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K. A. Frolov V. V. Dotsenko S. G. Krivokolysko V. P. Litvinov 《Russian Chemical Bulletin》2005,54(9):2226-2228
Reactions of (Z)-5-benzylidene-2-thiohydantoin with formaldehyde and primary aromatic amines afforded novel derivatives of imidazo[2,1-b][1,3,5]thiadiazine in 50–69% yields.
Dedicated to Academician N. S. Zefirov on the occasion of his 70th birthday.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 2158–2160, September, 2005. 相似文献
4.
V. V. Dotsenko S. G. Krivokolysko A. N. Chernega V. P. Litvinov 《Russian Chemical Bulletin》2007,56(7):1431-1436
A new stereoselective method for the synthesis of trans-isomers of 2-amino-4-aryl-5-benzoyl-4,5-dihydrothiophene-3-carbonitriles was proposed. The method involves base-catalyzed
reactions of phenacyl thiocyanate with 3-(het)aryl-2-cyanoprop-2-enethioamides. (4R,5S/4S,5R)-2-Amino-5-benzoyl-4-(2-chlorophenyl)-4,5-ihydrothiophene-3-carbonitrile was structurally characterized by X-ray diffraction
analysis.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1379–1383, July, 2007. 相似文献
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V. V. Dotsenko S. G. Krivokolysko V. P. Litvinov 《Chemistry of Heterocyclic Compounds》2007,43(11):1455-1459
5,11-Disubstituted derivatives of 1′-isopropyl-8-thioxospiro[3,5,7,11-tetrazatricyclo[7.3.1.02,7]tridec-2-ene-13,4′-piperidine]-1,9-dicar bonitrile was obtained by the interaction of 10-amino-9-aza-3-azonia-7,11-dicyano-3-isopropylspiro[5,5]undeca-7,10-diene-8-thiolate
with 2 equiv. of a primary amine and excess of formaldehyde. An anomalous reaction product was obtained with o-toluidine — 7,9-dicyano-1′-isopropyl-3-(2-methylphenyl)-1,2,3,4-tetrahydrospiro[pyrido[1,2-a][1,3,5]triazine-8,4′-piper idinium]-6-thiolate.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, 1709–1713, November, 2007. 相似文献
7.
V. V. Dotsenko S. G. Krivokolysko E. B. Rusanov V. P. Litvinov 《Russian Chemical Bulletin》2007,56(7):1437-1440
Reactions of 6-aryl-5-cyano-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidines with formaldehyde and primary amines gave earlier
unknown 3,4-dihydro-2H,6H-pyrimido[2,1-b]-[1,3,5]thiadiazine derivatives in 58–94% yields. In boiling AcOH, these pyrimidothiadiazines underwent the retro-Mannich
reaction leading to the starting pyrimidine-2-thiones. The structure of 3-(4-ethoxyphenyl)-6-oxo-8-phenyl-3,4-dihydro-2H,6H-pyrimido[2,1-b][1,3,5]thiadiazine-7-carbonitrile was studied by X-ray diffraction analysis.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1384–1387, July, 2007. 相似文献
8.
The reactions of N-methylmorpholinium 6-amino-3,5-dicyano-1,4-dihydropyridine-2-thiolates with formaldehyde and primary aromatic amines produce
3,5,7,11-tetraazatricyclo[7.3.1.02,7]tridec-2-ene-1,9-dicarbonitrile derivatives.
For Part 1, see Ref. 1.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2605–2607, November, 2005. 相似文献
9.
Vi. S. Dotsenko 《Theoretical and Mathematical Physics》1992,92(3):938-951
Some elaboration is givent to the structure of physical states in 2D gravity coupled to C1 matter, and to the chiral algebra (w of CM=1 theory which has been found recently, in the continuum approach, by Witten and by Klebanov and Polyakov. It is then shown that the chiral algebra is realized as well in the minimal models of gravity (CM<1), so that it stands as a general symmetry of 2D gravity theories.Dedicated to the memory of the late Professor M. C. PolivanovL. D. Landau Institute of Theortetical Physics, Russian Academy of Sciences. LPTHE, Laboratoire associé No. 280 au CNRS, Universitè Pierre et Marie Curie, Paris VI, France. Published in Teoreticheskaya i Matematicheskaya Fizika, Vol. 92, No. 3, pp. 357–373, September, 1992. 相似文献
10.
K. N. Shavrin V. D. Gvozdev I. Yu. Pinus I. P. Dotsenko O. M. Nefedov 《Russian Chemical Bulletin》2004,53(11):2546-2553
1-Substituted 1-chloro-3-organylthiopropa-1,2-dienes 1a–f belonging to previously unknown type of allenic compounds were synthesized by chlorination of 1-organylthioalk-1-ynes 3a–f with N-chlorosuccinimide. The reactions of compounds 1a–f with ButOK in hexane at –20 °C are accompanied by -elimination of HCl to give new alk-1-ynyl(organylthio)carbenes 2a–f, which add to olefins to form the corresponding 1-(alk-1-ynyl)-1-organylthiocyclopropanes 5 in yields of up to 60%. The electrophilic properties of carbenes 2 were confirmed experimentally.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2440–2447, November, 2004. 相似文献