Синтез и свойства 4-замещенных 5Н-123-дитиазолов (стр. 26 из 26)

56. Besson T., Emayan K., Rees C. W. /1,2,3-Dithiazoles and new routes to 3,l-benzoxazin-4-ones, 3,l -benzothiazin-4-ones and N-arylcyanothioformamides / J. Chem. Soc., Perkin Trans. 1, 1995, 2097 - 2102.

57. Cottenceau G., Besson T., Gautier V., Rees C. W., Pons A.-M. /Antibacterial evaluation of novel N-arylimino-1,2,3-dithiazoles and N-arylcyanothioformamidines/ Bioorg. Med. Chem. Lett., 1996, 6, 529 - 532.

58. Lee H.-S., Kim K. /Reactions of 5-arylimino-4-chloro-5H-1,2,3-dithiazoles with stable phosphoranes: Novel preparation of dithiomethylenephosphoranes/ Tetrahedron Lett., 1996, 37, 869 - 872.

59. Besson T., Guillard J., Rees C. W., Thiery V. /New syntheses of aryl isothiocyanates/ J. Chem. Soc., Perkin Trans. 1, 1998, 889 - 892.

60. Iwakawa T., Murabayashi A. /New Synthesis of 5-Cyano-1,2,4-thiadiazoles/ Heterocycles, 1999, 51, 811 - 819.

61. Oh K. C., Lee H., Kim K. /A facile synthesis of N′-(p-toluenesulfonyl)-N-alkyl- and N,N-dialkylcyanoformamidines and 1,3-dialkyl-2-(p-toluenesulfonyl)guanidines / Tetrahedron Lett., 1993, 33, 4963 - 4966.

62. Lee H., Kim K. /Reactions of 5-(Arylimino)-4-chloro-5H-1,2,3-dithiazoles with Primary and Secondary Alkylamines: Novel Synthesis of (Ary1imino)cyanomethyl Alkylamino Disulfides and Their Mechanisms of Formation/ J. Org. Chem., 1993, 58, 7001 - 7008.

63. Lee H., Kim K., Whang D., Kim K. /Novel Synthesis of 5-(Arylimino)-4-(dialkylamino)-5H-l,2,3-dithiazoles and the Mechanism of Their Formation/ J. Org. Chem., 1994, 59, 6179 - 6183.

64. L’abbe G., D’hooge B., Dehaen W. / Unusual behaviour of 4,5-dichloro-1,2,3-dithiazolium chloride (Appel's salt) with 5-aminopyrazoles: a synthetic method of 1H-pyrazolo[3,4-d]thiazoles / J. Chem. Soc., Perkin Trans. 1, 1995, 2379 - 2380.

65. Konstantinova L. S., Rakitin O. A., Rees C. W., Sivadasan S., Torroba T. / New route to 2-cyanobenzimidazoles / Tetrahedron, 1998, 54, 9639 - 9650.

66. Lee H.-S., Chang Y.-G., Kim K. /A facile synthesis of 3-substituted 2-cyanoquinazolin-4(3H)-ones and 3-alkyl-2-cyanothieno[3,2-d]pyrimidin-4(3H)-ones via 1,2,3-dithiazoles/ J. Heterocycl. Chem., 1998, 35, 659 - 668.

67. Mohanta P. K., Kim K. /New Synthetic Route to Tetracyclic Quinazolin-4(3H)-one Ring System/ Heterocycles, 2002, 57, 1471 - 1485.

68. Jeon M.-K., Kim D.-S., La H. J., Ha D.-C., Gong Y.-D. /Solid-phase synthesis of 2-cyanoquinazolin-4(3H)-one and 2,3-dihydrooxazolo[2,3-b]quinazolin-5-one derivatives utilizing resin-bound anthranilic acid derivatives/ Tetrahedron Lett., 2005, 46, 7477 - 7481.

69. Chang Y.-G., Kim K. /Synthesis of 3-Aryl-3,4-dihydro-4-hydroxy-4-phenylquinazoline-2- carbonitrile via 2-(Benzoyl)arylimino-4-chloro-5H-1,2,3-dithiazoles/ Synlett, 2002, 1423 - 1426.

