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1.
Raskulova T. V. Volkova L. I. Danilevich Yu. S. Shainyan B. A. Khaliullin A. K. 《Russian Journal of Organic Chemistry》2002,38(5):754-755
Russian Journal of Organic Chemistry - 相似文献
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E. N. Suslova A. I. Albanov B. A. Shainyan 《Russian Journal of General Chemistry》2005,75(8):1234-1242
Synthetic approaches to 4,4-dimethyl-1,4-thiasilinane and its S-functional derivatives, 4,4-dimethyl-1,4-thiasilinane S-oxide, 4,4-dimethyl-1,4-thiasilinane S,S-dioxide, 4,4-dimethyl- 1-(phenylsulfonylimino)-1,4-thiasilinane, and 1,4,4-trimethyl-1,4-thiasilinan-1-ylium iodide, were studied. The S-functional derivatives of 4,4-dimethyl-4-thiasilinane, unlike 3,3-dimethyl-3-thiasilinane, are hydrolytically stable. 相似文献
4.
The catalytic reduction of acetophenone, methyl α-acetamidocinnamate, and dimethyl itaconate with alcohol-modified sodium borohydride was studied in the presence of complexes CoCl2·L2 (L2 are chiral C
2-symmetric diamines: (4S,5S)-2,2-dimethyl-4,5-bis(aminomethyl)-1,3-dioxolane, (4S, 5S)-2,2-dimethyl-4,5-bis(methylaminomethyl)-1,3-dioxolane, (4S, 5S)-2,2-dimethyl-4,5-bis(dimethylaminomethyl)-1,3-dioxolane, and (4S, 5S)-2,2-dimethyl-4,5-bis(diphenylaminomethyl)-1,3-dioxolane). The maximum enantiomeric excess of (S)-1-phenylethanol was 24%, that of dimethyl α-methylsuccinate was 38%.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 342–347, February, 2005. 相似文献
5.
Nindakova L. O. Shainyan B. A. Albanov A. I. Shmidt F. K. 《Russian Journal of Organic Chemistry》2003,39(7):926-932
The catalytic activity and stereoselectivity in the hydrogenation of itaconic and -(acetylamino)cinnamic acids were studied in the presence of the complex [Rh(COD)(L1)2]+ TfO- (where COD is cyclooctadiene and L1 is (1S,2S,5R)-(+)-neomenthyldiphenylphosphine] which was generated in situ. The optical yield of the hydrogenation of itaconic acid increases both on addition of chiral (4S,5S)-(+)-2,2-dimethyl-4,5-bis(dimethylaminomethyl)-1,3-dioxolane (L2) as an auxiliary ligand to the complex [Rh(COD)(L1)2]+ TfO- and on addition of achiral and chiral tertiary phosphines to the complex [Rh(L2)2]+ TfO-. The result of joint action of two ligands can be regarded as "matched effect." Transformations of the complexes in a hydrogen atmosphere were examined by 1H and 3
1P NMR spectroscopy. It was found that at least three complexes: diamine complex [Rh(L2)2]+ TfO-, solvate complex [Rh(L1)2(solv)2]+ TfO-, and diamine-bis-phosphine complex [Rh(L1)2L2]+ TfO- may be catalytic precursors. 相似文献
6.
N-Sulfinyltrifluoromethanesulfonamide CF3SO2N=S=O reacts with salicylaldehyde, 2-furaldehyde, 2-thiophenecarbaldehyde, 3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde, and 2-phenyl-2H-1,2,3-triazole-4-carbaldehyde to afford the corresponding N-aryl(hetaryl)methylidenetrifluoromethanesulfonamides in high yields. Reactions of the latter with aniline give no adducts at the C=N bond but transamination products. The reaction of trifluoromethanesulfonamide with phenyl isocyanate led to formation of N,N′-diphenylurea instead of expected N-phenyl-N′-(trifluoromethylsulfonyl)urea.__________Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 7, 2005, pp. 1006–1010.Original Russian Text Copyright © 2005 by Shainyan, Tolstikova. 相似文献
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2-Phenyl-4-trifluoromethylsulfonylmethyl-2H-1,2,3-triazole was synthesized from 4-bromo-methyl-2-phenyl-2H-1,2,3-triazole and sodium trifluoromethanesulfinate CF3SO2Na. 1(2)-Ethyl-4-nitro-1(2)H-1,2,3-triazoles and 4-nitro-2-phenyl-2H-1,2,3-triazole were reduced to the corresponding amines. Intermediate 1,2-bis(1-ethyl-1H-1,2,3-triazol-4-yl)diazene 1-oxide exists as a mixture of syn and anti isomers, the former being stabilized via formation of a strong intramolecular hydrogen bond. The reduction of 2-ethyl-4-nitro-2H-1,2,3-triazole in the presence of HCl afforded the target 4-amino-2-ethyl-2H-1,2,3-triazole and also 4-amino-5-chloro-2-ethyl-2H-1,2,3-triazole. Treatment of alkyl-substituted 4-amino-1,2,3-triazoles with trifluoromethanesulfonyl chloride and pentafluoroethanesulfonyl chloride gave N-triazolyl-substituted trifluoromethane- and pentafluoroethanesulfonamides and -imides. 相似文献
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Russian Journal of Organic Chemistry - Ethynyl(trimethyl)silane reacted with N,N-dichloroarenesulfonamides to give unstable N-[2,2-dichloro-2-(trimethylsilyl)ethylidene]arenesulfonamides... 相似文献
10.
L. L. Tolstikova I. V. Sterkhova B. A. Shainyan 《Russian Journal of Organic Chemistry》2014,50(9):1247-1251
Urea and thiourea form complexes with trifluoromethanesulfonic acid, its monohydrate, and lithium salt CF3SO3Li. Urea complexes with trifluoromethanesulfonic acid are also formed as a result of hydrolysis in the reaction of N,N′-bis(trimethylsilyl)carbodiimide or cyanamide with trifluoromethanesulfonic acid in water. 相似文献