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Volumn 12, Issue 12, 2010, Pages 2844-2846

Direct ruthenium-catalyzed C-C coupling of ethanol: Diene hydro-hydroxyethylation to form all-carbon quaternary centers

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; ALKADIENE; RUTHENIUM;

EID: 77953557289     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101077v     Document Type: Article
Times cited : (43)

References (61)
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    • 77953579185 scopus 로고    scopus 로고
    • For selected reviews on sustainable chemical synthesis, see
    • For selected reviews on sustainable chemical synthesis, see
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    • 77953595178 scopus 로고    scopus 로고
    • Renewable Fuels Association (RFA): (accessed March 1, 2010)
    • Renewable Fuels Association (RFA): http://www.ethanolrfa.org/ (accessed March 1, 2010).
  • 7
    • 77953583180 scopus 로고    scopus 로고
    • note
    • Ethanol carbonylation to form propionic acid under the conditions of homogenous catalysis has been described
  • 10
    • 77953589700 scopus 로고    scopus 로고
    • For selected reviews on C-C bond-forming hydrogenation and transfer hydrogenation, see
    • For selected reviews on C-C bond-forming hydrogenation and transfer hydrogenation, see
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    • 77953555914 scopus 로고    scopus 로고
    • For isolated examples of stereoselective carbonyl allylboration to furnish syn- configured neopentyl homoallylic alcohols, see
    • For isolated examples of stereoselective carbonyl allylboration to furnish syn- configured neopentyl homoallylic alcohols, see
  • 16
    • 77953558173 scopus 로고    scopus 로고
    • For methanol dehydrogenation, DH = +84 kJ/mol. For ethanol dehydrogenation, DH = +68 kJ/mol
    • For methanol dehydrogenation, DH = +84 kJ/mol. For ethanol dehydrogenation, DH = +68 kJ/mol
  • 19
    • 43949117421 scopus 로고    scopus 로고
    • For ruthenium catalyzed C-C bond-forming transfer hydrogenation developed in our laboratory, see the following. Dienes
    • For ruthenium catalyzed C-C bond-forming transfer hydrogenation developed in our laboratory, see the following. Dienes: Shibahara, F.; Bower, J. F.; Krische, M. J. J. Am. Chem. Soc. 2008, 130, 6338
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 6338
    • Shibahara, F.1    Bower, J.F.2    Krische, M.J.3
  • 25
  • 29
    • 77953546290 scopus 로고    scopus 로고
    • For related catalytic C-C couplings that occur by way of nucleophilic ruthenium p -allyls, see
    • For related catalytic C-C couplings that occur by way of nucleophilic ruthenium p -allyls, see
  • 35
    • 77953605914 scopus 로고    scopus 로고
    • For selected reviews of ruthenium-catalyzed C-C coupling beyond olefin metathesis, see
    • For selected reviews of ruthenium-catalyzed C-C coupling beyond olefin metathesis, see
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    • 77953556901 scopus 로고    scopus 로고
    • For catalytic intermolecular diene-aldehyde reductive coupling, see
    • For catalytic intermolecular diene-aldehyde reductive coupling, see
  • 52
    • 77953562317 scopus 로고    scopus 로고
    • For a recent review encompassing nickel-catalyzed diene-aldehyde reductive coupling, see
    • For a recent review encompassing nickel-catalyzed diene-aldehyde reductive coupling, see
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    • 77953557545 scopus 로고    scopus 로고
    • note
    • 15, and dppb
  • 57
    • 77953603410 scopus 로고    scopus 로고
    • For isomerization of ruthenium p -allyls, see
    • For isomerization of ruthenium p -allyls, see
  • 59
    • 77953583179 scopus 로고    scopus 로고
    • For related amine-mediated "hydro-aminoalkylation" of α-olefins, see
    • For related amine-mediated "hydro-aminoalkylation" of α-olefins, see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.