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Volumn 10, Issue 19, 2008, Pages 4231-4234

Cu(I)-catalyzed asymmetric diamination of conjugated dienes

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; COPPER; DIAMINE; LIGAND;

EID: 55449137856     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol801605w     Document Type: Article
Times cited : (99)

References (51)
  • 4
    • 33847087811 scopus 로고    scopus 로고
    • For examples of metal-mediated diaminations, see: Co: (a) Becker, P. N, White, M. A, Bergman, R. G. J. Am. Chem. Soc. 1980, 102, 5676
    • For examples of metal-mediated diaminations, see: Co: (a) Becker, P. N.; White, M. A.; Bergman, R. G. J. Am. Chem. Soc. 1980, 102, 5676.
  • 11
    • 23844527400 scopus 로고    scopus 로고
    • For recent Cu(II)-mediated intramolecular diamination, see: (a) Zabawa, T. P.; Kasi, D.; Chemler, S. R. J. Am. Chem. Soc. 2005, 127, 11250.
    • For recent Cu(II)-mediated intramolecular diamination, see: (a) Zabawa, T. P.; Kasi, D.; Chemler, S. R. J. Am. Chem. Soc. 2005, 127, 11250.
  • 13
    • 0035915127 scopus 로고    scopus 로고
    • 2, see: (a) Li, G.; Wei, H.-X.; Kim, S. H.; Carducci, M. D. Angew. Chem., Int. Ed. 2001, 40, 4277.
    • 2, see: (a) Li, G.; Wei, H.-X.; Kim, S. H.; Carducci, M. D. Angew. Chem., Int. Ed. 2001, 40, 4277.
  • 15
    • 19744362485 scopus 로고    scopus 로고
    • For a recent Pd(II)-catalyzed intermolecular diamination of conjugated dienes, see: Bar, G. L. J.; Lloyd-Jones, G. C.; Booker-Milburn, K. I. J. Am. Chem. Soc. 2005, 127, 7308.
    • For a recent Pd(II)-catalyzed intermolecular diamination of conjugated dienes, see: Bar, G. L. J.; Lloyd-Jones, G. C.; Booker-Milburn, K. I. J. Am. Chem. Soc. 2005, 127, 7308.
  • 16
    • 27144440348 scopus 로고    scopus 로고
    • For recent Pd(II)- and Ni-catalyzed intramolecular diamination of olefins, see: (a) Streuff, J.; Hövelmann, C. H.; Nieger, M.; Muñiz, K. J. Am. Chem. Soc. 2005, 127, 14586.
    • For recent Pd(II)- and Ni-catalyzed intramolecular diamination of olefins, see: (a) Streuff, J.; Hövelmann, C. H.; Nieger, M.; Muñiz, K. J. Am. Chem. Soc. 2005, 127, 14586.
  • 20
    • 33846624362 scopus 로고    scopus 로고
    • For Pd(0)-catalyzed intermolecular diamination, see: (a) Du, H.; Zhao, B.; Shi, Y. J. Am. Chem. Soc. 2007, 129, 762.
    • For Pd(0)-catalyzed intermolecular diamination, see: (a) Du, H.; Zhao, B.; Shi, Y. J. Am. Chem. Soc. 2007, 129, 762.
  • 23
    • 34547198807 scopus 로고    scopus 로고
    • For Cu(I)-catalyzed intermolecular diamination, see: (a) Yuan, W.; Du, H.; Zhao, B.; Shi, Y. Org. Lett. 2007, 9, 2589.
    • For Cu(I)-catalyzed intermolecular diamination, see: (a) Yuan, W.; Du, H.; Zhao, B.; Shi, Y. Org. Lett. 2007, 9, 2589.
  • 26
    • 0037281853 scopus 로고    scopus 로고
    • For leading references on asymmetric diamination using bisimi-doosmium as reagent, see: a
    • For leading references on asymmetric diamination using bisimi-doosmium as reagent, see: (a) Muniz, K.; Nieger, M. Synlett 2003, 211.
    • (2003) Synlett , pp. 211
    • Muniz, K.1    Nieger, M.2
  • 32
    • 0003593740 scopus 로고
    • For a leading review on diaziridinone, see:, Hassner, A, Ed, John Wiley & Sons, Inc, Hoboken, NJ
    • For a leading review on diaziridinone, see: Heine, H. W. In The Chemistry of Heterocyclic Compounds; Hassner, A., Ed.; John Wiley & Sons, Inc.: Hoboken, NJ, 1983; p 547.
    • (1983) The Chemistry of Heterocyclic Compounds , pp. 547
    • Heine, H.W.1
  • 33
    • 0000414557 scopus 로고
    • For a leading review on metal-promoted radical reactions, see
    • For a leading review on metal-promoted radical reactions, see: Iqbal, J.; Bhatia, B.; Nayyar, N. K. Chem. Rev. 1994, 94, 519.
    • (1994) Chem. Rev , vol.94 , pp. 519
    • Iqbal, J.1    Bhatia, B.2    Nayyar, N.K.3
  • 34
    • 0032732016 scopus 로고    scopus 로고
    • For leading reviews on CuX-catalyzed atom transfer reactions see: a
    • For leading reviews on CuX-catalyzed atom transfer reactions see: (a) Patten, T. E.; Matyjaszewski, K. Acc. Chem. Res. 1999, 32, 895.
    • (1999) Acc. Chem. Res , vol.32 , pp. 895
    • Patten, T.E.1    Matyjaszewski, K.2
  • 36
    • 0001253023 scopus 로고    scopus 로고
    • For a leading review on nitrogen-centered radicals, see:, Renaud, P, Sibi, M. P, Eds, Wiley-VCH: Weinheim, Germany
    • For a leading review on nitrogen-centered radicals, see: Stella, L. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, Germany, 2001; Vol. 2, p 407.
    • (2001) Radicals in Organic Synthesis , vol.2 , pp. 407
    • Stella, L.1
  • 37
    • 61349172040 scopus 로고    scopus 로고
    • For leading references on L1-L6, see: (a) Hattori, T.; Shijo, M.; Kumagai, S.; Miyano, S. Chem. Express 1991, 6, 335.
    • For leading references on L1-L6, see: (a) Hattori, T.; Shijo, M.; Kumagai, S.; Miyano, S. Chem. Express 1991, 6, 335.
  • 38
    • 61349134941 scopus 로고    scopus 로고
    • Ref 10a
    • (b) Ref 10a.
  • 44
    • 33947089148 scopus 로고    scopus 로고
    • For leading references on L7-L12, see: (a) Kagan, H. B.; Dang, T.-P. J. Am. Chem. Soc. 1972, 94, 6429.
    • For leading references on L7-L12, see: (a) Kagan, H. B.; Dang, T.-P. J. Am. Chem. Soc. 1972, 94, 6429.
  • 50
    • 61349174102 scopus 로고    scopus 로고
    • 1H NMR, and the ee's were determined by chiral HPLC.
    • 1H NMR, and the ee's were determined by chiral HPLC.
  • 51
    • 61349112198 scopus 로고    scopus 로고
    • The same conditions as ref 18 except for L7-L12 (0.01 mmol).
    • The same conditions as ref 18 except for L7-L12 (0.01 mmol).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.