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Volumn 36, Issue 15, 2006, Pages 2087-2095

Formation of 1,2,5-oxadiazole, isoxazole, isothiazole, 1,2,3-triazole, and pyrrole rings from N-(5,5-dimethyl-3-oxocyclohexenyl)-S,S-diphenylsulfilimine

Author keywords

1,2,3 triazole; 1,2,5 oxadiazole; Isothiazole; Isoxazole; Pyrrole; Sulfilimine

Indexed keywords

1,2,3 TRIAZOLE DERIVATIVE; FURAZAN DERIVATIVE; ISOTHIAZOLE DERIVATIVE; ISOXAZOLE DERIVATIVE; N (5,5 DIMETHYL 3 OXOCYCLOHEXENYL)DIPHENYLSULFILIMINE; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33745413297     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910600636436     Document Type: Article
Times cited : (3)

References (17)
  • 1
    • 0000667483 scopus 로고    scopus 로고
    • Sulfimides: Applications in stereoselective synthesis
    • Reviews on sulfilimines (a) Taylor, P. C. Sulfimides: Applications in stereoselective synthesis. Sulfur Reports 1999, 21, 241-280;
    • (1999) Sulfur Reports , vol.21 , pp. 241-280
    • Taylor, P.C.1
  • 2
    • 33847089781 scopus 로고
    • The chemistry of sulfilimines
    • (b) Gilchrist, T. L.; Moody, C. J. The chemistry of sulfilimines. Chem. Rev. 1977, 77, 409-435;
    • (1977) Chem. Rev. , vol.77 , pp. 409-435
    • Gilchrist, T.L.1    Moody, C.J.2
  • 3
    • 57249085578 scopus 로고    scopus 로고
    • Sulfur ylides in the synthesis of heterocyclic and carbocyclic compounds
    • (c) Lakeev, S. N.; Maydanova, I. O.; Galin, F. Z.; Tolstikov, G. A. Sulfur ylides in the synthesis of heterocyclic and carbocyclic compounds. Russian Chem. Rev. 2001, 70, 655-672;
    • (2001) Russian Chem. Rev. , vol.70 , pp. 655-672
    • Lakeev, S.N.1    Maydanova, I.O.2    Galin, F.Z.3    Tolstikov, G.A.4
  • 4
    • 0001753559 scopus 로고
    • Advances in the chemistry of sulfimides and related compounds
    • (d) Koval, I. V. Advances in the chemistry of sulfimides and related compounds. Sulfur Reports 1993, 14, 149-221.
    • (1993) Sulfur Reports , vol.14 , pp. 149-221
    • Koval, I.V.1
  • 5
    • 0037049302 scopus 로고    scopus 로고
    • Ring closure reactions of β-nitroso-, β-acyl-, and β-thiocarbamoyl-α, β-unsaturated sulfilimines. Synthesis of [1,2,5]oxadiazolo[3,4-d]-, isoxazolo[3,4-d]-, and isothiazolo[3,4-d]pyrimidines from uracil
    • Matsumoto, N.; Takahashi, M. Ring closure reactions of β-nitroso-, β-acyl-, and β-thiocarbamoyl-α, β-unsaturated sulfilimines. Synthesis of [1,2,5]oxadiazolo[3,4-d]-, isoxazolo[3,4-d]-, and isothiazolo[3,4-d]pyrimidines from uracil. Tetrahedron 2002, 58, 10073-10079.
    • (2002) Tetrahedron , vol.58 , pp. 10073-10079
    • Matsumoto, N.1    Takahashi, M.2
  • 6
    • 0345282997 scopus 로고    scopus 로고
    • Synthesis of 2H-1,2,3-triazolo[4,5-d]pyrimidine-5,7-diones from uracils using cyclization reactions of β-azo-α, β-unsaturated sulfilimines
    • Matsumoto, N.; Takahashi, M. Synthesis of 2H-1,2,3-triazolo[4,5-d] pyrimidine-5,7-diones from uracils using cyclization reactions of β-azo-α, β-unsaturated sulfilimines. Heterocycles 2003, 60, 2677-2684.
    • (2003) Heterocycles , vol.60 , pp. 2677-2684
    • Matsumoto, N.1    Takahashi, M.2
  • 7
    • 22144491936 scopus 로고    scopus 로고
    • Synthesis of pyrrolo[2,3-d]pyrimidine-2,4-diones by sunlight photolysis of N-(5-vinyluracil-6-yl)sulfilimines
    • Matsumoto, N.; Takahashi, M. Synthesis of pyrrolo[2,3-d]pyrimidine-2,4- diones by sunlight photolysis of N-(5-vinyluracil-6-yl)sulfilimines. Tetrahedron Lett. 2005, 46, 5551-5554.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 5551-5554
    • Matsumoto, N.1    Takahashi, M.2
  • 8
