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Volumn 9, Issue 20, 2007, Pages 3885-3887

[3+2] cycloaddition reactions of cyclopropyl imines with enones

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EID: 35048847434     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071376l     Document Type: Article
Times cited : (55)

References (30)
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    • Binger, P.; Büch, H. M. Cyclopropenes and Methylenecyclopropanes as Multifunctional Reagents in Transition Metal Catalyzed Reactions. In Topics in Current Chemistry; de Meijere, A., Ed.; Springer-Verlag: Berlin, Germany, 1987: 135, pp 109-131.
    • (a) Binger, P.; Büch, H. M. Cyclopropenes and Methylenecyclopropanes as Multifunctional Reagents in Transition Metal Catalyzed Reactions. In Topics in Current Chemistry; de Meijere, A., Ed.; Springer-Verlag: Berlin, Germany, 1987: Vol. 135, pp 109-131.
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    • and references cited therein
    • (d) Lautens, M.; Ren, Y. J. Am. Chem. Soc 1996, 118, 9597 and references cited therein.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 9597
    • Lautens, M.1    Ren, Y.2
  • 10
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    • For examples of oxidative addition to simple cyclopropanes, see: (a) Murakami, M, Ho, Y. Top. Organomet. Chem. 1999, 3, 97
    • For examples of oxidative addition to simple cyclopropanes, see: (a) Murakami, M.; Ho, Y. Top. Organomet. Chem. 1999, 3, 97.
  • 11
    • 33845376001 scopus 로고
    • For an illustration that C-H insertion precedes C-C bond cleavage, see
    • (b) For an illustration that C-H insertion precedes C-C bond cleavage, see: Periani, R. A.; Bergman, R. G. J. Am. Chem. Soc. 1986, 108, 7346.
    • (1986) J. Am. Chem. Soc , vol.108 , pp. 7346
    • Periani, R.A.1    Bergman, R.G.2
  • 12
    • 28044450635 scopus 로고    scopus 로고
    • For Lewis acid-mediated or nucleophile-promoted reactions of activated cyclopropanes processes, see: a
    • For Lewis acid-mediated or nucleophile-promoted reactions of activated cyclopropanes processes, see: (a) Pohlhaus, P. D.; Johnson, J. S. J. Am. Chem. Soc. 2005, 127, 16014.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 16014
    • Pohlhaus, P.D.1    Johnson, J.S.2
  • 21
    • 33750484992 scopus 로고    scopus 로고
    • For an insightful analysis of the work, see
    • (c) For an insightful analysis of the work, see: Lloyd-Jones, G. C. Angew. Chem., Int. Ed. 2006, 45, 6788.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 6788
    • Lloyd-Jones, G.C.1
  • 22
    • 4944241519 scopus 로고    scopus 로고
    • For examples of metallacyclic nickel enolates, see: (a) Hratchian, H. P, Chewdhury, S. K, Gutiérrez-García, V. M, Amarasinghe, K. K. D, Heeg, M. J, Schlegel, H. B, Montgomery, J. Organometallics 2004, 23, 4636
    • For examples of metallacyclic nickel enolates, see: (a) Hratchian, H. P.; Chewdhury, S. K.; Gutiérrez-García, V. M.; Amarasinghe, K. K. D.; Heeg, M. J.; Schlegel, H. B.; Montgomery, J. Organometallics 2004, 23, 4636.
  • 24
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    • For other catalytic reactions of cyclopropyl imines, see: a
    • For other catalytic reactions of cyclopropyl imines, see: (a) Kamatani, A.; Chatani, N.; Morimoto, T.; Murai, S. J. Org. Chem. 2000, 65, 9230.
    • (2000) J. Org. Chem , vol.65 , pp. 9230
    • Kamatani, A.1    Chatani, N.2    Morimoto, T.3    Murai, S.4
  • 26
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    • For examples of pyridine-directed C-C bond activation in a ketimine, see: (a) Jun, C.-H, Lee, H, Lim, S.-G. J. Am. Chem. Soc. 2001, 123, 751
    • For examples of pyridine-directed C-C bond activation in a ketimine, see: (a) Jun, C.-H.; Lee, H.; Lim, S.-G. J. Am. Chem. Soc. 2001, 123, 751.
  • 28
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    • For examples of imine- and oxime-directed C-H activation, see: (c) Desai, L. V, Hull, K. L, Sanford, M. S. J. Am. Chem. Soc. 2004, 126, 9542
    • For examples of imine- and oxime-directed C-H activation, see: (c) Desai, L. V.; Hull, K. L.; Sanford, M. S. J. Am. Chem. Soc. 2004, 126, 9542.
  • 30
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    • For conversion of a cyclopropyl imine to an enal as a minor side product of a reaction, see ref 7a
    • For conversion of a cyclopropyl imine to an enal as a minor side product of a reaction, see ref 7a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.