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Volumn 254, Issue 17-18, 2010, Pages 2007-2030

Use of sugar-based ligands in selective catalysis: Recent developments

Author keywords

Asymmetric; Carbohydrate based ligands; Catalysis; Enantioselectivity

Indexed keywords


EID: 77954383638     PISSN: 00108545     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ccr.2010.03.005     Document Type: Review
Times cited : (98)

References (295)
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    • Key major reviews:
    • Key major reviews:.
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    • For a more recent review concentrating on ligand donor type in the period (up to 2006) see
    • For a more recent review concentrating on ligand donor type in the period (up to 2006) see:.
  • 9
    • 77954383900 scopus 로고    scopus 로고
    • See for instance
    • See for instance:.
  • 10
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    • Wiley-VCH, Weinheim, I. Ojima (Ed.)
    • Catalytic Asymmetric Synthesis 2000, Wiley-VCH, Weinheim. 2nd ed. I. Ojima (Ed.).
    • (2000) Catalytic Asymmetric Synthesis
  • 47
    • 77954386850 scopus 로고    scopus 로고
    • For related water soluble rhodium complexes, see
    • For related water soluble rhodium complexes, see:.
  • 50
    • 77954385868 scopus 로고    scopus 로고
    • The water soluble deprotected-hydroxyl diphosphinite ligand 10 provides enantioselectivities up to 99%, see
    • The water soluble deprotected-hydroxyl diphosphinite ligand 10 provides enantioselectivities up to 99%, see:.
  • 125
    • 77954385690 scopus 로고    scopus 로고
    • Recently this concept has also been use to explain the chiral induction by the Trost ligand, see:
    • Recently this concept has also been use to explain the chiral induction by the Trost ligand, see:.
  • 127
    • 77954387520 scopus 로고    scopus 로고
    • See, for example:
    • See, for example:.
  • 130
    • 77954384158 scopus 로고    scopus 로고
    • See, for example:
    • See, for example:.
  • 134
    • 77954387556 scopus 로고    scopus 로고
    • Acc. Chem. Res. doi:10.1021/ar9002152
    • M. Diéguez, O. Pàmies, Acc. Chem. Res. doi:10.1021/ar9002152.
    • Diéguez, M.1    Pàmies, O.2
  • 135
    • 77954385901 scopus 로고    scopus 로고
    • The flexibility that the biaryl moiety offers can be used to fine-tune the chiral pocket formed upon complexation. See, for example:
    • The flexibility that the biaryl moiety offers can be used to fine-tune the chiral pocket formed upon complexation. See, for example:.
  • 139
    • 77954384955 scopus 로고    scopus 로고
    • See, for example:
    • See, for example:.
  • 157
    • 77954383944 scopus 로고    scopus 로고
    • See for instance:
    • See for instance:.
  • 179
    • 77954386588 scopus 로고    scopus 로고
    • For related water soluble ligands, see:
    • For related water soluble ligands, see:.
  • 201
    • 77954385556 scopus 로고    scopus 로고
    • For reviews see:
    • For reviews see:.
  • 208
    • 77954382817 scopus 로고    scopus 로고
    • See for instance:
    • See for instance:.
  • 227
    • 77954384220 scopus 로고    scopus 로고
    • See for example:
    • See for example:.
  • 230
    • 77954384775 scopus 로고    scopus 로고
    • Springer, Berlin, (Chapter 11, 382), E.N. Jacobsen, A. Pfaltz, H. Yamamoto (Eds.)
    • Nozaki K. Comprehensive Asymmetric Catalysis 1999, Springer, Berlin, (Chapter 11, 382). E.N. Jacobsen, A. Pfaltz, H. Yamamoto (Eds.).
    • (1999) Comprehensive Asymmetric Catalysis
    • Nozaki, K.1
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    • See for example:
    • See for example:.
  • 235
    • 0004147148 scopus 로고    scopus 로고
    • Kluwer Academic Press, Dordrecht, P.W.N.M. van Leeuwen, C. Claver (Eds.)
    • Rhodium Catalysed Hydroformylation 2000, Kluwer Academic Press, Dordrecht. P.W.N.M. van Leeuwen, C. Claver (Eds.).
    • (2000) Rhodium Catalysed Hydroformylation
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    • See for example:
    • See for example:.
  • 239
    • 77954386768 scopus 로고    scopus 로고
    • See for instance:
    • See for instance:.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.