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11.
A. S. Ermakov S. A. Serkov V. A. Tartakovskii T. S. Novikova L. I. Khmel'nitskii 《Russian Chemical Bulletin》1995,44(4):699-701
TheN-nitro derivatives of the products of the condensation of formaldehyde with sulfamic acid derivatives and guanidine, nitroguanidine, 3,4-diaminofurazan, and 3-amino-4-methylfurazan have been synthesized.Deceased.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 719–721, April, 1995. 相似文献
12.
O. A. Luk'yanov V. P. Gorelik V. A. Tartakovskii S. S. Novikov 《Russian Chemical Bulletin》1971,20(8):1696-1697
Conclusions The nitration of the sodium salts of sulfamides with nitrogen pentoxide leads to the formation of the corresponding N-nitrosulfamides.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1804–1806, August, 1971. 相似文献
13.
Conclusions The silylation of 5-chloromethyl-2-isoxazoline-3-carboxylic acid with the usual silylating agents leads to the corresponding trimethylsilyl ester, which when heated is converted to 4-chloro-3-trimethylsiloxybutyronitrile.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2818–2819, December, 1981. 相似文献
14.
I. E. Chlenov I. M. Petrova V. M. Shitkin V. A. Tartakovskii 《Russian Chemical Bulletin》1976,25(6):1347-1350
1. | The reaction of 6-nitro-2,9-dioxa-1-azabicyclo[4.3.0]nonane derivatives with alcohols and alcoholates leads to remplacement of the nitro group by the corresponding alkoxy group. |
2. | The reaction proceeds with either a complete (for the case of the alcoholates) or predominant (for the case of alcohols) inversion of the configuration at the substitution center. |
3. | The reaction proceeds via the intermediately formed bicyclic immonium cation. |
15.
Laurence E. Strong Carter Van Waes Kenneth H. Doolittle II 《Journal of solution chemistry》1982,11(4):237-258
The three monofluorobenzoic acids together with 2,4-difluoro and 2,6-difluorobenzoic acids in aqueous solution are the subject of precision conductance measurements. The experimental data are analyzed to give ionization constants and limiting conductances at temperatures from 0 to 100°C. Walden products for the acid anions are derived from the limiting conductances while the ionization consatants are fitted by statistical methods to the function pK
a
(m)=A+B/T+ C logT+DT. Only the 2,6- acid requires the fourth term of the function to fit the data to a precision of better than 0.03%. Mathematical analysis of the pK function gives the standard changes in enthalpy, entropy, and heat capacity. All the acids studied are more acidic than the parent, benzoic acid, as well as more acidic than the isoelectronic methylbenzoic acids. In general the increased acidity is tied to decreases in enthalpy while entropy changes on ionization differn little from those found for the parent acid. 相似文献
16.
Tartakovskii V. A. Shevelev S. A. Dutov M. D. Serushkina O. V. Kachala V. V. 《Russian Journal of Organic Chemistry》2003,39(3):397-402
Treatment of 2,4,6-trinitrotoluene with -mercaptocarboxylic acid esters and subsequent oxidation gave 2-(alkoxycarbonyl-R-methylsulfonyl)-4-X-6-nitrotoluenes which were brought into Knoevenagel condensation with aromatic aldehydes (heating in benzene in the presence of secondary amine acetates). As a result of intramolecular cyclization, 2-alkoxycarbonyl-3-aryl-2-R-5-X-7-nitrothiochroman 1,1-dioxides (R = H, Me; X = NO2, R'SO2) were obtained. The developed procedure opens the way to hitherto unknown thiochroman 1,1-dioxide derivatives. 相似文献
17.
18.
Mahesh Attimarad Katharigatta Narayanaswamy Venugopala Muhammad S. Chohan Marysheela David Efren II Plaza Molina Nagaraja Sreeharsha Anroop Balachandran Nair Christophe Tratrat Abdulrahman Ibrahim Altaysan Abdulmalek Ahmed Balgoname 《Molecules (Basel, Switzerland)》2022,27(10)
A rapid and reproducible hydrophilic liquid chromatography (HILIC) process was established for concomitant determination of remogliflozin etabonate (RE), vildagliptin (VD), and metformin (MF) in a formulation. A face-centered central composite experimental design was employed to optimize and predict the chromatographic condition by statistically studying the surface response model and design space with desirability close to one. A HILIC column with a simple mobile phase of acetonitrile (65% v/v) and 20 mM phosphate buffer (35% v/v, pH 6, controlled with orthophosphoric acid) was used to separate RE, VD, and MF. RE, VD, and MF were separated in 3.6 min using an isocratic mode mobile phase flow at a flow rate of 1.4 mL at room temperature, and the analytes were examined by recording the absorption at 210 nm. The developed HILIC method was thoroughly validated for all parameters recommended by ICH, and linearity was observed in the ranges 20–150 µg/mL, 10–75 µg/mL, and 50–750 µg/mL for RE, VD, and MF, respectively, along with excellent regression coefficients (r2 > 0.999). The calculated percentage relative deviation and relative error ascertained the precision and accuracy of the method. The selectivity and accuracy were further confirmed by the high percentage recovery of added standard drugs to the formulation using the standard addition technique. The robustness of the HILIC processes was confirmed by developing a half-normal probability plot and Pareto chart, as the slight variation of a single factor had no significant influence on the assay outcomes. Utilization of the optimized HILIC procedure for concurrent quantification of RE, VD, and MF in solid dosage forms showed accurate and reproducible results. Hence, the fast HILIC method can be regularly employed for the quality assurance of pharmaceutical preparations comprising RE, VD, and MF. 相似文献
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