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Volumn 6, Issue , 2012, Pages 214-233

6.8 Allylations of C-O and C-N Double Bonds and Related Reactions

Author keywords

Allylation; Allylboronate; Allyltrichlorosilane; Aminoallylation; Chiral Br nsted acid; Chiral diol; Homoallylic alcohol; Homoallylic amine; Lewis base catalyst

Indexed keywords


EID: 84890518435     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-0-08-095167-6.00608-X     Document Type: Chapter
Times cited : (2)

References (113)
  • 5
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    • For allylation of C-O double bonds, see:
    • Denmark S.E., Fu J. Chem. Rev. 2003, 103:2763-2793. For allylation of C-O double bonds, see:.
    • (2003) Chem. Rev. , vol.103 , pp. 2763-2793
    • Denmark, S.E.1    Fu, J.2
  • 9
    • 0038106171 scopus 로고    scopus 로고
    • Bloch R. Chem. Rev. 1998, 98:1407-1438.
    • (1998) Chem. Rev. , vol.98 , pp. 1407-1438
    • Bloch, R.1
  • 32
    • 33644532245 scopus 로고    scopus 로고
    • For a synthetic application, see:
    • Denmark S.E., Fu J., Lawler M.J. J. Org. Chem. 2006, 71:1523-1536. For a synthetic application, see:.
    • (2006) J. Org. Chem. , vol.71 , pp. 1523-1536
    • Denmark, S.E.1    Fu, J.2    Lawler, M.J.3
  • 76
    • 77953769716 scopus 로고    scopus 로고
    • Chiral sulfoxide 34 was first utilized as a Lewis base catalyst for allylation of N-acylhydrazones (see equation 9 and Reference 28)
    • De Sio C., Massa A., Scetti A. Org. Biomol. Chem. 2010, 8:3055-3059. Chiral sulfoxide 34 was first utilized as a Lewis base catalyst for allylation of N-acylhydrazones (see equation 9 and Reference 28).
    • (2010) Org. Biomol. Chem. , vol.8 , pp. 3055-3059
    • De Sio, C.1    Massa, A.2    Scetti, A.3
  • 81
    • 0037073229 scopus 로고    scopus 로고
    • See Refeference 11e. Formation of O-silylated chlorohydrins was confirmed for the first time in chiral phosphoramide-catalyzed, tetrachlorosilane-promoted addition of silyl ketene acetals to aldehydes, see:
    • Denmark S.E., Wynn T., Beutner G.L. J. Am. Chem. Soc. 2002, 124:13405-13407. See Refeference 11e. Formation of O-silylated chlorohydrins was confirmed for the first time in chiral phosphoramide-catalyzed, tetrachlorosilane-promoted addition of silyl ketene acetals to aldehydes, see:.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13405-13407
    • Denmark, S.E.1    Wynn, T.2    Beutner, G.L.3
  • 82
    • 76849102439 scopus 로고    scopus 로고
    • For a quantum-chemical study for the DMF- and HMPA-catalyzed allylation, see:, For computational analyses for enantioselective catalysis, see: References 5b, 11e, 13i, 15e.
    • Sakata K., Fujimoto H. Organometallics 2010, 29:1004-1011. For a quantum-chemical study for the DMF- and HMPA-catalyzed allylation, see:, For computational analyses for enantioselective catalysis, see: References 5b, 11e, 13i, 15e.
    • (2010) Organometallics , vol.29 , pp. 1004-1011
    • Sakata, K.1    Fujimoto, H.2
  • 97
    • 0041910844 scopus 로고    scopus 로고
    • 3CN was also reported. But no enantioselective catalysis of this reaction has been revealed. See: Wu, P.; Sun, J. Synth. Commun. 2008, 38, 1003-1010.
    • 3CN was also reported. But no enantioselective catalysis of this reaction has been revealed. See: Wu, P.; Sun, J. Synth. Commun. 2008, 38, 1003-1010.
    • (2003) Synlett , pp. 1749-1751
    • Sugiura, M.1    Robvieux, F.2    Kobayashi, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.