메뉴 건너뛰기




Volumn 46, Issue 11, 2010, Pages 1199-1214

Oxidation of organic compounds on NiOOH electrode

Author keywords

NiOOH electrode; organic compounds; oxidation

Indexed keywords

ALIPHATIC ALCOHOL; ALKALINE MEDIUM; AROMATIC ALDEHYDE; BENZYL ALCOHOL; CYCLIC KETONES; ELECTRODE SURFACES; GALVANOSTATIC ELECTROLYSIS; LITERATURE DATA; NIOOH-ELECTRODE; ORGANIC SUBSTRATE; OXIDATION PROCESS; PROCESS EFFICIENCY; RATE OF INTERACTIONS;

EID: 78650612904     PISSN: 10231935     EISSN: 16083342     Source Type: Journal    
DOI: 10.1134/S1023193510110017     Document Type: Article
Times cited : (52)

References (40)
  • 1
    • 33947479742 scopus 로고
    • 1:CAS:528:DyaF38XktFSnsbw%3D 10.1021/jo01052a026
    • K. Nakagawa R. Konaka T. Nakata 1962 J. Org. Chem. 27 5 1597 1:CAS:528:DyaF38XktFSnsbw%3D 10.1021/jo01052a026
    • (1962) J. Org. Chem. , vol.27 , Issue.5 , pp. 1597
    • Nakagawa, K.1    Konaka, R.2    Nakata, T.3
  • 3
    • 33845541006 scopus 로고    scopus 로고
    • An efficient and practical system for the catalytic oxidation of alcohols, aldehydes, and α,β-unsaturated carboxylic acids
    • DOI 10.1021/jo0612574
    • J.M. Grill J.W. Ogle S.A. Miller 2006 J. Org. Chem. 71 25 9291 1:CAS:528:DC%2BD28Xht1Sns7zJ 10.1021/jo0612574 (Pubitemid 44924509)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.25 , pp. 9291-9296
    • Grill, J.M.1    Ogle, J.W.2    Miller, S.A.3
  • 6
    • 0008866449 scopus 로고
    • Ruholl, H. and Schäfer, H.J., Synthesis, 1988, no. 1, p. 54.
    • (1988) Synthesis , vol.1 , pp. 54
    • Ruholl, H.1
  • 17
    • 85081209587 scopus 로고
    • Schneider, R. and Schäfer, H.J., Synthesis, 1989, no. 10, p. 742.
    • (1989) Synthesis , vol.10 , pp. 742
    • Schneider, R.1
  • 23
    • 0001545903 scopus 로고    scopus 로고
    • 1:CAS:528:DyaK2sXnvF2ks7w%3D 10.1016/S0920-5861(97)00049-7
    • A. Kowal S.N. Port R.J. Nichols 1997 Catal. Today 38 4 483 1:CAS:528:DyaK2sXnvF2ks7w%3D 10.1016/S0920-5861(97)00049-7
    • (1997) Catal. Today , vol.38 , Issue.4 , pp. 483
    • Kowal, A.1    Port, S.N.2    Nichols, R.J.3
  • 24
    • 0026077958 scopus 로고
    • 10.1016/S0040-4020(01)87061-7
    • H.J. Schäfer R. Schneider 1991 Tetrahedron 47 s.4-5 715 10.1016/S0040-4020(01)87061-7
    • (1991) Tetrahedron , vol.47 , Issue.4-5 , pp. 715
    • Schäfer, H.J.1    Schneider, R.2
  • 25
    • 1942421771 scopus 로고    scopus 로고
    • 1:CAS:528:DC%2BD2cXjtFGjtrk%3D 10.1016/j.jelechem.2003.11.053
    • P. Parpot S.G. Pires A.P. Bettencourt 2004 J. Electroanal. Chem. 566 2 401 1:CAS:528:DC%2BD2cXjtFGjtrk%3D 10.1016/j.jelechem.2003.11.053
    • (2004) J. Electroanal. Chem. , vol.566 , Issue.2 , pp. 401
    • Parpot, P.1    Pires, S.G.2    Bettencourt, A.P.3
  • 31
  • 36
  • 37
    • 0023453546 scopus 로고
    • 6B 1:CAS:528:DyaL1cXhtVart7k%3D 10.1007/BF01023607
    • J. Hlavaty V. Bakos J. Volke 1987 J. Appl. Electrochem. 17 6b 1228 1:CAS:528:DyaL1cXhtVart7k%3D 10.1007/BF01023607
    • (1987) J. Appl. Electrochem. , vol.17 , pp. 1228
    • Hlavaty, J.1    Bakos, V.2    Volke, J.3
  • 39
    • 0000687750 scopus 로고
    • 1:CAS:528:DyaL3sXksFejtb8%3D 10.1016/0040-4020(82)80110-5
    • J. Kaulen H.J. Schaefer 1982 Tetrahedron 38 3299 1:CAS:528: DyaL3sXksFejtb8%3D 10.1016/0040-4020(82)80110-5
    • (1982) Tetrahedron , vol.38 , pp. 3299
    • Kaulen, J.1    Schaefer, H.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.