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Volumn 67, Issue 19, 2011, Pages 3360-3362

Electron-transfer-induced reductive cleavage of chlorinated aryloxyalkanoic acids

Author keywords

Aryloxyalkanoic acid; Chlorinated herbicide; Electron transfer; Hydrodealkylation; Hydrodehalogenation; Reduction

Indexed keywords

2,4 DICHLOROPHENOXYACETIC ACID; ALKANOIC ACID; HERBICIDE; LITHIUM DERIVATIVE; METAL; SODIUM;

EID: 79954990299     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2011.03.057     Document Type: Article
Times cited : (12)

References (36)
  • 1
    • 79955039947 scopus 로고    scopus 로고
    • Acronyms of aryloxyalkanoic acid are taken from the Compendium of Pesticide Common Names
    • Acronyms of aryloxyalkanoic acid are taken from the Compendium of Pesticide Common Names, http://www.alanwood.net/pesticides/class-herbicides. html.
  • 2
    • 0004192571 scopus 로고
    • Committee to Review the Health Effects in Vietnam Veterans on Exposure to Herbicides, Division of Health Promotion and Disease Prevention, Institute of Medicine Veterans and Agent Orange National Academic Washington, D.C.
    • Committee to Review the Health Effects in Vietnam Veterans on Exposure to Herbicides, Division of Health Promotion and Disease Prevention, Institute of Medicine Veterans and Agent Orange 1994 National Academic Washington, D.C. pp 74-110
    • (1994) Veterans and Agent Orange
  • 10
    • 79954989045 scopus 로고    scopus 로고
    • for selected procedures, see
    • for selected procedures, see:
  • 22
    • 79954997254 scopus 로고    scopus 로고
    • We did not observe evidences of competitive dealkoxylation reactions (aromatic C-O bond cleavage, see Ref. 10)
    • We did not observe evidences of competitive dealkoxylation reactions (aromatic C-O bond cleavage, see Ref. 10 ).
  • 23
    • 79954994482 scopus 로고    scopus 로고
    • The reductive cleavage of an aromatic carbon-halogen bond is usually considered to proceed via the intermediate formation of an aromatic radical, which can be further reduced to the corresponding carbanion. See Ref. 8 and references therein
    • The reductive cleavage of an aromatic carbon-halogen bond is usually considered to proceed via the intermediate formation of an aromatic radical, which can be further reduced to the corresponding carbanion. See Ref. 8 and references therein.
  • 27
    • 79955038055 scopus 로고
    • Chem. Abstr. 57 1962 5852c
    • (1962) Chem. Abstr. , vol.57
  • 36
    • 79955048566 scopus 로고    scopus 로고
    • ®
    • ®.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.