70. de Pereira F. M., Alexandre F. R., Thiery V., Besson T. /A rapid and convenient synthesis of novel 1-imino-2,3-dihydro-1Hpyrazino [2,1,-b]quinazolin-5-ones/ Tetrahedron Lett., 2004, 45, 3097 - 3099.

71. de Pereira F. M., Thiery V., Besson T. /Unexpected formation of aryl dialkyl carbinol as a side product from the reaction of methoxyarylaldehydes with Grignard reagents / Tetrahedron, 2006, 63, 847 - 851.

72. de Pereira F. M., Thiery V., Besson T. /Synthesis of novel 2,3-condensed thieno[2,3-d]pyrimidin-4-ones via Appel's salt chemistry/ J. Sulfur Chem., 2005, 27, 49 - 55.

73. Besson T., Dozias M.-J., Guillard J., Jacquault P., Legoy M.-D., Rees C. W. /Expeditious routes to 4-alkoxyquinazoline-2-carbonitriles and thiocarbamates via N-arylimino-1,2,3-dithiazoles using microwave irradiation / Tetrahedron, 1998, 54, 6475-6484.

74. Chang Y.-G., Kim K. /A Facile Synthesis of N-Arylcyanoformamidoximes, 4-Aryl-3-cyano-1,2,4-oxadiazin-5(6H)-ones, 2-Cyanoquinazoline-3-oxides, and 2-Cyanoquinazolines via 5-Arylimino-4-chloro-5H-1,2,3-dithiazoles / Heterocycles, 1999, 51, 2653-2666.

75. Besson T., Rees C. W. /Some chemistry of 4,5-dichloro-l,2,3-dithiazolium chloride and its derivatives/ J. Chem. Soc., Perkin Trans. 1, 1995, 1659-1662.

76. Frere S., Thiery V., Besson T. /Eco-Friendly Microwave-Assisted Scaleable Synthesis of 2-Cyanobenzothiazoles via N-Arylimino-1,2,3-dithiazoles/ Synth. Commun., 2003, 33, 3795-3804.

77. Besson T., Dozias M.-J., Guillard J., Rees C. W. /New route to 2-cyanobenzothiazoles via N-arylimino-1,2,3-dithiazoles/ J. Chem. Soc., Perkin Trans. 1, 1998, 3925-3926.

78. Beauchard A., Chabane H., Sinbandhit S., Guenot P., Thiery V., Besson T. /Synthesis of original thiazoloindolo[3,2-c]quinoline and novel 8-N-substituted-11H-indolo[3,2-c]quinoline derivatives from benzotriazoles. Part I/ Tetrahedron, 2006, 62, 1895-1903.

79. Testard A., Loge C., Leger B., Robert J.-M., Lozach O., Blairvacq M., Meijer L., Thiery V., Besson T. /Thiazolo[5,4-f]quinazolin-9-ones, inhibitors of glycogen synthase kinase-3/ Bioorg. Med. Chem. Lett., 2006, 16, 3419-3423.

80. Testard A., Picot L., Lozach O., Blairvacq M., Meijer L., Murillo L., Piot J.-M., Thiery V., Besson T. /Synthesis and evaluation of the antiproliferative activity of novel thiazoloquinazolinone kinases inhibitors/ J. Enzyme Inhibition Med. Chem., 2005, 20, 557-568.

81. Rees C. W., Roe D. G., Thiery V. /Imidazoquinolinethiones from quinolines: a new molecular rearrangement/ J. Chem. Soc., Chem. Commun., 1996, 2775-2776.

82. Besson T., Rees C. W., Roe D. G., Thiery V. /Imidazoquinolinethiones from 8-aminoquinolines by a novel peri-participation/ J. Chem. Soc., Perkin Trans. 1, 2000, 555-561.

83. Cuadro A. M., Alvarez-Builla J. /4,5-Dichloro-1,2,3-dithiazolium chloride (Appel's Salt): Reactions with N-nucleophiles/ Tetrahedron, 1994, 50, 10037-10046.

84. Lee H., Kim K. /A new procedure to N-arylcyanothioformamidines from 5-arylimimino-4-chloro-5H-1,2,3-dithiazoles/ Bull. Korean Chem. Soc., 1992, 13, 107-108.

