메뉴 건너뛰기




Volumn 38, Issue 11, 2008, Pages 1745-1752

Zeolite H-Y-supported copper(II) nitrate: A simple and effective solid-supported reagent for nitration of phenols and their derivatives

Author keywords

Microwave; Nitration; Phenol; Supported reagent; Zeolite

Indexed keywords

CUPRIC ION; NITRATE; PHENOL DERIVATIVE; ZEOLITE;

EID: 45749085793     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910801982456     Document Type: Article
Times cited : (20)

References (17)
  • 2
    • 0003970635 scopus 로고
    • Cambridge University Press: Cambridge
    • (b) Schofield, K. Aromatic Nitration; Cambridge University Press: Cambridge, 1980.
    • (1980) Aromatic Nitration
    • Schofield, K.1
  • 3
    • 0033615743 scopus 로고    scopus 로고
    • Organic transformations using zeolites and zeotype materials
    • Sen, S. E.; Smith, S. M.; Sullivan, K. A. Organic transformations using zeolites and zeotype materials. Tetrahedron 1999, 55, 12657-12698.
    • (1999) Tetrahedron , vol.55 , pp. 12657-12698
    • Sen, S.E.1    Smith, S.M.2    Sullivan, K.A.3
  • 4
    • 0037043213 scopus 로고    scopus 로고
    • Zeolite-mediated regioselective nitration of phenol in solid state
    • Esakkidurai, T.; Pitchumani, K. Zeolite-mediated regioselective nitration of phenol in solid state. J. Mol. Catal. A: Chem. 2002, 185, 305-309.
    • (2002) J. Mol. Catal. A: Chem , vol.185 , pp. 305-309
    • Esakkidurai, T.1    Pitchumani, K.2
  • 5
    • 0036847207 scopus 로고    scopus 로고
    • Development of a system for clean and regioselective mononitration of aromatic compounds involving a microporous solid, dinitrogen tetroxide and air
    • Smith, K.; Almeer, S.; Black, S. J.; Peters, C. Development of a system for clean and regioselective mononitration of aromatic compounds involving a microporous solid, dinitrogen tetroxide and air. J. Mater. Chem. 2002, 12, 3285-3289.
    • (2002) J. Mater. Chem , vol.12 , pp. 3285-3289
    • Smith, K.1    Almeer, S.2    Black, S.J.3    Peters, C.4
  • 6
    • 0032515129 scopus 로고    scopus 로고
    • Smith, K.; Musson, A.; DeBoos, G. A. A novel method for the nitration of simple aromatic compounds. J. Org. Chem. 1998, 63, 8448-8454;
    • (a) Smith, K.; Musson, A.; DeBoos, G. A. A novel method for the nitration of simple aromatic compounds. J. Org. Chem. 1998, 63, 8448-8454;
  • 7
    • 0035948276 scopus 로고    scopus 로고
    • Zeolite-assisted nitration of neat tolune and chlorobenzene wiht a nitrogen dioxide/molecular oxygen system. Remarkable enhancement of paraselectivity
    • (b) Peng, X.; Suzuki, H.; Lu, C. Zeolite-assisted nitration of neat tolune and chlorobenzene wiht a nitrogen dioxide/molecular oxygen system. Remarkable enhancement of paraselectivity. Tetrahedron Lett. 2001, 42, 4357-4359.
    • (2001) Tetrahedron Lett , vol.42 , pp. 4357-4359
    • Peng, X.1    Suzuki, H.2    Lu, C.3
  • 9
    • 0034649133 scopus 로고    scopus 로고
    • Surface-mediated highly efficient regioselective nitration of aromatic compounds by bismuth nitrate
    • Samajdar, S.; Becker, F. F.; Banik, B. K. Surface-mediated highly efficient regioselective nitration of aromatic compounds by bismuth nitrate. Tetrahedron Lett. 2000, 41, 8017.
    • (2000) Tetrahedron Lett , vol.41 , pp. 8017
    • Samajdar, S.1    Becker, F.F.2    Banik, B.K.3
  • 10
    • 0001755150 scopus 로고    scopus 로고
    • Gigante, B.; Prazeres, A. O.; Marcelo-Curto, M. J.; Cornelis, A.; Laszlo, P. Mild and selective nitration by claycop. J. Org. Chem. 1995, 60, 3445-3447.
    • Gigante, B.; Prazeres, A. O.; Marcelo-Curto, M. J.; Cornelis, A.; Laszlo, P. Mild and selective nitration by "claycop." J. Org. Chem. 1995, 60, 3445-3447.
  • 11
    • 33646793643 scopus 로고    scopus 로고
    • Silica-gel-supported ceric ammonium nitrate (CAN): A simple and efficient solid-supported reagent for oxidation of oxygenated aromatic compounds to quinones
    • Ali, M. H.; Niedbalski, M.; Bohnert, G.; Bryant, D. Silica-gel-supported ceric ammonium nitrate (CAN): A simple and efficient solid-supported reagent for oxidation of oxygenated aromatic compounds to quinones. Synth. Commun. 2006, 36, 1751-1759.
    • (2006) Synth. Commun , vol.36 , pp. 1751-1759
    • Ali, M.H.1    Niedbalski, M.2    Bohnert, G.3    Bryant, D.4
  • 12
    • 0036643965 scopus 로고    scopus 로고
    • Counterion effects in indium-catalysed aromatic electrophilic substitution reactions
    • Frost, C. G.; Hartley, J. P.; Griffin, D. Counterion effects in indium-catalysed aromatic electrophilic substitution reactions. Tetrahedron Lett. 2002, 43, 4789-4791.
    • (2002) Tetrahedron Lett , vol.43 , pp. 4789-4791
    • Frost, C.G.1    Hartley, J.P.2    Griffin, D.3
  • 13
    • 1642343738 scopus 로고    scopus 로고
    • Lanthanide(III) nosylates as new nitration catalysts
    • Parac-Vogt, T. N.; Binnemans, K. Lanthanide(III) nosylates as new nitration catalysts. Tetrahedron Lett. 2004, 45, 3137-3139.
    • (2004) Tetrahedron Lett , vol.45 , pp. 3137-3139
    • Parac-Vogt, T.N.1    Binnemans, K.2
  • 14
    • 33947093286 scopus 로고
    • Aromatic substitution- perfluorinated resinsulfonic acid catalyzed nitration of aromatics
    • Olah, G. A.; Malhotra, R.; Narang, S. C. Aromatic substitution- perfluorinated resinsulfonic acid catalyzed nitration of aromatics. J. Org. Chem. 1978, 43, 4628.
    • (1978) J. Org. Chem , vol.43 , pp. 4628
    • Olah, G.A.1    Malhotra, R.2    Narang, S.C.3
  • 15
    • 0001639432 scopus 로고
    • Onium Ions - Ambident Reactivity of the nitronium ion: Nitration vs. oxidation of heteroorganic (S, Se, P, As, Sb) compounds: Preparation and NMR spectroscopic (13C, 15 N, 31P) study of nitro and nitrito onium ions
    • Chem. Soc
    • Olah, G. A.; Gupta, B. G. B.; Narang, S. C. Onium Ions - Ambident Reactivity of the nitronium ion: Nitration vs. oxidation of heteroorganic (S, Se, P, As, Sb) compounds: Preparation and NMR spectroscopic (13C, 15 N, 31P) study of nitro and nitrito onium ions. J. Am. Chem. Soc. 1979, 101, 5317.
    • (1979) J. Am , vol.101 , pp. 5317
    • Olah, G.A.1    Gupta, B.G.B.2    Narang, S.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.