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1.
Renata Kolano? Teresa Borowiak Grzegorz Dutkiewicz 《Journal of Molecular Structure》2005,737(1):75-81
The X-ray and spectroscopic results clearly indicate that the (+)-2-thiono-17-oxosparteine (1) and (+)-2,17-ditihionosparteine (2) are conformationally rigid. In order to analyze deviations of lactam/thiolactam groups from planarity induced by ring constraints, the Dunitz-Winkler approach has been used. The lactam and thiolactam groups are close to planarity, only the lactam group in one of the two independent molecules of 1 is markedly non-planar. The bond angles in the thiolactam and lactam groups are highly diverse. Rings A and C adopt a distorted sofa conformation in both compounds. The distortions in the molecules of 2 as compared with those in the related monothiolactams correspond to the unusual chemical shifts of H5(eq), H5(ax) and H11, as well as to the extremely low J5ax-6 and extremely large J5eq-6 coupling constants. Also chemical shifts show a similar regularity being extremely high and low for C2 and C17, respectively. 相似文献
2.
The unrestricted Hartree-Fock (UHF) method of Snyder and Amos is used to calculate, in the -electron approximation, the spin density distributions in radical anions of heterocyclic amine N-oxides. The computed spin densities are observed to be in good agreement with the experimental values. The computed spin density distribution of the radical anion of pyridine N-oxide is consistent with the greater susceptibility of pyridine N-oxide relative to pyridine to electrophilic nitration. Also, the calculations are consistent with the lower basicity of the N-oxides relative to the parent bases. 相似文献
3.
The reaction of the dimethoxyaminyl radical with functionally substituted nitrosoalkanes (2) in a 2:1 ratio at 20°C gives the corresponding N-alkyl-N-methoxydiazene N-oxides (3) as a single isomer in preparative yields.N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences, 117913 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 10, pp. 2443–2445, October, 1992. 相似文献
4.
An O-methylated analog of protonated phenazine-di-N-oxide radical anion abstracts hydrogen from primary and secondary alcohols
in a slow (k
1 < 500 M−1 s−1) bimolecular reaction. No kinetic evidence has been found for the unimolecular release of free methoxyl radicals through
the homolytic N-OMe bond cleavage in these species. DFT calculations at the UB3LYP 6-31G(d) level indicate that protonated
and O-alkylated radical anions of pyrazine, quinoxaline and phenazine di-N-oxides are close analogues of aromatic nitroxyl
radicals with the highest spin density localized on the oxygen and nitrogen of the nitrone moiety. 相似文献
5.
A simple and precise method was developed for the analytical and preparative reversed-phase HPLC separation of a mixture of epimeric pavine N-oxides containing 49.1% of (−)-thalimonine N-oxide A and 50.1% of (−)-thalimonine N-oxide B isolated from Thalictrum simplex L. (Ranunculaceae). A reversed-phase system with Nucleosil C18 analytical and preparative columns and ethanol-1.5% aqueous orthophosphoric acid (15:85) as the mobile phase was used. The epimeric pavine N-oxides were completely separated within 50 min. 相似文献
6.
Straight-chain aliphatic terr-amine N-oxides were found to be useful oxidizing agent for epoxidation of tri- and tetra-substituted perfluoroalkenes under mild conditions in high yields.The process for epoxidation by employing tri-n-butylamine N-oxide gave the best result in the reagent survey. 相似文献
7.
W. Szczepankiewicz J. Suwinski Z. Karczmarzyk 《Chemistry of Heterocyclic Compounds》2004,40(6):801-806
The reaction of N-phenylbenzamidine with O-acetylbenzeneoximoyl chloride in methanol solution gave unexpectedly 5-methoxy-3,4,5-triphenyl-4,5-dihydro-1,2,4-oxadiazole, which structure was confirmed by X-ray analysis. The last step of this reaction was simulated by the PM3 semiempirical method. 相似文献
8.
9.
Hui Hu Xiaoping Hu Prof. Yuanhong Liu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(43):19137-19141
An efficient copper-catalyzed regioselective C−H alkenylation and borylative alkylation of quinoline N-oxides with vinyl arenes in the presence of pinacol diborane has been developed. The reaction proceeds through the borylcupration of the vinyl arenes followed by nucleophilic attack of the resulting alkyl copper species to the quinoline N-oxides. Benzoquinone and KOtBu were identified as the necessary additives at the second step of the reaction that are crucial for the success of the reaction. A wide range of C2-functionalizaed quinolines were obtained with good functional group tolerance, which may find utilities in pharmaceuticals and synthetic chemistry. 相似文献
10.
Thermal oxidative destruction of complexes of heterocyclic N-oxides with Zn(II)tetra-phenylporphyrin
N. Sh. Lebedeva W. Zielenkiewicz E. Utzig Y. A. Gubarev V. P. Andreev Ya. P. Nizhnik 《Journal of Thermal Analysis and Calorimetry》2008,91(2):601-608
Thermogravimetry, differential thermal analysis and differential scanning calorimetry were applied for investigation of molecular
complexes of heterocyclic N-oxide with zinc(II)tetraphenylporphyrin. The kinetic characteristics of the process of the thermal
oxidative destruction for individual compounds and their molecular complexes have been calculated. The obtained results indicate
that the complex formation of ZnTPhP with heteroaromatic N-oxides leads to an increase of the thermal stability both the metalloporphyrin
and the ligands. It has been shown that the stability of the molecular complexes of ZnTPhP with heteroaromatic N-oxides depends
on basicity of the coordinated ligand. 相似文献