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Volumn 69, Issue 8, 2004, Pages 2755-2759

Radical Carboazidation: Expedient Assembly of the Core Structure of Various Alkaloid Families

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; CARBON; KETONES; OLEFINS;

EID: 1842789823     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo035843y     Document Type: Article
Times cited : (83)

References (33)
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    • (2001) Radicals in Organic Synthesis
  • 3
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    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 715
    • Curran, D.P.1
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    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim
    • Byers, J. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 1; p 72.
    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 72
    • Byers, J.1
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    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim
    • Stella, L. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 2; p 407.
    • (2001) Radicals in Organic Synthesis , vol.2 , pp. 407
    • Stella, L.1
  • 12
  • 16
    • 0002273958 scopus 로고    scopus 로고
    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim
    • (d) Barton, D. H. R.; Jaszberenyi, J. Cs.; Theodorakis, E. A.; Reibenspies, J. H. J. Am. Chem. Soc. 1993, 115, 8050. For an exhaustive review, see: Ollivier, C.; Renaud P. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 2, p 93.
    • (2001) Radicals in Organic Synthesis , vol.2 , pp. 93
    • Ollivier, C.1    Renaud, P.2
  • 19
    • 0000058897 scopus 로고
    • Kiefer, H.; Traylor, T. G. Tetrahedron Lett. 1966, 49, 6163. DTBHN decomposes with a half-life time of 29 min. at 65 °C to give tert-butoxyl radicals and nitrogen. It is a stable solid, easily prepared from tert-butyl bromide and commercially available sodium hyponitrite (Aldrich): Mendenhall, G. D. Tetrahedron Lett. 1983, 24, 451. For further preparation details, see: Banks, J. T.; Scaiano, J. C.; Adam, W.; Oestrich, R. S. J. Am. Chem. Soc. 1993, 115, 2473. For a previous use of DTBHN to generate stannyl radicals, see: Dang, H. S.; Roberts, B. P. J. