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Volumn 28, Issue 17, 2009, Pages 5112-5121

Chelating NHC ruthenium(II) complexes as robust homogeneous hydrogenation catalysts

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLATE GROUPS; CHELATING GROUPS; DONOR GROUPS; E-OLEFIN; ELECTROCHEMICAL ANALYSIS; ELECTRONIC IMPACT; FUNCTIONALIZED; HIGH-PRESSURE NMR; HYDROGENATION CATALYST; IN-SITU; METAL CENTERS; N-HETEROCYCLIC CARBENE LIGANDS; NMR SPECTROSCOPY; REDUCING CONDITIONS; REDUCTIVE ELIMINATION; RUTHENIUM COMPLEXES; THIOETHERS;

EID: 69949134471     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om900356w     Document Type: Article
Times cited : (128)

References (107)
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    • 3 groups show the largest differences, whereas most other protons overlap significantly. Hence we assume the presence of two diastereoisomers that are characterized by the specific orientation of the olefin, which may coordinate either parallel or orthogonal to the Cp plane
    • 3 groups show the largest differences, whereas most other protons overlap significantly. Hence we assume the presence of two diastereoisomers that are characterized by the specific orientation of the olefin, which may coordinate either parallel or orthogonal to the Cp plane
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    • 2
    • 2.
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    • P 49.8)
    • P 49.8).
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    • 6-acetone) was attributed to the formation of the imidazolium salt. These shifts compare well with those of an authentic sample of N-methyl-N'-propylimidazolium comprising a bromide anion
    • 6-acetone) was attributed to the formation of the imidazolium salt. These shifts compare well with those of an authentic sample of N-methyl-N'-propylimidazolium comprising a bromide anion.
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    • See the Supporting Information for further details
    • See the Supporting Information for further details.
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    • The high-field part of the AX signal was covered by solvent resonances
    • The high-field part of the AX signal was covered by solvent resonances.
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    • +/Fc) couple
    • +/Fc) couple.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.