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Volumn 26, Issue , 2010, Pages 1-52

Asymmetric deprotonations using chiral lithium amide bases

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EID: 77958561091     PISSN: 0082500X     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Article
Times cited : (23)

References (219)
  • 35
    • 4444356831 scopus 로고    scopus 로고
    • For another enantioselective β-elimination using (R,R)-14, see
    • For another enantioselective β-elimination using (R,R)-14, see: (a) Nichols, C. J.; Simp-kins, N. S. Tetrahedron Lett. 2004, 45, 7469-7473;.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 7469-7473
    • Nichols, C.J.1    Simp-Kins, N.S.2
  • 49
    • 0035902862 scopus 로고    scopus 로고
    • Recently, magnesium bis-amides have been investigated as chiral bases for the asymmetric deprotonation of conformationally-locked cyclohexanones. For leading references: (a)
    • Recently, magnesium bis-amides have been investigated as chiral bases for the asymmetric deprotonation of conformationally-locked cyclohexanones. For leading references: (a) Henderson, K. W.; Kerr, W. J. Chem. Eur. J. 2001, 7, 3430-3437.
    • (2001) Chem. Eur. J. , vol.7 , pp. 3430-3437
    • Henderson, K.W.1    Kerr, W.J.2
  • 69
    • 15944363773 scopus 로고    scopus 로고
    • For an example where increasing the scale of the reaction led to a deterioration in er
    • For an example where increasing the scale of the reaction led to a deterioration in er: Clive, D. L. J.; Wang, H.; Yu, M. L. Tetrahedron Lett. 2005, 46, 2853-2855.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 2853-2855
    • Clive, D.L.J.1    Wang, H.2    Yu, M.L.3
  • 81
    • 0033525637 scopus 로고    scopus 로고
    • For an example where this chiral base was used in synthesis
    • For an example where this chiral base was used in synthesis: (b) Kirihara, M.; Nishio, T.; Yokoyama, S.; Kakuda, H.; Momose, T. Tetrahedron 1999, 55, 2911-2926.
    • (1999) Tetrahedron , vol.55 , pp. 2911-2926
    • Kirihara, M.1    Nishio, T.2    Yokoyama, S.3    Kakuda, H.4    Momose, T.5
  • 97
    • 0028360668 scopus 로고
    • (a) Wild, H. J. Org. Chem. 1994, 59, 2748-2761.
    • (1994) J. Org. Chem. , vol.59 , pp. 2748-2761
    • Wild, H.1
  • 125
  • 155
    • 0030583467 scopus 로고    scopus 로고
    • For examples of diastereoselective reactions of enolates using atropisomeric imides, see
    • For examples of diastereoselective reactions of enolates using atropisomeric imides, see: (b) Hughes, A. D.; Price D. A.; Shishkin, O.; Simpkins, N. S. Tetrahedron Lett. 1996, 37, 7607-7610.
    • (1996) Tetrahedron Lett. , Issue.37 , pp. 7607-7610
    • Hughes, A.D.1    Price, D.A.2    Shishkin, O.3    Simpkins, N.S.4
  • 186
    • 0003145073 scopus 로고    scopus 로고
    • Ariffin, A.; Blake, A. J.; Li, W. S.; Simpkins, N. S. Synlett 1997, 1453-1455.
    • (1997) Synlett , pp. 1453-1455
    • Ariffin, A.1    Blake, A.2
  • 205
    • 33746290163 scopus 로고    scopus 로고
    • For a review covering the applications of C3-symmetric ligands
    • For a review covering the applications of C3-symmetric ligands: Gibson, S. E.; Castaldi, M. P. Chem. Commun. 2006, 3045-3062.
    • (2006) Chem. Commun. , pp. 3045-3062
    • Gibson, S.E.1    Castaldi, M.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.