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Volumn 133, Issue 34, 2011, Pages 13634-13645

Pyranoside phosphite-oxazoline ligands for the highly versatile and enantioselective Ir-catalyzed hydrogenation of minimally functionalized olefins. A combined theoretical and experimental study

Author keywords

[No Author keywords available]

Indexed keywords

COMPUTATIONAL PREDICTIONS; DFT STUDY; ENANTIOSELECTIVE; EXPERIMENTAL STUDIES; FUNCTIONALIZED; FUNCTIONALIZED SUBSTRATES; SIZE DIFFERENCE;

EID: 80052098490     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja204948k     Document Type: Article
Times cited : (153)

References (96)
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    • Jacobsen, E. N. Pfaltz, A. Yamamoto, H. Springer-Verlag: Berlin
    • Brown, J. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Berlin, 1999; Vol. I, pp 121-182.
    • (1999) Comprehensive Asymmetric Catalysis , vol.1 , pp. 121-182
    • Brown, J.M.1
  • 61
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    • A special issue has been devoted to "fluorine in the Life Sciences"
    • A special issue has been devoted to "Fluorine in the Life Sciences". ChemBioChem 2004, 5, 559.
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  • 88
    • 79955591931 scopus 로고    scopus 로고
    • Recently, the group of Hopmann et al. has performed a computationally study using a phosphine-oxazoline (PHOX)-based iridium catalyst, which indicates that the hydrogenation of S1 follows the 3/5-Meta pathway
    • Recently, the group of Hopmann et al. has performed a computationally study using a phosphine-oxazoline (PHOX)-based iridium catalyst, which indicates that the hydrogenation of S1 follows the 3/5-Meta pathway. See: Hopmann, K. H.; Bayer, A. Organometallics 2011, 30, 2483
    • (2011) Organometallics , vol.30 , pp. 2483
    • Hopmann, K.H.1    Bayer, A.2
  • 89
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    • version 7.0; Schrödinger, LLC: New York
    • Jaguar, version 7.0; Schrödinger, LLC: New York, 2010; http://www.schrodinger.com/.
    • (2010) Jaguar


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.