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Volumn 124, Issue 42, 2002, Pages 12426-12427

Non-carbonyl-stabilized metallocarbenoids in synthesis: The development of a tandem rhodium-catalyzed bamford-stevens/thermal aliphatic claisen rearrangement sequence

Author keywords

[No Author keywords available]

Indexed keywords

ALKANE; CARBENOID; CARBONYL DERIVATIVE; ETHER DERIVATIVE; METAL; RHODIUM;

EID: 0037164078     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja028020j     Document Type: Article
Times cited : (83)

References (26)
  • 1
    • 0000217402 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, Chapter 7.2
    • (a) Wipf, P. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, Chapter 7.2; p 827.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 827
    • Wipf, P.1
  • 10
    • 0001127813 scopus 로고
    • (a) For a thermal Bamford-Stevens reaction using an aziridinyl imine, see: Mohamadi, F.; Collum, D. B. Tetrahedron Lett. 1984, 25, 271. For Shapiro reactions of aziridinyl imines, see: (b) Maruoka, K.; Oishi, M.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 2289. (c) Evans, D. A.; Nelson, J. V. J. Am. Chem. Soc. 1980, 102, 774.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 271
    • Mohamadi, F.1    Collum, D.B.2
  • 11
    • 0029932282 scopus 로고    scopus 로고
    • (a) For a thermal Bamford-Stevens reaction using an aziridinyl imine, see: Mohamadi, F.; Collum, D. B. Tetrahedron Lett. 1984, 25, 271. For Shapiro reactions of aziridinyl imines, see: (b) Maruoka, K.; Oishi, M.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 2289. (c) Evans, D. A.; Nelson, J. V. J. Am. Chem. Soc. 1980, 102, 774.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 2289
    • Maruoka, K.1    Oishi, M.2    Yamamoto, H.3
  • 12
    • 0000448986 scopus 로고
    • (a) For a thermal Bamford-Stevens reaction using an aziridinyl imine, see: Mohamadi, F.; Collum, D. B. Tetrahedron Lett. 1984, 25, 271. For Shapiro reactions of aziridinyl imines, see: (b) Maruoka, K.; Oishi, M.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 2289. (c) Evans, D. A.; Nelson, J. V. J. Am. Chem. Soc. 1980, 102, 774.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 774
    • Evans, D.A.1    Nelson, J.V.2
  • 14
    • 0001589182 scopus 로고
    • N-aziridinyl imines in combination with catalysis have seen limited use. For examples, see: (a) Padwa, A.; Austin, D. J.; Gareau, Y.; Kassir, J. M.; Xu, S. L. J. Am. Chem. Soc. 1993, 115, 2637. (b) Sarkar, T. K.; Ghorai, B. K. J. Chem. Soc., Chem. Commun. 1992, 1184. (c) Fang, F. G.; Maier, M. E.; Danishefsky, S. J.; Schulte, G. J. Org. Chem. 1990, 55, 831.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 2637
    • Padwa, A.1    Austin, D.J.2    Gareau, Y.3    Kassir, J.M.4    Xu, S.L.5
  • 15
    • 37049076140 scopus 로고
    • N-aziridinyl imines in combination with catalysis have seen limited use. For examples, see: (a) Padwa, A.; Austin, D. J.; Gareau, Y.; Kassir, J. M.; Xu, S. L. J. Am. Chem. Soc. 1993, 115, 2637. (b) Sarkar, T. K.; Ghorai, B. K. J. Chem. Soc., Chem. Commun. 1992, 1184. (c) Fang, F. G.; Maier, M. E.; Danishefsky, S. J.; Schulte, G. J. Org. Chem. 1990, 55, 831.
    • (1992) J. Chem. Soc., Chem. Commun. , vol.1184
    • Sarkar, T.K.1    Ghorai, B.K.2
  • 16
    • 0025303985 scopus 로고
    • N-aziridinyl imines in combination with catalysis have seen limited use. For examples, see: (a) Padwa, A.; Austin, D. J.; Gareau, Y.; Kassir, J. M.; Xu, S. L. J. Am. Chem. Soc. 1993, 115, 2637. (b) Sarkar, T. K.; Ghorai, B. K. J. Chem. Soc., Chem. Commun. 1992, 1184. (c) Fang, F. G.; Maier, M. E.; Danishefsky, S. J.; Schulte, G. J. Org. Chem. 1990, 55, 831.
    • (1990) J. Org. Chem. , vol.55 , pp. 831
    • Fang, F.G.1    Maier, M.E.2    Danishefsky, S.J.3    Schulte, G.4
  • 17
    • 0010963938 scopus 로고    scopus 로고
    • note
    • All hydrazones were prepared from the corresponding ketones. See the Supporting Information.
  • 20
    • 0010968399 scopus 로고    scopus 로고
    • See refs 3b and 8b
    • (c) See refs 3b and 8b.


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