85. Besson T., Rees C. W., Thiery V. /Convenient Synthesis of Dithiooxamides from N-Arylimino-1,2,3-dithiazoles/ Synthesis, 1999, 1345-1348.

86. Kim K. / Recent Advances in 1,2,3-Dithiazole Chemistry/ Phosphorus, Sulfur, Silicon Related Elem., 1997, 120-121, 229-244.

87. Chang Y.-G., Lee H.-S., Kim K. /A convenient synthesis of symmetrical N,N-dialkylureas by the reactions of 4-chloro-5H-1,2,3-dithiazol-5-one with alkylamines/ Tetrahedron Lett., 2001, 42, 8197-8200.

88. Park Y. S., Kim K. /4-Chloro-5H-1,2,3-dithiazol-5-one: a good α-thiocyanating agent for α,β-unsaturated β-amino esters/ Tetrahedron Lett., 1999, 40, 6439-6442.

89. Lee H.-S., Kim K. /Reactions of 4-chloro-5H-1,2,3-dithiazol-5-thione with primary and secondary alkylamines: Novel method for preparing N-alkyl- and N,N-dialkylcyanothioformamides/ Tetrahedron Lett., 1996, 37, 3709-3712.

90. Chang Y.-G., Kim K. / Reactions of 4-chloro-5H-1,2,3-dithiazole-5-thione with alpha,beta-unsaturated beta-amino esters: Formation of 2-[2-(1-alkenylsulfanyl-1-alkoxycarbonyl-2-amino)-1,2-dicyano-vinylsulfanyl]-3-amino-2-alkenoic alkyl esters/ J. Heterocycl. Chem., 2002, 39, 29-35.

91. Koutentis P. A., Rees C. W., White A. J. P., Williams D. J. /Conversion of a 1,2,3-dithiazole into a 3H-pyrrole-3-thione and a 3H-pyrrol-3-ylidenephosphorane / J. Chem. Soc., Perkin Trans. 1, 1998, 2765-2769.

92. Lee H.-S., Kim K. /Formation of 2,5-dihydro-2-iminopyrroles, 2,5-dihydro-2-iminofurans and (Z)-3-alkylamino-2,3-dicyanoacrylatesvia4-chloro-5H-1,2,3-dithiazol-5-ylidene derivatives/ Tetrahedron Lett., 1998, 39, 6895-6898.

93. Jeon M.-K., Kim K. /Reactions of 5-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)-2,2- dimethyl-1,3-dioxane-4,6-dione with primary and secondary alkylamines / J. Chem. Soc., Perkin Trans. 1, 2000, 3107-3112.

94. Koutentis P. A., Rees C. W. /Reaction of Herz salts with malononitrile: a general route to (6H-1,2,3-benzodithiazol-6-ylidene)malononitriles/ J. Chem. Soc., Perkin Trans. 1, 2002, 315-319.

95. Brusso J. L., Derakhshan S., Itkis M. E., Kleinke H., Haddon R. C., Oakley R. T., Reed R. W., Richardson J. F., Robertson C. M., Thompson L. K. /Isostructural Bisdithiazolyl and Bisthiaselenazolyl Radicals: Trends in Bandwidth and Conductivity / Inorg. Chem., 2006, 45, 10958-10966.

96. Barclay T. M., Cordes A. W., Oakley R. T., Preuss K. E., Reed R. W. /1,1A,2,2A,3,3A-Tetrathiadiazafulvalenes, preparation and characterisation of trans-[ClCNS₂CNCS₂NCCl]/ J. Chem. Soc., Chem. Commun., 1998, 1039-1040.

97. Beer L., Brusso J. L., Cordes A. W., Haddon R. C., Itkis M. E., Kirschbaum K., MacGregor D. S., Oakley R. T., Pinkerton A. A., Reed R. W. / Resonance-Stabilized 1,2,3-Dithiazolo-1,2,3-dithiazolyls as Neutral .-Radical Conductors / J. Am. Chem. Soc., 2002, 124, 9498-9509.

98. Oakley R. T., Reed R. W., Robertson C. M., Richardson J. F. /Naphthalene-1,2,3-Dithiazolyl and Its Selenium-Containing Variants/ Inorg. Chem., 2005, 44, 1837 - 1845.

