메뉴 건너뛰기




Volumn 16, Issue 5, 2011, Pages 3563-3568

Reduction of nitroarenes to azoxybenzenes by potassium borohydride in water

Author keywords

Azoxybenzenes; Nitroarenes; PEG 400; Potassium borohydride; Water

Indexed keywords

AMFENAC; AZO COMPOUND; BORANE DERIVATIVE; MACROGOL DERIVATIVE; NITRO DERIVATIVE; POTASSIUM BOROHYDRIDE; WATER;

EID: 79957615176     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules16053563     Document Type: Article
Times cited : (22)

References (17)
  • 1
    • 33947461962 scopus 로고
    • The reduction of nitrobenzene to azoxybenzene by sodium borohydride
    • Weill, C.E.; Panson, G.S. The reduction of nitrobenzene to azoxybenzene by sodium borohydride. J. Org. Chem. 1956, 21, 803.
    • (1956) J. Org. Chem , vol.21 , pp. 803
    • Weill, C.E.1    Panson, G.S.2
  • 2
    • 0000030397 scopus 로고
    • Reduction of aromatic nitro compounds with sodium borohydride in dimethyl sulfoxide or sulfolane. Synthesis of azo or azoxy derivatives
    • Hutchins, R.O.; Lamson, D.W.; Rua, L.; Milewski, C.; Maryanoff, B. Reduction of aromatic nitro compounds with sodium borohydride in dimethyl sulfoxide or sulfolane. Synthesis of azo or azoxy derivatives. J. Org. Chem. 1971, 36, 803-806.
    • (1971) J. Org. Chem , vol.36 , pp. 803-806
    • Hutchins, R.O.1    Lamson, D.W.2    Rua, L.3    Milewski, C.4    Maryanoff, B.5
  • 3
    • 0000864980 scopus 로고
    • The reduction of aromatic nitro compounds by potassium borohydride
    • Shine, H.J.; Mallory, H.E. The reduction of aromatic nitro compounds by potassium borohydride. J. Org. Chem. 1962, 27, 2390-2391.
    • (1962) J. Org. Chem , vol.27 , pp. 2390-2391
    • Shine, H.J.1    Mallory, H.E.2
  • 5
    • 0029785695 scopus 로고    scopus 로고
    • Catalytic reduction of nitroarenes to azoxybenzenes with sodium borohydride in the presence of bismuth
    • Ren, P.D.; Pan, S.F.; Dong, T.W.; Wu, S.H. Catalytic reduction of nitroarenes to azoxybenzenes with sodium borohydride in the presence of bismuth. Synth. Commun. 1996, 26, 3903-3908.
    • (1996) Synth. Commun , vol.26 , pp. 3903-3908
    • Ren, P.D.1    Pan, S.F.2    Dong, T.W.3    Wu, S.H.4
  • 6
    • 0346250079 scopus 로고    scopus 로고
    • Selective Reduction of an Aromatic Nitro Group to an Azoxy Unit in the Presence of an Aliphatic Nitro Group
    • DOI 10.1007/s00706-002-0549-9
    • Siemeling, U.; Türk, T.; Vorfeld, U.; Fink, H. Selective reduction of an aromatic nitro group to an azoxy Unit in the presence of an aliphatic nitro group. Monatsh. Chem. 2003, 134, 419-423. (Pubitemid 38019435)
    • (2003) Monatshefte fur Chemie , vol.134 , Issue.3 , pp. 419-423
    • Siemeling, U.1    Turk, T.2    Vorfeld, U.3    Fink, H.4
  • 7
    • 0001051714 scopus 로고
    • Sodium arenetellurolate-catalyzed selective conversion of nitro aromatics to aromatic azoxy or azo compounds and its application for facile preparation of 3,3'- and 4,4'-bis[.beta.-(aryltelluro)vinyl] azobenzenes from (3- and 4-nitrophenyl)acetylenes
    • Ohe, K.; Uemura, S.; Sugita, N.; Masuda, H.; Taga, T. Sodium arenetellurolate-catalyzed selective conversion of nitro aromatics to aromatic azoxy or azo compounds and its application for facile preparation of 3,3'- and 4,4'-bis[.beta.-(aryltelluro)vinyl] azobenzenes from (3- and 4-nitrophenyl)acetylenes. J. Org. Chem. 1989, 54, 4169-4174.
    • (1989) J. Org. Chem , vol.54 , pp. 4169-4174
    • Ohe, K.1    Uemura, S.2    Sugita, N.3    Masuda, H.4    Taga, T.5
  • 8
    • 0003041078 scopus 로고
    • Linear unsubstituted polyethylene glycols as phase transfer catalysts
    • Balasubramanian, D.; Sukumar, P.; Chandani, B. Linear unsubstituted polyethylene glycols as phase transfer catalysts. Tetrahedron Lett. 1979, 20, 3543-3544.
    • (1979) Tetrahedron Lett , vol.20 , pp. 3543-3544
    • Balasubramanian, D.1    Sukumar, P.2    Chandani, B.3
  • 9
