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Volumn 50, Issue 26, 2009, Pages 3458-3462

Organocatalytic enantioselective domino synthesis of highly functionalized cyclohexanes with an all-carbon quaternary stereocenter

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; CARBON; CYCLOHEXANE DERIVATIVE;

EID: 65549124146     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.02.209     Document Type: Article
Times cited : (34)

References (64)
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    • For an excellent paper on combining one-pot, step reduction and atom economy in organic chemistry see:. Clarke P.A., Santos S., and Martin W.H.C. Green Chem. 9 (2007) 438
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    • Clarke, P.A.1    Santos, S.2    Martin, W.H.C.3
  • 11
    • 33947198541 scopus 로고    scopus 로고
    • For excellent reviews on organocatalytic domino reactions see:
    • For excellent reviews on organocatalytic domino reactions see:. Enders D., Grondal C., and Hüttl M.R.M. Angew. Chem., Int. Ed. 46 (2007) 1570
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    • Enders, D.1    Grondal, C.2    Hüttl, M.R.M.3
  • 13
    • 2342614099 scopus 로고    scopus 로고
    • For selected examples of organocatalytic asymmetric domino and cascade reactions see:
    • For selected examples of organocatalytic asymmetric domino and cascade reactions see:. Halland N., Aburell P.S., and Jørgensen K.A. Angew. Chem., Int. Ed. 43 (2004) 1272
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 1272
    • Halland, N.1    Aburell, P.S.2    Jørgensen, K.A.3
  • 36
    • 0035905575 scopus 로고    scopus 로고
    • For selected reviews on quaternary stereocenters see:
    • For selected reviews on quaternary stereocenters see:. Christoffers J., and Mann A. Angew. Chem., Int. Ed. 40 (2001) 4591
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4591
    • Christoffers, J.1    Mann, A.2
  • 40
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    • To the best of our knowledge, there are only a few previous recent examples of the formation of an all-carbon stereocenter in chiral amine-catalyzed domino reactions see: Ref. 5w and
    • To the best of our knowledge, there are only a few previous recent examples of the formation of an all-carbon stereocenter in chiral amine-catalyzed domino reactions see: Ref. 5w and. Rios R., Sundén H., Vesely J., Zhao G.-L., Dziedzic P., and Córdova A. Adv. Synth. Catal. 349 (2007) 1028
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 1028
    • Rios, R.1    Sundén, H.2    Vesely, J.3    Zhao, G.-L.4    Dziedzic, P.5    Córdova, A.6
  • 44
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    • For an excellent review on organocatalytic Michael additions see:
    • For an excellent review on organocatalytic Michael additions see:. Sulzer Mossé S., and Alexakis A. Chem. Commun. (2007) 3123
    • (2007) Chem. Commun. , pp. 3123
    • Sulzer Mossé, S.1    Alexakis, A.2
  • 57
    • 65549170994 scopus 로고    scopus 로고
    • note
    • 6Na) requires m/z 355.0901, found 355.0897.
  • 58
    • 21244473265 scopus 로고    scopus 로고
    • Similar effects have been observed in organocatalytic Mannich-type reactions see:
    • Similar effects have been observed in organocatalytic Mannich-type reactions see:. Westermann B., and Neuhaus C. Angew. Chem., Int. Ed. 44 (2005) 4077
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 4077
    • Westermann, B.1    Neuhaus, C.2
  • 62
    • 65549101593 scopus 로고    scopus 로고
    • note
    • 4Na) requires m/z 344.0660, found 344.0657.
  • 63
    • 65549087459 scopus 로고    scopus 로고
    • note
    • 4Na) requires m/z 344.0660, found 344.0658.
  • 64
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    • note
    • CCDC 704580 contains the supplementary crystallographic data for this Letter. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.