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Volumn 45, Issue 1, 2004, Pages 17-19

Bis(pentafluorophenyl) disulfide as a hydrogen abstractor and an electron acceptor from the resulting radical intermediate

Author keywords

Electron transfer; H abstraction; Pentafluorobenzenethiyl radical; Thiyl radical

Indexed keywords

ALCOHOL DERIVATIVE; BENZOIC ACID DERIVATIVE; BIS(PENTAFLUOROPHENYL)DISULFIDE; CARBENE; DIOXANE DERIVATIVE; DISULFIDE; ETHER DERIVATIVE; HYDROGEN; RADICAL; UNCLASSIFIED DRUG;

EID: 0742322138     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.10.211     Document Type: Article
Times cited : (5)

References (15)
  • 2
    • 0002103490 scopus 로고
    • Sulfur-Centered Reaction Intermediates in Chemistry and Biology C. Chatgilialoglu, Asmus K.-D.
    • New York and London: Plenum
    • Schoneich C., Bonifacic M., Dillinger U., Asmus K.-D. Sulfur-Centered Reaction Intermediates in Chemistry and Biology. Chatgilialoglu C., Asmus K.-D. NATO ASI Series A. Vol. 197:1990;367-376 Plenum, New York and London.
    • (1990) NATO ASI Series a , vol.197 , pp. 367-376
    • Schoneich, C.1    Bonifacic, M.2    Dillinger, U.3    Asmus, K.-D.4
  • 3
    • 0004081209 scopus 로고    scopus 로고
    • Z.B. Alfassi. Chichester: John-Wiley & Sons
    • Wardman P. Alfassi Z.B. S-centered Radicals. 1999;289-309 John-Wiley & Sons, Chichester.
    • (1999) S-centered Radicals , pp. 289-309
    • Wardman, P.1
  • 9
    • 85030913909 scopus 로고    scopus 로고
    • note
    • 2) and GPC (gel permeation chromatography) on JAIGEL-1H eluted by 1,2-dichloroethne.
  • 10
    • 85030892089 scopus 로고    scopus 로고
    • note
    • 1H NMR (400 MHz) δ -0.08 (3H, s), -0.04 (3H, s), 0.84 (9H, s), 6.17 (1H, s), 7.26-7.31 (3H, m), 7.34-7.36 (2H, m).
  • 12
    • 85030905830 scopus 로고    scopus 로고
    • note
    • 1H NMR (400 MHz) 1.32 (6H, s), 1.96 (2H, t, J=6.8 ), 4.25 (2H, t, J=6.8 ), 7.44 (2H, t, J=7.5 ), 7.55 (1H, t, J=7.5 ), 8.04 (2H, d, J=7.5 ).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.