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Volumn 63, Issue 13, 1998, Pages 4338-4348

Highly Stereoselective Ylide Aziridination of N-Sulfonylimines with Sulfonium Propargylides: A Simple Way to Synthesize Scalemic Acetylenylaziridines

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EID: 0000264740     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9800964     Document Type: Article
Times cited : (75)

References (62)
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    • Reviews on the synthetic applications of chiral aziridines: (a) Tanner, D. Angew. Chem., Int. Ed. Engl. 1994, 33, 599. (b) Tanner, D. Pure Appl. Chem. 1993, 65, 1319. (c) Hudlicky, T.; Seoane, G.; Price, J. D.; Gadamasetti, K. G. Synlett 1990, 433.
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    • Tanner, D.1
  • 2
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    • Reviews on the synthetic applications of chiral aziridines: (a) Tanner, D. Angew. Chem., Int. Ed. Engl. 1994, 33, 599. (b) Tanner, D. Pure Appl. Chem. 1993, 65, 1319. (c) Hudlicky, T.; Seoane, G.; Price, J. D.; Gadamasetti, K. G. Synlett 1990, 433.
    • (1993) Pure Appl. Chem. , vol.65 , pp. 1319
    • Tanner, D.1
  • 3
    • 84986456216 scopus 로고
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    • (1990) Synlett , pp. 433
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  • 4
    • 0030907093 scopus 로고    scopus 로고
    • Recent reviews on asymmetric aziridination: (a) Osborn, H. M. I.; Sweeney, J. B. Tetrahedron, Asymmetry 1997, 8, 1693. (b) Li, A.-H.; Dai, L.-X. Chemistry (Chinese Chem. Soc., Taipei) 1996, 54 (4), 157-168 (in Chinese).
    • (1997) Tetrahedron, Asymmetry , vol.8 , pp. 1693
    • Osborn, H.M.I.1    Sweeney, J.B.2
  • 5
    • 0012198649 scopus 로고    scopus 로고
    • in Chinese
    • Recent reviews on asymmetric aziridination: (a) Osborn, H. M. I.; Sweeney, J. B. Tetrahedron, Asymmetry 1997, 8, 1693. (b) Li, A.-H.; Dai, L.-X. Chemistry (Chinese Chem. Soc., Taipei) 1996, 54 (4), 157-168 (in Chinese).
    • (1996) Chemistry (Chinese Chem. Soc., Taipei) , vol.54 , Issue.4 , pp. 157-168
    • Li, A.-H.1    Dai, L.-X.2
  • 41
    • 0001893022 scopus 로고    scopus 로고
    • For recent reviews: (c) Meyer, O.; Cagle, P. C.; Weickhardt, K.; Vichard, D.; Gladysz, J. A. Pure Appl. Chem. 1996, 68, 79. (d) Li, A.-H.; Dai, L.-X.; Aggarwal, V. K. Chem. Rev. 1997, 97, 2431.
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    • Li, A.-H.1    Dai, L.-X.2    Aggarwal, V.K.3
  • 42
    • 0000793191 scopus 로고
    • For epoxidation: (a) Zhou, Z.-L.; Huang, Y.-Z.; Shi, L.-L.; Hu, J. J. Org. Chem. 1992, 57, 6598. For cyclopropanation: (b) Liao, Q.-M. Ph.D. Thesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China, 1989.
    • (1992) J. Org. Chem. , vol.57 , pp. 6598
    • Zhou, Z.-L.1    Huang, Y.-Z.2    Shi, L.-L.3    Hu, J.4
  • 43
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    • Ph.D. Thesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China
    • For epoxidation: (a) Zhou, Z.-L.; Huang, Y.-Z.; Shi, L.-L.; Hu, J. J. Org. Chem. 1992, 57, 6598. For cyclopropanation: (b) Liao, Q.-M. Ph.D. Thesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China, 1989.
    • (1989)
    • Liao, Q.-M.1
  • 49
    • 0001724430 scopus 로고
    • Two reports on the rearrangement of an acetylenyl-substituted vinylaziridine from a multistep sequence: (a) Manisse, N.; Chuche, J. Tetrahedron 1977, 33, 2399. (b) Manisse, N.; Chuche, J. J. Am. Chem. Soc. 1977, 99, 1272.
    • (1977) Tetrahedron , vol.33 , pp. 2399
    • Manisse, N.1    Chuche, J.2
  • 50
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    • Two reports on the rearrangement of an acetylenyl-substituted vinylaziridine from a multistep sequence: (a) Manisse, N.; Chuche, J. Tetrahedron 1977, 33, 2399. (b) Manisse, N.; Chuche, J. J. Am. Chem. Soc. 1977, 99, 1272.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 1272
    • Manisse, N.1    Chuche, J.2


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