    • 0242712519 scopus 로고
    • Catalytic activity of polyethylene glycols in the reduction of carbonyl compounds under phase-transfer catalyzed conditions
    • Zupancic, B.G.; Kokalj, M. Catalytic activity of polyethylene glycols in the reduction of carbonyl compounds under phase-transfer catalyzed conditions. Synth. Commun. 1982, 12, 881-886.
    • (1982) Synth. Commun , vol.12 , pp. 881-886
    • Zupancic, B.G.1    Kokalj, M.2
  • 10
    • 22844438263 scopus 로고
    • Mechanism of base-catalyzed reactions in phase-transfer systems with poly(ethy1ene glycols) as catalysts. The isomerization of allylanisole
    • and references cited therein
    • Neumann, R.; Sasson, Y. Mechanism of base-catalyzed reactions in phase-transfer systems with poly(ethy1ene glycols) as catalysts. The isomerization of allylanisole. J. Org. Chem. 1984, 49, 3448-3451, and references cited therein.
    • (1984) J. Org. Chem , vol.49 , pp. 3448-3451
    • Neumann, R.1    Sasson, Y.2
  • 11
    • 0242459935 scopus 로고    scopus 로고
    • First Examples of Transition-Metal Free Sonogashira-Type Couplings
    • DOI 10.1021/ol035485l
    • Leadbeater, N.E.; Marco, M.; Tominack, B.J. First examples of transition-metal free Sonogashiratype couplings. Org. Lett. 2003, 5, 3919-3922. (Pubitemid 37412166)
    • (2003) Organic Letters , vol.5 , Issue.21 , pp. 3919-3922
    • Leadbeater, N.E.1    Marco, M.2    Tominack, B.J.3
  • 12
    • 65949089856 scopus 로고    scopus 로고
    • Microwave-irradiated synthesis of nitrophen using PEG 400 as phase transfer catalyst and solvent
    • and references cited therein
    • Yadav, G.D.; Motirale, B.G. Microwave-irradiated synthesis of nitrophen using PEG 400 as phase transfer catalyst and solvent. Org. Proc. Res. Devel. 2009, 13, 341-348, and references cited therein.
    • (2009) Org. Proc. Res. Devel , vol.13 , pp. 341-348
    • Yadav, G.D.1    Motirale, B.G.2
  • 13
    • 11744313735 scopus 로고
    • New phase transfer catalyzing reagents-polyethylene glycol and its derivatives
    • Huang, X.; Huang, Z.Z. New phase transfer catalyzing reagents- polyethylene glycol and its derivatives. Huaxue Shiji 1985, 7, 20-22.
    • (1985) Huaxue Shiji , vol.7 , pp. 20-22
    • Huang, X.1    Huang, Z.Z.2
  • 14
    • 0037012915 scopus 로고    scopus 로고
    • Wittig-type olefination catalyzed by PEG-telluride
    • DOI 10.1021/jo025586h
    • Huang, Z.Z.; Ye, S.; Xia, W.; Yu, Y.H.; Tang, Y. Wittig-type olefination catalyzed by PEG-telluride. J. Org. Chem. 2002, 67, 3096-3103. (Pubitemid 34457270)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.9 , pp. 3096-3103
    • Huang, Z.-Z.1    Ye, S.2    Xia, W.3    Yu, Y.-H.4    Tang, Y.5
  • 15
    • 33947297060 scopus 로고
    • Thallium in organic synthesis. XI. Preparation of azoxy compounds
    • Mckillop, A.; Raphael, R.A.; Taylor, E.C. Thallium in organic synthesis. XI. Preparation of azoxy compounds. J. Org. Chem. 1970, 35, 1670-1672.
    • (1970) J. Org. Chem , vol.35 , pp. 1670-1672
    • Mckillop, A.1    Raphael, R.A.2    Taylor, E.C.3
  • 16
    • 0001468915 scopus 로고
    • Lanthanides in organic synthesis. Samarium metal promoted selective formation of azoxy compounds
    • Hou, Z.M.; Fujiwara, Y.; Taniguchi, H. Lanthanides in organic synthesis. Samarium metal promoted selective formation of azoxy compounds. J. Org. Chem. 1988, 53, 3118-3120.
    • (1988) J. Org. Chem , vol.53 , pp. 3118-3120
    • Hou, Z.M.1    Fujiwara, Y.2    Taniguchi, H.3
  • 17
    • 0001238482 scopus 로고
    • The absorption spectra of aromatic azo and related compounds. I. azoxybenzenes
    • Gore, P.H., Wheeler, O.H. The absorption spectra of aromatic azo and related compounds. I. azoxybenzenes. J. Am. Chem. Soc. 1956, 78, 2160-2163.
    • (1956) J. Am. Chem. Soc , vol.78 , pp. 2160-2163
    • Gore, P.H.1    Wheeler, O.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.