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Volumn 8, Issue 5, 2017, Pages 3618-3622

Mild, visible light-mediated decarboxylation of aryl carboxylic acids to access aryl radicals

Author keywords

[No Author keywords available]

Indexed keywords

ATOMS; CARBOXYLATION; CARBOXYLIC ACIDS;

EID: 85020434015     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c6sc05533h     Document Type: Article
Times cited : (136)

References (68)
  • 4
    • 85021673611 scopus 로고    scopus 로고
    • For recent reviews on the visible light-promoted decarboxylation of alkyl carboxylic acids see
    • For recent reviews on the visible light-promoted decarboxylation of alkyl carboxylic acids see
  • 7
    • 85021690830 scopus 로고    scopus 로고
    • references therein. For recent publications see
    • and references therein. For recent publications see
  • 12
    • 85021633668 scopus 로고    scopus 로고
    • For selected reviews on visible light photoredox catalysis, see
    • For selected reviews on visible light photoredox catalysis, see
  • 38
    • 85021645429 scopus 로고    scopus 로고
    • -1)
    • -1)
  • 39
    • 85021673566 scopus 로고    scopus 로고
    • 4)
    • 4)
  • 43
    • 85021671202 scopus 로고    scopus 로고
    • For selected example of HAT with, see
    • For selected example of HAT with I, see
    • , vol.1
  • 57
    • 0001478826 scopus 로고
    • The Hunsdiecker and Related Reactions
    • in, ed., Pergamon Press, Oxford
    • The Hunsdiecker and Related Reactions, in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, vol. 7, Pergamon Press, Oxford, 1991, p.717
    • (1991) Comprehensive Organic Synthesis , vol.7 , pp. 717
    • Trost, B.M.1    Fleming, I.2
  • 58
    • 85021643846 scopus 로고    scopus 로고
    • 2) in chlorobenzene results in the formation of a mixture of biaryl, benzoate ester and benzoic acid products. Similar reactions, but with benzoyl hypobromites, affords only benzoate ester products, see
    • 2) in chlorobenzene results in the formation of a mixture of biaryl, benzoate ester and benzoic acid products. Similar reactions, but with benzoyl hypobromites, affords only benzoate ester products, see
    • In Situ
  • 60
    • 85021629617 scopus 로고    scopus 로고
    • See ESI for details of the synthesis and characterisation of
    • See ESI for details of the synthesis and characterisation of 1
    • , vol.1
  • 61
    • 85021639771 scopus 로고    scopus 로고
    • 2 (3.5 equiv.)) afforded phenyl 2-chlorobenzoate (12%). No chlorinated arene by-products were formed, only bromobenzene mixtures
    • 2 (3.5 equiv.)) afforded phenyl 2-chlorobenzoate (12%). No chlorinated arene by-products were formed, only bromobenzene mixtures
  • 63
    • 85021625941 scopus 로고    scopus 로고
    • 4), ref. 8 a
    • 4), ref. 8 a


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.