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Volumn 6, Issue 4, 2015, Pages 2501-2505

Identifying lead hits in catalyst discovery by screening and deconvoluting complex mixtures of catalyst components

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; FRIEDEL-CRAFTS REACTION; IN SITU PROCESSING; MIXTURES;

EID: 84924943575     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c5sc00268k     Document Type: Article
Times cited : (41)

References (48)
  • 24
    • 84877260239 scopus 로고    scopus 로고
    • For recent reviews on the dehydrative Friedel-Crafts reaction, see
    • E. Dimitrijevic M. S. Taylor ACS Catal. 2013 3 945 962
    • (2013) ACS Catal. , vol.3 , pp. 945-962
    • Dimitrijevic, E.1    Taylor, M.S.2
  • 40
    • 70449519960 scopus 로고    scopus 로고
    • Tri(pentafluorophenyl)boroxine was ruled out as an in situ generated catalyst as it rapidly hydrolysed under the reaction conditions
    • L. F. Li H. S. Lee H. Li X. Q. Yang X. J. Huang Electrochem. Commun. 2009 11 2296 2299
    • (2009) Electrochem. Commun. , vol.11 , pp. 2296-2299
    • Li, L.F.1    Lee, H.S.2    Li, H.3    Yang, X.Q.4    Huang, X.J.5
  • 46
    • 84919621396 scopus 로고    scopus 로고
    • For related Ni-catalyzed alkylation of 8-aminoquinoline benzamides, see
    • A. Yokota Y. Aihara N. Chatani J. Org. Chem. 2014 79 11922 11932
    • (2014) J. Org. Chem. , vol.79 , pp. 11922-11932
    • Yokota, A.1    Aihara, Y.2    Chatani, N.3
  • 48
    • 84893767226 scopus 로고    scopus 로고
    • In the absence of carboxylate ligand only 52% conversion of 9a was observed instead of 75%. In contrast, Chatani and coworkers found that carboxylate ligands suppressed reactivity in substrates possessing a blocking group (see Table 1, entry 13 in ref. 20)
    • X. Wu Y. Zhao H. Ge J. Am. Chem. Soc. 2013 136 1789 1792
    • (2013) J. Am. Chem. Soc. , vol.136 , pp. 1789-1792
    • Wu, X.1    Zhao, Y.2    Ge, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.