    • 2942568249 scopus 로고    scopus 로고
    • Synthesis of heterocycles from alkyl 3-(dimethylamino)propenoates and related enaminones
    • Reviews on enaminoketones: (a) Stanovnik, B.; Svete, J. Synthesis of heterocycles from alkyl 3-(dimethylamino)propenoates and related enaminones. Chem. Rev. 2004, 104, 2433-2480;
    • (2004) Chem. Rev. , vol.104 , pp. 2433-2480
    • Stanovnik, B.1    Svete, J.2
  • 9
    • 4344710140 scopus 로고    scopus 로고
    • Recent development in preparation, reactivity and biological activity of enaminoketones and enaminothiones and their utilization to prepare heterocyclic compounds
    • (b) Negri, G.; Kascheres, C.; Kascheres, A. J. Recent development in preparation, reactivity and biological activity of enaminoketones and enaminothiones and their utilization to prepare heterocyclic compounds. J. Heterocycl. Chem. 2004, 41, 461-491;
    • (2004) J. Heterocycl. Chem. , vol.41 , pp. 461-491
    • Negri, G.1    Kascheres, C.2    Kascheres, A.J.3
  • 10
    • 0141619395 scopus 로고    scopus 로고
    • Recent developments in the chemistry of enaminones
    • (c) Elassar, A.-Z. A.; El-Khair, A. A. Recent developments in the chemistry of enaminones. Tetrahedron 2003, 59, 8463-8480;
    • (2003) Tetrahedron , vol.59 , pp. 8463-8480
    • Elassar, A.-Z.A.1    El-Khair, A.A.2
  • 12
    • 0010790147 scopus 로고
    • Vilsmeier reagents: Preparation of β-halo-α,β-unsaturated ketones
    • Mewshaw, R. E. Vilsmeier reagents: Preparation of β-halo-α, β-unsaturated ketones. Tetrahedron Lett. 1989, 30, 3753-3756.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 3753-3756
    • Mewshaw, R.E.1
  • 13
    • 0001215371 scopus 로고
    • Reactions of N-unsubstituted arylsulfilimines with acylating agents and with activated halobenzenes, alkynes, and alkenes
    • Tamura, Y.; Sumoto, R.; Matsushima, H.; Taniguchi, H.; Ikeda, M. Reactions of N-unsubstituted arylsulfilimines with acylating agents and with activated halobenzenes, alkynes, and alkenes. J. Org. Chem. 1973, 38, 4324-4328.
    • (1973) J. Org. Chem. , vol.38 , pp. 4324-4328
    • Tamura, Y.1    Sumoto, R.2    Matsushima, H.3    Taniguchi, H.4    Ikeda, M.5
  • 15
    • 11144337201 scopus 로고    scopus 로고
    • Formation of pyridazinium salts by azo coupling of N-substituted 3-amino-1-phenylbut-2-en-1-ones and diazoniumu salts
    • Šimůnek, P.; Pešková, M.; Bertolasi, V.; Lyčka, A.; Macháček, V. Formation of pyridazinium salts by azo coupling of N-substituted 3-amino-1-phenylbut-2-en-1-ones and diazoniumu salts. Eur. J. Org. Chem. 2004, 5055-5063.
    • (2004) Eur. J. Org. Chem. , pp. 5055-5063
    • Šimůnek, P.1    Pešková, M.2    Bertolasi, V.3    Lyčka, A.4    Macháček, V.5
  • 16
    • 43949153832 scopus 로고
    • β-Ethoxyvinyl polyfluoroalkyl ketones - Versatile synthones in fluoroorganic chemistry
    • (a) Gerus, I. I.; Gorbunova, M. G.; Kukhar, V. P. β-Ethoxyvinyl polyfluoroalkyl ketones - versatile synthones in fluoroorganic chemistry. J. Fluorine Chem. 1994, 69, 195-198;
    • (1994) J. Fluorine Chem. , vol.69 , pp. 195-198
    • Gerus, I.I.1    Gorbunova, M.G.2    Kukhar, V.P.3
  • 17
    • 0001848439 scopus 로고
    • Electrophilic substitutions of olefinic hydrogens, II: Acylation of vinyl ethers and N-vinyl amides
    • (b) Hojo, M.; Masuda, R.; Kokuryo, Y.; Shioda, H.; Matsuo, S. Electrophilic substitutions of olefinic hydrogens, II: Acylation of vinyl ethers and N-vinyl amides. Chem. Lett. 1976, 499-502.
    • (1976) Chem. Lett. , pp. 499-502
    • Hojo, M.1    Masuda, R.2    Kokuryo, Y.3    Shioda, H.4    Matsuo, S.5


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