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Volumn 7, Issue 2, 2010, Pages 172-177

PEG-400 catalyzed reaction for the synthesis of 2, 4, 6-Triarylpyridines and crystal structure of 2,4,6-tris(4'-chlorophenyl)pyridine

Author keywords

2,4,6 Triarylpyridines; Crystal structure; Phase transfer catalyst

Indexed keywords


EID: 77951465396     PISSN: 15701786     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017810790796228     Document Type: Article
Times cited : (8)

References (18)
  • 1
    • 85087581020 scopus 로고    scopus 로고
    • Structure of a (μ-Oxo)(dihydroxo) diiron(III) complex and Its reactivity toward phosphodiesters
    • Neve, F.; Campagna, A.C. Structure of a (μ-Oxo)(dihydroxo) diiron(III) complex and Its reactivity toward phosphodiesters. Inorg. Chem., 1997, 36, 6150.
    • (1997) Inorg. Chem. , vol.36 , pp. 6150
    • Neve, F.1    Campagna, A.C.2
  • 2
    • 6444234866 scopus 로고    scopus 로고
    • Self-assembled monolayers of Ru/Os dinuclear complexes: Probing monolayer structure and interaction energies by electrochemical means
    • (a) Figgemeier, E.; Constable, E.C.; Housecroft, C.E.; Zimmermann, Y.C. Self-assembled monolayers of Ru/Os dinuclear complexes: probing monolayer structure and interaction energies by electrochemical means. Langmuir, 2004, 20, 9242.
    • (2004) Langmuir , vol.20 , pp. 9242
    • Figgemeier, E.1    Constable, E.C.2    Housecroft, C.E.3    Zimmermann, Y.C.4
  • 3
    • 0001518798 scopus 로고
    • Ruthenium(II) and osmium(II) bis(terpyridine) complexes in covalently-linked multicomponent systems: Synthesis, electrochemical behavior, absorption spectra, and photochemical and photophysical properties
    • (b) Sauvage, J.-P.; Collin, J.-P.; Chambron, J.-C.; Guillerez, S.; Coudret, C.; Balzani, V.; Barigelletti, F.; Cola, L.; Flamigni, L.; Ruthenium(II) and osmium(II) bis(terpyridine) complexes in covalently-linked multicomponent systems: synthesis, electrochemical behavior, absorption spectra, and photochemical and photophysical properties. Chem. Rev., 1994, 94, 993.
    • (1994) Chem. Rev. , vol.94 , pp. 993
    • Sauvage, J.-P.1    Collin, J.-P.2    Chambron, J.-C.3    Guillerez, S.4    Coudret, C.5    Balzani, V.6    Barigelletti, F.7    Cola, L.8    Flamigni, L.9
  • 5
    • 22244433564 scopus 로고
    • The specific synthesis of pyridines and oligopyri- dines
    • Kröhnke, F. The specific synthesis of pyridines and oligopyri- dines. Synthesis, 1976, 1.
    • (1976) Synthesis , pp. 1
    • Kröhnke, F.1
  • 6
    • 11244348930 scopus 로고
    • Ketene dithio acetals as synthetic intermediates. Synthesis of unsaturated 1,5-diketones
    • (a) Potts, K.T.; Cipullo, M.J.; Ralli, P.; Theodoridis, G. Ketene dithio acetals as synthetic intermediates. Synthesis of unsaturated 1,5-diketones. J. Am. Chem. Soc., 1981, 103, 3584.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 3584
    • Potts, K.T.1    Cipullo, M.J.2    Ralli, P.3    Theodoridis, G.4
  • 7
    • 33845553285 scopus 로고
    • Synthesis of 2,6- disubstituted pyridines, polypyridinyls, and annulated pyridines
    • (b) Potts, K.T.; Cipullo, M.J.; Ralliand, P.; Theodoridis, G. Synthesis of 2,6- disubstituted pyridines, polypyridinyls, and annulated pyridines. J. Org. Chem., 1982, 47, 3027.
    • (1982) J. Org. Chem. , vol.47 , pp. 3027
    • Potts, K.T.1    Cipullo, M.J.2    Ralliand, P.3    Theodoridis, G.4
  • 8
    • 0025857450 scopus 로고
    • On the reaction of N- (Diphenylphosphinyl)-l-phenyl ethanimine with aromatic aldehydes giving 4-aryl-2,6-diphenylpyridine derivatives
    • Kobayashi, T.; Kakiuchi, H.; Kato, H. On the reaction of N- (Diphenylphosphinyl)-l-phenyl ethanimine with aromatic aldehydes giving 4-aryl-2,6-diphenylpyridine derivatives. Bull. Chem. Soc. Jpn., 1991, 64, 392.
    • (1991) Bull. Chem. Soc. Jpn. , vol.64 , pp. 392
    • Kobayashi, T.1    Kakiuchi, H.2    Kato, H.3
  • 9
    • 0030600197 scopus 로고    scopus 로고