99. Zhivonitko V. V., Makarov A. Yu., Bagryanskaya I. Yu., Gatilov Y. V., Shakirov M. M., Zibarev A. V. /New Polysulfur-Nitrogen Heterocycles by Thermolysis of 1,3λ4δ2,2,4-Benzodithiadiazines in the Hydrocarbon and Fluorocarbon Series/ Eur. J. Inorg. Chem., 2005, 4099 - 4108.

100. Plater M. J., Rees C. W. /Organic Heterocyclothiazenes. Part 15.' Pyrazolotrithiadiazepines and Their Rearrangement to 1,2,3-Dithiazoles/ J. Chem. Soc., Perkin Trans. 1, 1991, 311 - 316.

101. Kaszynski P. /Theoretical Analysis of Heteroaromatic Thioaminyl Radicals. Part 1: A Comparison of Ab Initio and Density Functional Methods in Calculations of Molecular Geometry and Isotropic Hyperfine Coupling Constants/ J. Phys. Chem. (A), 2001, 105, 7615 - 7625.

102. Kaszynski P. /Theoretical Analysis of Heteroaromatic Thioaminyl Radicals. Part 2: A Comparison of Ab Initio and Density Functional Methods in the Description of Redox Processes/ J. Phys. Chem. (A), 2001, 105, 7626 - 7633.

103. Thiery V., Rees C. W., Besson T., Cottenceau G., Pons A.-M. /Antimicrobial activity of novel N-quinolinyl and N-naphthylimino-1,2,3-dithiazoles/ Eur. J. Med. Chem., 1998, 33, 149-153.

104. Baraldi P. G., Pavani M. G., del C. Nunez M., Brigidi P., Vitali B., Gambari R., Romagnoli R. /Antimicrobial and Antitumor Activity of N-Heteroimmine-1,2,3-dithiazoles and Their Transformation in Triazolo-, Imidazo-, and Pyrazolopirimidines/ Bioorg. Med. Chem., 2002, 10, 449 - 456.

105. Besson T., Rees C. W., Cottenceau G., Pons A.-M. /Antimicrobial evaluation of 3,1-benzoxazin-4-ones, 3,1-benzothiazin-4-ones, 4-alkoxyquinazolin-2-carbonitriles and N-arylimino-1,2,3-dithiazoles/ Bioorg. Med. Chem. Lett., 1996, 6, 2343 - 2348.

106. Jurgen F., Hartmut S., Roland M. /1,2-Dithiolthione-(3) (Tritione) aus 3-Chlor-1,2- dithioliumsalzen und schwefelfreien Basen/ Z. Chem. 1967, 7, 275.

107. Смоленцев А.А. /Синтез и свойства функционально замещенных 1,2-дитиолов./ Диссертация на соискание степени кандидата химических наук. ИОХ РАН. Москва, 2005.

108. Masuda K., Adachi J., Nomura K. /Studies on mesoionic compounds. Part 10. Synthesis and chemical properties of mesoionic 1,2,5-thiadiazolium-3-olates/ J. Chem. Soc., Perkin Trans. 1: 1981, 1033 – 1036.

109. Goldish D., Axon B. W., Moore H., W. /Cyanoketenes. Cycloadditions of tert-Butylcyano- and Chlorocyanoketene to Sulfer Diimides/ Heterocycles, 1983, 2, 187 – 192.

110. Lunn W. H. W., Shadle J. K. / Facile synthesis of 3-oxo-1,2,5-thiadiazoles; 7β-

(3-oxo-1,2,5-thiadiazol-2-yl) cephalosporins/ Tetrahedron, 1992, 48, 8615 – 8620.

111. Ross J., M., Smith W.C. /Hydroxy-1,2,5-thiadiazoles. I. A Novel Route from Potassium Cyanide and Sulfur Dioxide/ J. Amer. Chem. Soc., 1964, 86, 2861 – 2868.

112. Ладилина Е. Ю., Семенов В. В., Курский Ю. А., Хоршев С. Я., Домрачеев Г. А. /Реакция первичных аминов с тетрацианоэтиленом/ Журн. орг. химии., 2004, 9, 1308 - 1311.

113. Заварзин И.В., Яровенко В.Н., Чернобурова Е.И., Краюшкин М.М. /Синтез монотиоксамидов/ Изв. АН, Сер. хим., 2004, 2, 398 - 401.

