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Volumn , Issue 21, 2003, Pages 2712-2713

Chiral sulfoxides in the enantioselective allylation of aldehydes with allyltrichlorosilane

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALLYL TRICHLOROSILANE; BASE; LEWIS BASE; SILANE DERIVATIVE; SULFOXIDE; UNCLASSIFIED DRUG;

EID: 0242609866     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b309704h     Document Type: Article
Times cited : (71)

References (24)
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    • (2002)
    • Kentish-Barnes, W.1
  • 11
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    • During the preparation of this manuscript two reports appeared in the literature detailing the use of sulfoxides in the allylation reactions: (a) S. Kobayashi, C. Ogawa, H. Konishi and M. Sugiura, J. Am. Chem. Soc., 2003, 125, 6610; (b) A. Massa, A. V. Malkov, P. Kocovsky and A. Scettri, Tetrahedron Lett., 2003, 44, 7179.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6610
    • Kobayashi, S.1    Ogawa, C.2    Konishi, H.3    Sugiura, M.4
  • 12
    • 0041508449 scopus 로고    scopus 로고
    • During the preparation of this manuscript two reports appeared in the literature detailing the use of sulfoxides in the allylation reactions: (a) S. Kobayashi, C. Ogawa, H. Konishi and M. Sugiura, J. Am. Chem. Soc., 2003, 125, 6610; (b) A. Massa, A. V. Malkov, P. Kocovsky and A. Scettri, Tetrahedron Lett., 2003, 44, 7179.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 7179
    • Massa, A.1    Malkov, A.V.2    Kocovsky, P.3    Scettri, A.4
  • 17
    • 33845550636 scopus 로고
    • Derivatives prepared by modification of the procedures from: J. K. Whitesell and D. Reynolds, J. Org. Chem., 1983, 48, 3548; I. Chataigner, J. Lebreton, D. Durand, A. Guingant and J. Villiéras, Tetrahedron Lett., 1998, 39, 1759.
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    • Whitesell, J.K.1    Reynolds, D.2
  • 19
    • 0030013323 scopus 로고    scopus 로고
    • Literature values taken from: F. Bracher and T. Litz, Bioorg. Med. Chem., 1996, 4, 877; E. J. Corey and S. S. Kim, Tetrahedron Lett., 1990, 31, 3715; S. E. Denmark, D. M. Coe, N. E. Pratt and B. D. Griedel, J. Org. Chem., 1994, 59, 6161; T.-P. Loh, J.-R. Zhou and Z. Yin, Org. Lett., 1999, 1, 1855.
    • (1996) Bioorg. Med. Chem. , vol.4 , pp. 877
    • Bracher, F.1    Litz, T.2
  • 20
    • 0025370315 scopus 로고
    • Literature values taken from: F. Bracher and T. Litz, Bioorg. Med. Chem., 1996, 4, 877; E. J. Corey and S. S. Kim, Tetrahedron Lett., 1990, 31, 3715; S. E. Denmark, D. M. Coe, N. E. Pratt and B. D. Griedel, J. Org. Chem., 1994, 59, 6161; T.-P. Loh, J.-R. Zhou and Z. Yin, Org. Lett., 1999, 1, 1855.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 3715
    • Corey, E.J.1    Kim, S.S.2
  • 21
    • 33751157465 scopus 로고
    • Literature values taken from: F. Bracher and T. Litz, Bioorg. Med. Chem., 1996, 4, 877; E. J. Corey and S. S. Kim, Tetrahedron Lett., 1990, 31, 3715; S. E. Denmark, D. M. Coe, N. E. Pratt and B. D. Griedel, J. Org. Chem., 1994, 59, 6161; T.-P. Loh, J.-R. Zhou and Z. Yin, Org. Lett., 1999, 1, 1855.
    • (1994) J. Org. Chem. , vol.59 , pp. 6161
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  • 22
    • 0000162932 scopus 로고    scopus 로고
    • Literature values taken from: F. Bracher and T. Litz, Bioorg. Med. Chem., 1996, 4, 877; E. J. Corey and S. S. Kim, Tetrahedron Lett., 1990, 31, 3715; S. E. Denmark, D. M. Coe, N. E. Pratt and B. D. Griedel, J. Org. Chem., 1994, 59, 6161; T.-P. Loh, J.-R. Zhou and Z. Yin, Org. Lett., 1999, 1, 1855.
    • (1999) Org. Lett. , vol.1 , pp. 1855
    • Loh, T.-P.1    Zhou, J.-R.2    Yin, Z.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.