메뉴 건너뛰기




Volumn 15, Issue 2, 2010, Pages 997-1006

Synthesis of 1-(4-trifluoromethoxyphenyl)-2,5-dimethyl-3-(2-rthiazol-4-yl)- 1H-pyrroles via chain heterocyclization

Author keywords

Chain heterocyclization; Fluorinated heterocycles; Paal Knorr reaction; Trifluoromethoxy group

Indexed keywords

PYRROLE DERIVATIVE;

EID: 77649220554     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules15020997     Document Type: Article
Times cited : (7)

References (24)
  • 1
    • 17744417463 scopus 로고    scopus 로고
    • Chemistry and biology of roseophilin and the prodigiosin alkaloids: A survey of the last 2500 years
    • Fürstner, A. Chemistry and biology of roseophilin and the prodigiosin alkaloids: A survey of the last 2500 years. Angew. Chem. Int. Ed. 2003, 42, 3582-3603.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 3582-3603
    • Fürstner, A.1
  • 2
    • 0035686992 scopus 로고    scopus 로고
    • Four new bioactive pyrrole-derived alkaloids from the marine sponge Axinella brevistyla
    • Tsukamoto, S.; Tane, K.; Ohta, T.; Matsunaga, S.; Fusetani, N.; van Soest, R.W.M. Four new bioactive pyrrole-derived alkaloids from the marine sponge Axinella brevistyla. J. Nat. Prod. 2001, 64, 1576-1978.
    • (2001) J. Nat. Prod. , vol.64 , pp. 1576-1978
    • Tsukamoto, S.1    Tane, K.2    Ohta, T.3    Matsunaga, S.4    Fusetani, N.5    Van Soest, R.W.M.6
  • 3
    • 33748806602 scopus 로고    scopus 로고
    • Oxocyclostylidol an intramolecular cyclized oroidin derivative from the marine sponge Stylissa caribica
    • Grube, A.; Köck, M. Oxocyclostylidol, an intramolecular cyclized oroidin derivative from the marine sponge Stylissa caribica. J. Nat. Prod. 2006, 69, 1212-1214.
    • (2006) J. Nat. Prod. , vol.69 , pp. 1212-1214
    • Grube, A.1    Köck, M.2
  • 4
    • 33747139387 scopus 로고    scopus 로고
    • Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl group on adjacent positions
    • Bellina, F.; Rossi, R. Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl group on adjacent positions. Tetrahedron 2006, 62, 7213-7256.
    • (2006) Tetrahedron , vol.62 , pp. 7213-7256
    • Bellina, F.1    Rossi, R.2
  • 5
    • 33847770688 scopus 로고    scopus 로고
    • New pyrrole inhibitors of monoamine oxidase: Synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity
    • La Regina, G.; Silvestri, R.; Artico, M.; Lavecchia, A.; Novellino, E.; Befani, O.; Turini, P.; Agostinelli, E. New pyrrole inhibitors of monoamine oxidase: Synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity. J. Med. Chem. 2007, 50, 922-931.
    • (2007) J. Med. Chem. , vol.50 , pp. 922-931
    • La Regina, G.1    Silvestri, R.2    Artico, M.3    Lavecchia, A.4    Novellino, E.5    Befani, O.6    Turini, P.7    Agostinelli, E.8
  • 8
    • 77649218871 scopus 로고
    • Neue pyrrolderivate und verfahren zu ihrer herstellung
    • Vollenberg, W.; Beckmann, R. Neue pyrrolderivate und verfahren zu ihrer herstellung. Ger. Patent 2427614, 1976.
    • (1976) Ger. Patent 2427614
    • Vollenberg, W.1    Beckmann, R.2
  • 9
    • 33747519634 scopus 로고    scopus 로고
    • Novel small-molecule inhibitors of Anthrax lethal factor identified by high-throughput screening
    • Schepetkin, I.A.; Khlebnikov, A.I; Kirpotina, L.N.; Quinn, M.T. Novel small-molecule inhibitors of Anthrax lethal factor identified by high-throughput screening. J. Med. Chem. 2006, 49, 5232-5244.
    • (2006) J. Med. Chem. , vol.49 , pp. 5232-5244
    • Schepetkin, I.A.1    Khlebnikov, A.I.2    Kirpotina, L.N.3    Quinn, M.T.4
  • 11
    • 17244371011 scopus 로고    scopus 로고
    • α-Fluorinated ethers, thioethers, and amines: Anomerically biased species
    • Leroux, F.; Jeschke, P.; Schlosser, M. α-Fluorinated ethers, thioethers, and amines: Anomerically biased species. Chem. Rev. 2005, 105, 827-856.