114. Maliverney C., Viehe H. G. /Trifluoropyruvic and lactic thioamides from ethyl trifluoroacetoacetate/ Tetrahedron Lett., 1990, 44, 6339 - 6342.

115. Fumio T., Hisakazu M., Hideko K., Urbanczyk-Lipkowska Z. /Chiral Arrangement of N-Ethyl-N-isopropylphenylglyoxylamide Molecule in Its Own Crystal and in an Inclusion Crystal with a Host Compound and Their Photoreactions in the Solid State That Give Optically Active -Lactam Derivatives/ J. Org. Chem. 1997, 62, 9261 - 9266.

116. Matsumoto K., Hashimoto S., Uchida T., Okamoto T., Otani S. /Direct aminolysis of nonactivated and thermally unstable esters at high pressure/ Chem. Ber., 1989, 122, 1357 – 1364.

117. Firouz M., Mirjafary M., Saeidian Z., Javan H., Jebeli M. /A Facile Aerobic Copper-Catalyzed α-Oxygenation of Aryl Thioacetamides: An Efficient Access to α-Keto Aryl Thioamides/ Synlett, 2008, 6, 892 – 896.

118. Dell'Erba C., Novi M., Petrillo G., Tavani C. /Electrophilicα-p-tolylhydrazonylation of tert-butyl alkanoates and tertiary alkanamides with tert-butylp-tolylazo sulfide/ Tetrahedron, 1996, 52, 5889 – 5898.

119. Iizuka M., Kondo Y. /Remarkable ligand effect on the palladium-catalyzed double carbonylation of aryl iodides/ Chem. Commun., 2006, 16, 1739 – 1741.

120. Evans D. A., Weber A. E. /Synthesis of the cyclic hexapeptide echinocandin D. New approaches to the asymmetric synthesis of .beta.-hydroxy .alpha.-amino acids/ J. Amer. Chem. Soc., 1987, 109, 7151- 7157.

121. Sakai S., Kominami M., Chonan K., Enomoto T., Fujinami T. /A New Method for Preparation of Tetraalkyl Orthocarbonates from Sodium Alkoxides, Tetrachlorostannane, and Carbon Disulfide/ Synthesis, 1984, 3, 233–234.

122. Shibuya I., Katoh E., Gama Y., Oishi A., Taguchi Y., Tsuchiya T. /Acetal Formation by Metal Ion-mediated Desulfurization-Condensation of Thioketones with Diols and Phenols/ Heterocycles, 1996, 43, 851 – 860.

123. Oishi, T., Mori M., Ban Y. / Activation of Weak Organic Bases. V. The Alkylation of Thiono Esters by Diethoxycarbonium Hexachloroantimonate [chemical formula], SbCl₆/ Chem. Pharm. Bull., 1971, 19, 1871–1875.

124. Morgenstern J., Mayer R. /Organische Schwefelverbindungen. 63. Zur Chemie des Thiocyclohexanons/ J. Prakt. Chem.; 1966, 34, 116 138.

125. Hanusek J., Sedlak M., Keder R., Sterba V. /Kinetics and Mechanism of Desulfurization Reaction of 1-Methyl-2-phenylquinazoline-4(1H)-thiones/ Coll. Czech. Chem. Comm., 2004, 69, 2212-2222.

126. Okazaki R., Inoue K., Inamoto N. // Synthesis of 5H-1,2,3-Dithiazole, a Novel Heterocycle/ Heterocycles, 1981, 15, 803 – 806.

127. Shimizu H., Murakami M. /Synthesis of

-keto esters by the rhodium-catalysed reaction of cyanoformate with arylboronic acids/ Chem. Commun., 2007, 27, 2855 – 2857.

128. Makosza M., Sienkiewicz K., Wojciechowski K. /Vicarious Nucleophilic Substitution of Hydrogen in Nitroarenes by Carbanions of Alkyl Dichloroacetates. Some New Transformations of Chloro(nitroaryl)acetates/ Synthesis, 1990, 9, 850 – 852.

129. Dahn H., Pechy P., Toan V. V. /¹⁷O NMR Spectra of Carbonyl Compounds ArCOX: Influence of Groups X on the Polarity of the Carbonyl Group/ Magn. Reson. Chem., 1997, 35, 589 – 592.

