
9.
Vyacheslav Ya. Sosnovskikh Boris I. Usachev Mikhail I. Kodess 《Tetrahedron letters》2004,45(39):7351-7354
Reactions of chromones with dilithiooximes proceed via nucleophilic 1,2-addition to give, on acidification, 4H-chromene-4-spiro-5′-isoxazoline derivatives in high yields. On treatment with concentrated H2SO4 the isoxazoline ring of this novel spiroannulated heterocyclic system opens to give α,β-unsaturated oximes, which undergo nitrosation, bromination, and the Beckmann rearrangement to the corresponding spiroisoxazolines and α,β-unsaturated amides, respectively. The latter can be obtained directly by the Beckmann rearrangement of 4H-chromene-4-spiro-5′-isoxazolines. 相似文献
10.
E. A. Dikusar N. G. Kozlov V. I. Potkin T. D. Zvereva A. P. Yuvchenko M. P. Bei N. V. Kovganko 《Chemistry of Natural Compounds》2006,42(5):539-542
Previously unreported esters 1b–20b were synthesized from natural terpene alcohols, sterols, plant phenols, and camphar oxime (1a–20a) by reaction with o-carborane-C-carboxylic acid chloride.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 434–436, September–October, 2006. 相似文献