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Volumn 14, Issue 11, 2012, Pages 2918-2921

Cine substitution of arenes using the aryl carbamate as a removable directing group

Author keywords

[No Author keywords available]

Indexed keywords

CARBAMIC ACID DERIVATIVE; INDOLE DERIVATIVE; NICKEL;

EID: 84861805391     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol301275u     Document Type: Article
Times cited : (61)

References (58)
  • 15
    • 0035945974 scopus 로고    scopus 로고
    • For a review of cine substitution, see
    • For a review of cine substitution, see: Suwinski, J.; Swierczek, K. Tetrahedron 2001, 57, 1639-1662
    • (2001) Tetrahedron , vol.57 , pp. 1639-1662
    • Suwinski, J.1    Swierczek, K.2
  • 16
    • 0041725326 scopus 로고
    • Nitroarenes can be converted to aryl carboxylic acid derivatives via the von Richter reaction; for a pertinent study, see
    • Nitroarenes can be converted to aryl carboxylic acid derivatives via the von Richter reaction; for a pertinent study, see: Bunnett, J. F. Q. Rev. Chem. Soc. 1958, 12, 1-16
    • (1958) Q. Rev. Chem. Soc. , vol.12 , pp. 1-16
    • Bunnett, J.F.1
  • 38
    • 74949097467 scopus 로고    scopus 로고
    • Aryl pivalate esters can be employed in Pd-catalyzed ortho arylation reactions
    • Aryl pivalate esters can be employed in Pd-catalyzed ortho arylation reactions: Xiao, B.; Fu, Y.; Xu, J.; Gong, T.-J.; Dai, J.-J.; Yi, J.; Liu, L. J. Am. Chem. Soc. 2010, 132, 468-469
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 468-469
    • Xiao, B.1    Fu, Y.2    Xu, J.3    Gong, T.-J.4    Dai, J.-J.5    Yi, J.6    Liu, L.7
  • 53
    • 79952685021 scopus 로고    scopus 로고
    • 2 is commercially available from Strem Chemicals Inc. or Sigma-Aldrich (CAS #19999-87-2). For more information on this catalyst, see: DOI: 10.1002/047084289X.rn01201
    • 2 is commercially available from Strem Chemicals Inc. or Sigma-Aldrich (CAS #19999-87-2). For more information on this catalyst, see: Quasdorf, K. W.; Garg, N. K. Encyclopedia of Reagents for Organic Synthesis 2010, DOI: 10.1002/047084289X.rn01201
    • (2010) Encyclopedia of Reagents for Organic Synthesis
    • Quasdorf, K.W.1    Garg, N.K.2
  • 54
    • 33846064670 scopus 로고    scopus 로고
    • 7 times greater than the acidity of C4-H according to computational studies; see
    • 7 times greater than the acidity of C4-H according to computational studies; see: Shen, K.; Fu, Y.; Li, J.-N.; Liu, L.; Guo, Q.-X. Tetrahedron 2007, 63, 1568-1576
    • (2007) Tetrahedron , vol.63 , pp. 1568-1576
    • Shen, K.1    Fu, Y.2    Li, J.-N.3    Liu, L.4    Guo, Q.-X.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.