    • A "one pot" synthesis of polysubstituted pyridines from metallated alkylphosphonates, nitriles and α,β-unsaturated ketones
    • Palacios, F.; Retana, A.M.O.; Oyarzabal, J. A "one pot" synthesis of polysubstituted pyridines from metallated alkylphosphonates, nitriles and α,β-unsaturated ketones. Tetrahedron Lett., 1996, 37, 4577.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 4577
    • Palacios, F.1    Retana, A.M.O.2    Oyarzabal, J.3
  • 10
    • 22244483070 scopus 로고    scopus 로고
    • One-pot synthesis of 2,4,6-triarylpyridines using raw materials under microwave irradiation
    • Tu, S.; Li, T.; Shi, F.; Fang, F.; Zhu, S.; Wei, X.; Zong, Z. One-pot synthesis of 2,4,6-triarylpyridines using raw materials under microwave irradiation. Chem. Lett., 2005, 34, 732.
    • (2005) Chem. Lett. , vol.34 , pp. 732
    • Tu, S.1    Li, T.2    Shi, F.3    Fang, F.4    Zhu, S.5    Wei, X.6    Zong, Z.7
  • 12
    • 14644420299 scopus 로고    scopus 로고
    • Polyethylene glycol and solutions of polyethylene glycol as green reaction media
    • (a)Chen, J.; Spear, S.K.; Huddleston, J.G.; Rogers, R.D. Polyethylene glycol and solutions of polyethylene glycol as green reaction media. Green Chem., 2005, 7, 64;
    • (2005) Green Chem. , vol.7 , pp. 64
    • Chen, J.1    Spear, S.K.2    Huddleston, J.G.3    Rogers, R.D.4
  • 13
    • 58149384265 scopus 로고    scopus 로고
    • A recyclable copper catalysis in modified Friedlander quinoline synthesis
    • (b) Cho, C.S.; Ren, W. X.; Yoon, N.S. A recyclable copper catalysis in modified Friedlander quinoline synthesis. J. Mol. Catal. A: Chem., 2009, 299, 117.
    • (2009) J. Mol. Catal. A: Chem. , vol.299 , pp. 117
    • Cho, C.S.1    Ren, W.X.2    Yoon, N.S.3
  • 14
    • 77951452688 scopus 로고    scopus 로고
    • 4OAc (5 mmol) and PEG-400 (2 mmol) was added to the above mixture at room temperature. Then the mixture was irradiated in microwave (375W) in an open flask for 5-7min. The reaction mixture left to cool to room temperature and added 10ml water, the mixture was filtered and given crude product, the title compound was recrystallized from appropriate solvent to analytical purity
    • 4OAc (5 mmol) and PEG-400 (2 mmol) was added to the above mixture at room temperature. Then the mixture was irradiated in microwave (375W) in an open flask for 5-7min. The reaction mixture left to cool to room temperature and added 10ml water, the mixture was filtered and given crude product, the title compound was recrystallized from appropriate solvent to analytical purity.
  • 16
    • 0002313321 scopus 로고
    • Action du trifluorure de bore sur les aldehydes et les cetones. II.- preparation des fluoborates de triaryl- 2-4-6 pyrylium
    • Lombard, R.; Stephan, J.-P. Action du trifluorure de bore sur les aldehydes et les cetones. II.- preparation des fluoborates de triaryl- 2-4-6 pyrylium. Bull Soc. Chim. Fr. , 1958, 1458.
    • (1958) Bull Soc. Chim. Fr. , pp. 1458
    • Lombard, R.1    Stephan, J.-P.2
  • 17
    • 35448993304 scopus 로고    scopus 로고
    • 2 as a novel and recyclable catalyst for the synthesis of 2,4,6- triarylpyridines under solvent-free conditions
    • 2 as a novel and recyclable catalyst for the synthesis of 2,4,6- triarylpyridines under solvent-free conditions. Catal. Commn., 2007, 8, 1973.
    • (2007) Catal. Commn. , vol.8 , pp. 1973
    • Nagarapu, L.1    Aneesa Peddiraju, R.2    Apuri, S.3
  • 18
    • 67650497402 scopus 로고    scopus 로고
    • Reaction between guanidine hydrochloride and chalcones: An efficient solvent-free synthesis of 2,4,6-triarylpyridines under microwave irradiation
    • Mehdi, A.; Mohammadi, B.; Rahbari, S.; Mirzaei, P. Reaction between guanidine hydrochloride and chalcones: an efficient solvent-free synthesis of 2,4,6-triarylpyridines under microwave irradiation. Chem. Lett., 2008, 37, 1048.
    • (2008) Chem. Lett. , vol.37 , pp. 1048
    • Mehdi, A.1    Mohammadi, B.2    Rahbari, S.3    Mirzaei, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.