130. Meng Q., Sun Y., Ratovelomanana-Vidal V. G. Jean Pierre Z. Z. /CeCl₃·7H₂O: An Effective Additive in Ru-Catalyzed Enantioselective Hydrogenation of Aromatic α-Ketoesters/ J. Org. Chem., 2008, 73, 3842 – 3847.

131. Heras M. A., Vaquero J. J., Garcia-Navio J. L., Alvarez-Builla J. /Addition of Grignard Reagents to 1-(N-(Alkoxyoxalyl)-N-methylamino)-3-methylimidazolium Salts: A General Method for -Keto Ester Synthesis/ J. Org. Chem. 1996, 61, 9009-9011.

132. Walter W., Bode K. D. /Über die Oxydationsprodukte von Thiocarbonsäureamiden, XVI. Oxydationsreaktionen an Thiocarbonsäureamiden mit elektronenanziehenden Substituenten am C-Atom/ Liebigs Ann. Chem., 1966, 698, 131 – 144.

133. Furukawa M., Shiraishi K., Hayashi S. /The Conversion of α-Carbonylmethylthiosulfates into Thiocarboxamides/ Chem. Pharm. Bull., 1972, 20, 1921 – 1926.

134. Kagami H., Motoki S. /Nucleophilic substitution on dialkoxy disulfides. Reactions with mercaptans or amines/ J. Org. Chem., 1977, 42, 4139 – 4141.

135. Seyferth D. H., Hui R. C. /High yield acyl anion trapping reactions: direct nucleophilic acylation of isocyanates and isothiocyanates./ Tetrahedron Lett., 1984, 25, 5251 – 5254.

136. Adiwidjaja G., Guenther H., Voss J. /α-Oxo- und α-Thioxothioamide aus Methylketonen/ Liebigs Ann. Chem., 1983, 7, 1116 – 1132.

137. Katritzky A. R., Feng D., Qi M. /Synthesis of β-Alkoxy Ketones and α‘-Functionalized β-Alkoxy Ketones Utilizing Benzotriazole-Stabilized Acyl Anion Synthons/ J. Org. Chem., 1998, 63, 1473 – 1477.

138. Walter W., Hell P.-M. /über die Reaktion von Thiocarbonsäureamiden mit Sulfenylchloriden/ Liebigs Ann. Chem., 1969, 727, 22 – 34.

139. Bestmann H. J., Schmid G., Sandmeier D., Schade G., Oechsner H. /Kumulierte Ylide, XIV. Phosphacumulen-Ylide als Cyclisierungsbausteine in der Heterocyclensynthese/ Chem. Ber., 1985, 118, 1709 – 1719.

140. Lu Z. E., Sun D. Q., Xu T. L., W. Jun, Xu L. C., Chen K. Q. /New Heterocycles Forming Reactions of Acyl Thioformanilides/ Org. Prep. Proc. Int., 1992, 24, 358 – 362.

141. Mu X., Zou J., Zeng R., Wu J. /Mn(III)-Promoted cyclization of substituted thioformanilides under microwave irradiation: a new reagent for 2-substituted benzothiazoles/ Tetrahedron Lett., 2005, 46, 4345 – 4348.

142. Bong R. C., Hak S. C., Nam S. C. /Elimination Reactions of (E)- and (Z)-Benzaldehyde O-Benzoyloximes. Transition State Differences for the Syn- and Anti-Eliminations Forming Nitriles/ J. Org. Chem., 1998, 63, 4685 – 4690.

143. Coppola G.M., Damon R. E. /Acetylenic Amides. Generation and Reactions of Dianions Derived from 2-Propynamides/ J. Heterocyclic Chem., 1995, 32, 1133 - 1139.

144. Campaigne E., Skowronski G., Rogers R. B. /Synthesis of β-Dimethylaminoethyl and α-Hydroxy-β-Dimethylaminoethyl Derivatives from Organolithium Compounds and Tetramethyoxamide/ Synth. Commun., 1973, 3, 325 – 332.

145. Klaus F, Mohebullah Z. /Diels-alder-reaktionen mit cyanthioformamiden/ Tetrahedron Lett., 1977, 18, 2139-2140.