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Volumn 137, Issue 1, 2015, Pages 383-389

Organocatalytic asymmetric synthesis of 1,1-diarylethanes by transfer hydrogenation

Author keywords

[No Author keywords available]

Indexed keywords

CELL CULTURE; HYDROGENATION;

EID: 84921022287     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja510980d     Document Type: Article
Times cited : (246)

References (95)
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    • For a leading example of the use of a hydroxyl directing group in chiral acid catalysis, see
    • For a leading example of the use of a hydroxyl directing group in chiral acid catalysis, see: Akiyama, T.; Morita, H.; Fuchibe, K. J. Am. Chem. Soc. 2006, 128, 13070-13071
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    • Akiyama, T.1    Morita, H.2    Fuchibe, K.3
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    • Sundberg, R. J. Indoles; Academic Press: London, 1996.
    • (1996) Indoles
    • Sundberg, R.J.1
  • 86
    • 46949083787 scopus 로고    scopus 로고
    • A similar interaction has also been proposed before. See
    • A similar interaction has also been proposed before. See: Simón, L.; Goodman, J. M. J. Am. Chem. Soc. 2008, 130, 8741-8747
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 8741-8747
    • Simón, L.1    Goodman, J.M.2
  • 87
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    • In a parallel study in our lab, the asymmetric substitution of such tertiary alcohols by indoles was achieved. See
    • In a parallel study in our lab, the asymmetric substitution of such tertiary alcohols by indoles was achieved. See: Zhao, W.; Wang, Z.; Chu, B.; Sun, J. Angew. Chem., Int. Ed. 2014, 10.1002/anie.201405252
    • (2014) Angew. Chem., Int. Ed.
    • Zhao, W.1    Wang, Z.2    Chu, B.3    Sun, J.4
  • 88
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    • We are aware of only one report on catalytic asymmetric reactions of p -QMs with high enantioselectivity, which deals with δ- monosubstituted p -QMs. See
    • We are aware of only one report on catalytic asymmetric reactions of p -QMs with high enantioselectivity, which deals with δ- monosubstituted p -QMs. See: Chu, W.-D.; Zhang, L.-F.; Bao, X.; Zhao, X.-H.; Zeng, C.; Du, J.-Y.; Zhang, G.-B.; Wang, F.-X.; Ma, X.-Y.; Fan, C.-A. Angew. Chem., Int. Ed. 2013, 52, 9229-9233
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 9229-9233
    • Chu, W.-D.1    Zhang, L.-F.2    Bao, X.3    Zhao, X.-H.4    Zeng, C.5    Du, J.-Y.6    Zhang, G.-B.7    Wang, F.-X.8    Ma, X.-Y.9    Fan, C.-A.10
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    • Terada and co-workers pioneered asymmetric nucleophilic addition to 3-vinylindoles to form indol-3-yl tertiary stereocenters. See
    • Terada and co-workers pioneered asymmetric nucleophilic addition to 3-vinylindoles to form indol-3-yl tertiary stereocenters. See: Terada, M.; Moriya, K.; Kanomata, K.; Sorimachi, K. Angew. Chem., Int. Ed. 2011, 50, 12586-12590
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 12586-12590
    • Terada, M.1    Moriya, K.2    Kanomata, K.3    Sorimachi, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.