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Volumn 67, Issue 49, 2011, Pages 9565-9575

Copper catalyzed/mediated synthetic methodology for ebselen and related isoselenazolones

Author keywords

[No Author keywords available]

Indexed keywords

1,10 PHENANTHROLINE; 2 (2 BROMOPHENYL)BENZO[1,2]SELENAZOL 3(2H) ONE; 2 (2 CHLOROPHENYL)BENZO[1,2]SELENAZOL 3(2H) ONE; 2 (2 FLUOROPHENYL)BENZO[1,2]SELENAZOL 3(2H) ONE; 2 (2 METHOXYPHENYL)BENZO[1,2]SELENAZOL 3(2H) ONE; 2 BENZYL 5 (METHYLTHIO)BENZO[1,2]SELENAZOL 3(2H) ONE; 2 BENZYL 5 METHOXYBENZO[1,2]SELENAZOL 3(2H) ONE; 2 BENZYL 7 METHOXYBENZO[1,2]SELENAZOL 3(2H) ONE; 2 BENZYL [1,2] SELENAZOLO [5,4 BETA]PYRIDIN 3(2H) ONE; 2 BENZYLBENZO[1,2]SELENAZOL 3(2H) ONE; 2 BROMO ARYLAMIDE; 2 BUTYL [1,2] SELENAZOLO [5,4 BETA]PYRIDIN 3(2H) ONE; 2 CHLORO 3 METHOXY N PHENYLBENZAMIDE; 2 CHLORO ARYLAMIDE; 2 CYCLOHEXYL [1,2] SELENAZOLO [5,4 BETA]PYRIDIN 3(2H) ONE; 2 IODO ARYLAMIDE; 2 IODO N (2 CHLOROPHENYL)BENZAMIDE; 6,7 DIMETHOXY 2 PHENYLBENZO[1,2]SELENAZOL 3(2H) ONE; 7 METHOXY 2 PHENYLBENZO[1,2]SELENAZOL 3(2H) ONE; AMIDE; COPPER; DIARYLDISELENIDE DERIVATIVE; EBSELEN; METHOXYAMINE; NITROGEN; ORGANOSELENIUM DERIVATIVE; POTASSIUM CARBONATE; SELENAZOLE DERIVATIVE; SELENIUM; SUCCINIMIDE; UNCLASSIFIED DRUG;

EID: 80555150533     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.09.141     Document Type: Article
Times cited : (66)

References (78)
  • 1
    • 0035385139 scopus 로고    scopus 로고
    • references therein
    • For antioxidant activities of isoselenazolones see: G. Mugesh, W.-W. du Mont, and H. Sies Chem. Rev. 101 2001 2125 and references therein
    • (2001) Chem. Rev. , vol.101 , pp. 2125
    • Mugesh, G.1    Du Mont, W.-W.2    Sies, H.3
  • 11
    • 78649287952 scopus 로고    scopus 로고
    • see recent references on Se-N heterocycles
    • K.P. Bhabak, and G. Mugesh Acc. Chem. Res. 43 2010 1408 see recent references on Se-N heterocycles
    • (2010) Acc. Chem. Res. , vol.43 , pp. 1408
    • Bhabak, K.P.1    Mugesh, G.2
  • 20
    • 84906701803 scopus 로고
    • Chem. Abstr. 96 1982 199699v
    • (1982) Chem. Abstr. , vol.96
  • 42
    • 80555145431 scopus 로고    scopus 로고
    • Selenium/Sulfur Coupling Reactions
    • Selenium/Sulfur Coupling Reactions
  • 53
    • 39649090309 scopus 로고    scopus 로고
    • For theoretical study on methoxy substituted ebselen, see
    • For theoretical study on methoxy substituted ebselen, see: J.K. Pearson, and R.J. Boyd J. Phys. Chem. A 112 2008 1013
    • (2008) J. Phys. Chem. A , vol.112 , pp. 1013
    • Pearson, J.K.1    Boyd, R.J.2
  • 54
    • 53849112342 scopus 로고    scopus 로고
    • For methoxy substituted GPx mimics, see
    • For methoxy substituted GPx mimics, see: K.P. Bhabak, and G. Mugesh Chem. - Eur. J. 14 2008 8640
    • (2008) Chem. - Eur. J. , vol.14 , pp. 8640
    • Bhabak, K.P.1    Mugesh, G.2
  • 67
    • 80555145433 scopus 로고
    • Ger. Offen. Patent: DE2012216
    • Merger, F. Ger. Offen. Patent: DE2012216, 1971
    • (1971)
    • Merger, F.1
  • 68
    • 84918025929 scopus 로고
    • Chem. Abstr. 76 1972 3683e
    • (1972) Chem. Abstr. , vol.76
  • 69
    • 80555131330 scopus 로고
    • Patent: CH546759 DE2048080
    • Merger, F. Patent: CH546759 DE2048080, 1971
    • (1971)
    • Merger, F.1
  • 70
    • 80555145429 scopus 로고    scopus 로고
    • Chem. Abstr. 77, p 61977.
    • Chem. Abstr. , vol.77 , pp. 61977
  • 71
    • 80555138412 scopus 로고
    • COLLECT. VOL. VI Organic Syntheses, Inc. ()
    • H.J. Reich, M.L. Cohen, and P.D. Clark Org. Synth Collect. Vol. VI, 533 1988 Organic Syntheses, Inc. (http://www.orgsyn.org/orgsyn/prep.asp?prep= cv6p0533)
    • (1988) Org. Synth , vol.533
    • Reich, H.J.1    Cohen, M.L.2    Clark, P.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.