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Volumn 7, Issue 17, 2005, Pages 3681-3684

Ruthenium-catalyzed [2 + 2] cycloadditions of ynamides

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EID: 24044461397     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0512841     Document Type: Article
Times cited : (99)

References (78)
  • 1
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    • For reviews of the chemistry of ynamines and ynamides, see: (a) Ficini, J. Tetrahedron 1976, 32, 1448.
    • (1976) Tetrahedron , vol.32 , pp. 1448
    • Ficini, J.1
  • 34
    • 0001090792 scopus 로고    scopus 로고
    • For our recent contibutions on non-metal-catalyzed cycloaddition reactions of bicyclic alkenes, see: (a) Yip, C.; Handerson, S.; Jordan, R.; Tam, W. Org. Lett. 1999, 1, 791.
    • (1999) Org. Lett. , vol.1 , pp. 791
    • Yip, C.1    Handerson, S.2    Jordan, R.3    Tam, W.4
  • 40
    • 0000685077 scopus 로고    scopus 로고
    • For our recent contributions on Ru-catalyzed [2 + 2] cycloadditions, see: (a) Jordan, R. W.; Tam, W. Org. Lett. 2000, 2, 3031.
    • (2000) Org. Lett. , vol.2 , pp. 3031
    • Jordan, R.W.1    Tam, W.2
  • 47
    • 0002110351 scopus 로고    scopus 로고
    • For reviews on transition metal-catalyzed cycloadditions, see: (a) Lautens, M.; Klute, W.; Tam, W. Chem. Rev. 1996, 96, 49.
    • (1996) Chem. Rev. , vol.96 , pp. 49
    • Lautens, M.1    Klute, W.2    Tam, W.3
  • 53
    • 0001216151 scopus 로고    scopus 로고
    • Jabosen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Berlin
    • (d) Buchwald, S. L.; Hicks, F. A. In Comprehensive Asymmetric Catalysis I-III; Jabosen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Berlin, 1999; Vol. 2, pp 491-510.
    • (1999) Comprehensive Asymmetric Catalysis I-III , vol.2 , pp. 491-510
    • Buchwald, S.L.1    Hicks, F.A.2
  • 76
    • 33645590590 scopus 로고    scopus 로고
    • see our previous work in ref 17
    • For determination of the exo and endo stereochemistry of [2 + 2] cycloadducts, see our previous work in ref 17.
  • 77
    • 33645599974 scopus 로고    scopus 로고
    • note
    • Known chiral ynamides 10a and 10d were prepared according to Hsung's method; see ref 3b. The new chiral ynamides 10e and 10f were synthesized using Danheiser's method; see Supporting Information for details. The new chiral ynamide 10b was synthesized using the same method as per the synthesis of acyclic ynamides 3a-1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.