    • (2005) Chem. Rev. , vol.105 , pp. 827-856
    • Leroux, F.1    Jeschke, P.2    Schlosser, M.3
  • 12
    • 0036011205 scopus 로고    scopus 로고
    • Blood substitutes and other potential biomedical applications of fluorinated colloids
    • Riess, J.G. Blood substitutes and other potential biomedical applications of fluorinated colloids. J. Fluor. Chem. 2002, 114, 119-126.
    • (2002) J. Fluor. Chem. , vol.114 , pp. 119-126
    • Riess, J.G.1
  • 13
    • 0037071237 scopus 로고    scopus 로고
    • Fluorous micro- and nanophases with a biomedical perspective
    • Riess, J.G. Fluorous micro- and nanophases with a biomedical perspective. Tetrahedron 2002, 58, 4113-4131.
    • (2002) Tetrahedron , vol.58 , pp. 4113-4131
    • Riess, J.G.1
  • 15
    • 78349272412 scopus 로고    scopus 로고
    • Trifluoromethoxy containing azoles and azines: Synthesis and biological activity
    • Gakh, A.A., Kirk, K.L., Eds.; American Chemical Society: Washington, DC, USA
    • Vovk, M.V.; Pinchuk, O.M.; Sukach, V.A.; Tolmachov, A.O.; Gakh, A.A. Trifluoromethoxy Containing Azoles and Azines: Synthesis and Biological Activity. In Fluorinated Heterocycles; Gakh, A.A., Kirk, K.L., Eds.; American Chemical Society: Washington, DC, USA, 2009; pp. 307-345.
    • (2009) Fluorinated Heterocycles , pp. 307-345
    • Vovk, M.V.1    Pinchuk, O.M.2    Sukach, V.A.3    Tolmachov, A.O.4    Gakh, A.A.5
  • 17
    • 77649219225 scopus 로고
    • 4-Phenethylamino pyrimidine derivative, process for preparing the same and agricultural and horticultural chemical for controlling noxious organisms containing the same
    • Obata, T.; Fujii, K.; Ooka, A.; Yamanaka, Y. 4-Phenethylamino pyrimidine derivative, process for preparing the same and agricultural and horticultural chemical for controlling noxious organisms containing the same. Eur. Patent EP0665225, 1995.
    • (1995) Eur. Patent EP0665225
    • Obata, T.1    Fujii, K.2    Ooka, A.3    Yamanaka, Y.4
  • 18
    • 0034485360 scopus 로고    scopus 로고
    • Growth retardants: Effects on gibberellin biosynthesis and other metabolic pathways
    • Rademacher, W. Growth retardants: Effects on gibberellin biosynthesis and other metabolic pathways. Annu. Rev. Plant Physiol. Plant Mol. Biol. 2000, 51, 501-537.
    • (2000) Annu. Rev. Plant Physiol. Plant Mol. Biol. , vol.51 , pp. 501-537
    • Rademacher, W.1
  • 19
    • 0028097839 scopus 로고
    • A controlled trial of Riluzole in amyotrophic lateral sclerosis
    • Bensimon, G.; Lacomblez, L.; Meininger, V. A controlled trial of Riluzole in amyotrophic lateral sclerosis. New Engl. J. Med. 1994, 330, 585-591.
    • (1994) New Engl. J. Med. , vol.330 , pp. 585-591
    • Bensimon, G.1    Lacomblez, L.2    Meininger, V.3
  • 22
    • 33947467139 scopus 로고
    • Friedel-Crafts acylations of 1-phenyl-2,5-dimethylpyrrole and 1,2- diphenyl-5-methylpyrrole
    • Rips, R.; Buu-Hoï, N.P. Friedel-Crafts acylations of 1-phenyl-2,5-dimethylpyrrole and 1,2- diphenyl-5-methylpyrrole. J. Org. Chem. 1959, 24, 551-554.
    • (1959) J. Org. Chem. , vol.24 , pp. 551-554
    • Rips, R.1    Buu-Hoï, N.P.2
  • 23
    • 0007674578 scopus 로고
    • New 2,5-dimethylpyrrole derivatives
    • Bishop, W. S. New 2,5-dimethylpyrrole derivatives. J. Am. Chem. Soc. 1945, 67, 2261-2262.
    • (1945) J. Am. Chem. Soc. , vol.67 , pp. 2261-2262
    • Bishop, W.S.1
  • 24
    • 84980931984 scopus 로고
    • Imidiumazid-hexachloroantimonate (V) mesomeriestabilisierte azide
    • Schmidt, A. Imidiumazid-hexachloroantimonate (V) mesomeriestabilisierte azide. Chem. Ber. 1967, 100, 3319-3325.
    • (1967) Chem. Ber. , vol.100 , pp. 3319-3325
    • Schmidt, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.