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1.
The reactions of 2,3,6,11-tetrahydroanthra[2,1-d]isothiazole-3,6,11-trione with dimethyl sulfate, benzyl chloride, and allyl bromide afforded the corresponding 2-alkyl-2,3,6,11-tetrahydroanthra[2,1-d]isothiazole-3,6,11-triones and 3-(alkoxy)-6,11-dihydroanthra[2,1-d]isothiazole-6,11-diones. The reactions of 2,3,6,11-tetrahydroanthra[2,1-d]isothiazole-3,6,11-trione and its S-oxide with a formaldehyde—secondary amine system yielded 2-[(alkylamino)methyl]-2,3,6,11-tetrahydroanthra[2,1-d]isothiazole-3,6,11-triones and 2-[(alkylamino)methyl]-3,6,11-trioxo-2,3,6,11-tetrahydroanthra[2,1-d]isothiazole 1-oxides, respectively. 相似文献
2.
Zh. A. Krasnaya E. O. Tret’yakova V. V. Kachala S. G. Zlotin 《Russian Chemical Bulletin》2008,57(8):1671-1675
A reaction of 2,2-disubstituted 1,1-dicyanoethenes with β-dimethylaminoacrolein aminal and 3-dimethylamino-1,1,3-trimethoxypropane
leads to substituted 6,6-dicyano-1-dimethyl-aminohexatrienes and an organic salt containing 1,1,9,9-tetracyano-2,8-diphenylnona-2,4,6,8-tetraenide
as the anion and (dimethylaminopropenylidene)dimethylammonium as the cation, on the basis of which new cation-anionic polymethine
dyes were obtained.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1639–1643, August, 2008. 相似文献
3.
Nitro derivatives of 1-R-1,2-benzoisothiazol-3-one 1-oxide were synthesized by the reactions of 2-alkyl(phenyl)thio-4-nitro- and 4,6-dinitro-2-(phenylthio)benzamides with chlorine in 60% acetic acid. Analogous reactions of 2-(n-butylthio)-4-nitro- and 2-(tert-butylthio)-4-nitrobenzamides with chlorine afforded 2-butyl- and 2-H-1,2-benzoisothiazol-3-one 1-oxides, respectively. The proposed reaction mechanism includes the formation and subsequent transformations of S-alkyl-S-aryl- and S,S-diarylchlorosulfonium chlorides. 相似文献
4.
S. G. Zlotin O. V. Prokshits N. F. Karpenko Yu. A. Strelenko O. A. Luk'yanov 《Russian Chemical Bulletin》1992,41(8):1400-1413
We have worked out a method for the synthesis of 1,3,3-trisubstituted triazene 1-oxides based upon reaction of 1,1-disubstituted hydrazines with bromine in the presence of aryl- and heteroarylnitroso compounds in acid media. Obtained are a broad range of triazene 1-oxides, among which hitherto unknown compounds of the series of pyrazole and 3,3-dialkyltriazene 1-oxides that contain functional groups at the alkyl part of the molecule. We propose a reaction scheme which includes in situ formation of diazenium cations and reaction of them with nitroso compounds that are present in the system. By means of PMR,13C, and14N NMR spectroscopy, and mass spectroscopy, it has been shown that in all the prepared compounds the oxidated nitrogen atom is at the N1 position of the triazene N-oxide group.N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 8, pp. 1804–1820, August, 1992. 相似文献
5.
A one-step synthesis of alkylN-(-amidomethyl)glycinates from glycine esters or their salts, formaldehyde, and aroylamides was developed. The effect of the structure of the amide component and the reaction conditions on the yields of the products was investigated.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1078–1080, June, 1994. 相似文献
6.
S. G. Zlotin M. V. Sharashkina Yu. A. Strelenko O. A. Luk'yanov M. O. Dekaprilevich Yu. T. Struchkav 《Russian Chemical Bulletin》1994,43(7):1220-1226
Methods for the synthesis of polyfunctionalN-phosphoryl- andN-phosphonoyldiazeneN-oxides containing hydroxyl, acetoxyl, and nitrate groups, and dibromoallyl and dibromopropyl fragments have been developed. The molecular structure ofN-(2,2-dimethyl-5-nitro-1,3-dioxan-5-yl)-N-[methoxy(phenyl)phosphoryl)diazeneN-oxide was established by X-ray structural analysis.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1284–1289, July, 1994. 相似文献
7.
When treated with an excess of MeONa in DMF, 5-benzylsulfonyl-3-chloro-4-methoxycarbonylaminoisothiazole undergoes cyclization into 3-methoxy-5-oxo-6-phenyl-5,6-dihydro-4H-isothiazolo[5,4-b]-1,4-thiazine 7,7-dioxide, the first representative of a new heterocyclic system. The starting 5-benzylsulfonyl-3-chloro-4-methoxycarbonylaminoisothiazole was prepared by the reaction of 5-benzylsulfonyl-4-carbamoyl-3-chloroisothiazole with PhI(OAc)2 in methanol. 相似文献
8.
N-Nitroso,N-sulfonyl, andN-acyl derivatives ofN-(amidomethyl)- andN-(imidomethyl)-glycine esters have been synthesized by the reactions of these esters with HNO2 or with sulfonylating and acylating reagents.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1299–1305, July, 1995. 相似文献
9.
Dmitry E. Siyutkin Alexander S. Kucherenko Larisa L. Frolova Alexander V. Kuchin Sergei G. Zlotin 《Tetrahedron: Asymmetry》2013,24(12):776-779
Novel stereoisomeric natural pinane-derived bifunctional catalysts 3a–d bearing a pyrrolidine unit have been synthesized and examined in the asymmetric conjugate additions of carbonyl compounds to α-nitroalkenes. Six-membered cyclic ketones react with β-nitrostyrene derivatives in the presence of (1R,2R,3R,5R)-2-hydroxy-3-((S)-pyrrolidin-2-ylmethylamino) pinane 3b (10 mol %) with high conversion to afford with diastereoselectivity (dr (syn/anti) up to 97/3), the corresponding Michael adducts with enantiomeric purities of up to 88% ee. 相似文献
10.
Nina I. Simirskaya Nikolai V. Ignat’ev Michael Schulte Sergei G. Zlotin 《Mendeleev Communications》2012,22(6):317-319
Terminal alkynols react with formaldehyde and secondary amines in aqueous ionic liquid [emim]HSO–4 in the presence of Cu(OAc) to afford the corresponding 1-(a-hydroxyalkyl)- or 1-(b-hydroxyalkyl)-2-(aminomethyl)acetylenes in better yields in comparison with the reaction in conventional organic solvents. The catalytic system can be easily recovered and recycled. 相似文献