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Volumn 11, Issue 15, 2009, Pages 3462-3465

Selective C - S bond formation via Fe-catalyzed allylic substitution

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EID: 68149144262     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901297s     Document Type: Article
Times cited : (109)

References (43)
  • 2
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    • Pd-catalyzed allylic sulfonation: (a) review: Gais, H.-J. In Asymmetric Synthesis with Chemical and Biological Methods; Enders, D., Jäger, K.-E., Eds.; Wiley-VCH: Weinheim, Germany, 2007; p 275.
    • Pd-catalyzed allylic sulfonation: (a) review: Gais, H.-J. In Asymmetric Synthesis with Chemical and Biological Methods; Enders, D., Jäger, K.-E., Eds.; Wiley-VCH: Weinheim, Germany, 2007; p 275.
  • 17
    • 0027074704 scopus 로고    scopus 로고
    • Allylic sulfenylations: Pd-catalyzed: (a) Goux, C.; Lhoste, P.; Sinou, D. Tetrahedron Lett. 1992, 33, 8099.
    • Allylic sulfenylations: Pd-catalyzed: (a) Goux, C.; Lhoste, P.; Sinou, D. Tetrahedron Lett. 1992, 33, 8099.
  • 25
    • 33845374037 scopus 로고    scopus 로고
    • For the use of sulfones possessing an acidic α-C-H bond see :(a) Fuchs, P. L.; Braish, T. F. Chem. Rev. 1986, 86, 903.
    • For the use of sulfones possessing an acidic α-C-H bond see :(a) Fuchs, P. L.; Braish, T. F. Chem. Rev. 1986, 86, 903.
  • 26
    • 0004139460 scopus 로고
    • Patai, S, Rapoport, Z, Stirling, C. J. M, Eds, John Wiley and Sons Ltd, Chichester, UK
    • (b) Grossed, J. S. In The Chemistry of Sulphones and Sulphoxides; Patai, S., Rapoport, Z., Stirling, C. J. M., Eds.; John Wiley and Sons Ltd.: Chichester, UK, 1988.
    • (1988) The Chemistry of Sulphones and Sulphoxides
    • Grossed, J.S.1
  • 27
    • 68149151878 scopus 로고    scopus 로고
    • Simpkins, N. S. Sulphones in Organic Synthesis; Pergamon Press: Oxford, UK, 1993.
    • (c) Simpkins, N. S. Sulphones in Organic Synthesis; Pergamon Press: Oxford, UK, 1993.
  • 28
    • 0037038993 scopus 로고    scopus 로고
    • For an excellent review on Julia-olefinations see
    • (d) For an excellent review on Julia-olefinations see: Blakemore, P. R. J. Chem. Soc., Perkin Trans. 1 2002, 2563.
    • (2002) J. Chem. Soc., Perkin Trans. 1 , pp. 2563
    • Blakemore, P.R.1
  • 29
    • 1342317039 scopus 로고    scopus 로고
    • For a recent review on the Ramberg-Backlund reaction see
    • (e) For a recent review on the Ramberg-Backlund reaction see: Taylor, R. J. K.; Casy, G. Org. React. 2003, 62, 357.
    • (2003) Org. React , vol.62 , pp. 357
    • Taylor, R.J.K.1    Casy, G.2
  • 30
    • 12344296105 scopus 로고    scopus 로고
    • A variety of transformations using sulfones lacking an acidic α-C-H bond have been reported, e.g., conjugate addition of Grignard reagents: (a) Julia, M.; Righini, A.; Verpeaux, J.-N. Tetrahedron 1979, 26, 2393.
    • A variety of transformations using sulfones lacking an acidic α-C-H bond have been reported, e.g., conjugate addition of Grignard reagents: (a) Julia, M.; Righini, A.; Verpeaux, J.-N. Tetrahedron 1979, 26, 2393.
  • 35
    • 0000242816 scopus 로고
    • 5216. ipso-substitution of allyl sulfones
    • (f) Trost, B. M.; Medic, C. A. J. Am. Chem. Soc. 1988, 110, 5216. ipso-substitution of allyl sulfones:
    • (1988) J. Am. Chem. Soc , vol.110
    • Trost, B.M.1    Medic, C.A.2
  • 36
  • 42
    • 33750950658 scopus 로고    scopus 로고
    • Although not in the focus of the present study vinyl sulfones are imporant building blocks in medicinal chemistry, for a review see: Meadows, D. C, Gervay-Hague, J. Med. Res. Rev. 2006, 26, 793. Investigations on the scope of the allylic sulfonation, isomerization are currently being carried out in our laboratories
    • Although not in the focus of the present study vinyl sulfones are imporant building blocks in medicinal chemistry, for a review see: Meadows, D. C.; Gervay-Hague, J. Med. Res. Rev. 2006, 26, 793. Investigations on the scope of the allylic sulfonation - isomerization are currently being carried out in our laboratories.
  • 43
    • 70349786223 scopus 로고    scopus 로고
    • A metal-by-metal displacement was observed in the related Rhcatalyzed allylic substitution: Wucher, B.; Moser, M.; Schumacher, S. A.; Rominger, F.; Kunz, D. Angew. Chem., Int. Ed. 2009, 48, 4417.
    • A metal-by-metal displacement was observed in the related Rhcatalyzed allylic substitution: Wucher, B.; Moser, M.; Schumacher, S. A.; Rominger, F.; Kunz, D. Angew. Chem., Int. Ed. 2009, 48, 4417.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.