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Volumn 252, Issue 5-7, 2008, Pages 492-512

Stereoselective reactions involving hypervalent silicate complexes

Author keywords

Chiral Lewis bases; Hypervalent silicon center; Organic catalysts; Silyl reagents; Stereoselective reactions

Indexed keywords


EID: 39649097831     PISSN: 00108545     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ccr.2007.10.009     Document Type: Review
Times cited : (106)

References (109)
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    • See also in:
    • See also in:
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    • For reviews on recoverable and recyclable organic catalysts see:
    • For reviews on recoverable and recyclable organic catalysts see:
  • 13
    • 39649091529 scopus 로고    scopus 로고
    • Reviews about the formation and structure of hypervalent silicon compounds:
    • Reviews about the formation and structure of hypervalent silicon compounds:
  • 16
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    • Lukevics E., Pudova O., and Sturkovich R. (Eds), Ellis Horwood, Chichester
    • In: Lukevics E., Pudova O., and Sturkovich R. (Eds). Molecular Structure of Organosilicon Compounds (1989), Ellis Horwood, Chichester
    • (1989) Molecular Structure of Organosilicon Compounds
  • 21
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    • For a discussion about the possible involvement of heptacoordinated silicon species in nucleophilic addition to hexacoordinated silicon species, see ref [7a], p. 1240
    • Furin G.G., Vyazankina O.A., Gostevsky B.A., and Vyazankin N.S. Tetrahedron 44 (1988) 2675 For a discussion about the possible involvement of heptacoordinated silicon species in nucleophilic addition to hexacoordinated silicon species, see ref [7a], p. 1240
    • (1988) Tetrahedron , vol.44 , pp. 2675
    • Furin, G.G.1    Vyazankina, O.A.2    Gostevsky, B.A.3    Vyazankin, N.S.4
  • 27
    • 39649089724 scopus 로고    scopus 로고
    • Recently a bis lithium salt of 3,3′-dibromo-2,2′-binaphthol was employed to catalyse the aldol addition of a trimethoxysilyl enol ether to an aliphatic aldehyde, see:
    • Recently a bis lithium salt of 3,3′-dibromo-2,2′-binaphthol was employed to catalyse the aldol addition of a trimethoxysilyl enol ether to an aliphatic aldehyde, see:
  • 32
    • 39649089454 scopus 로고    scopus 로고
    • note
    • This mechanism hypothesis was later modified by the authors, which in successive publications propose a transition state more similar to that described by Malkov and Kocovsky (see below), where the silicon atom is not involved in the direct coordination of the substrate
  • 44
    • 39649085927 scopus 로고    scopus 로고
    • For a microreview about chiral N-oxides in asymmetric catalysis see:
    • For a microreview about chiral N-oxides in asymmetric catalysis see:
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    • 39649084747 scopus 로고    scopus 로고
    • See ref. [10] and
    • See ref. [10] and
  • 55
    • 39649083458 scopus 로고    scopus 로고
    • Review:
    • Review:
  • 71
    • 39649117423 scopus 로고    scopus 로고
    • For a review on silver catalyzed asymmetric allylation see:
    • For a review on silver catalyzed asymmetric allylation see:
  • 77
    • 39649099867 scopus 로고    scopus 로고
    • For an overview, see:
    • For an overview, see:
  • 80
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    • (and references cited there)
    • Denmark S.E., and Pham S.M. J. Org. Chem. 68 (2003) 5045 (and references cited there)
    • (2003) J. Org. Chem. , vol.68 , pp. 5045
    • Denmark, S.E.1    Pham, S.M.2
  • 88
    • 39649117858 scopus 로고    scopus 로고
    • See, for example:
    • See, for example:
  • 106
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    • For recent work appeared in the literature, see:
    • For recent work appeared in the literature, see:
  • 108
    • 39649100510 scopus 로고    scopus 로고
    • For a very recent contribution to the field:
    • For a very recent contribution to the field:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.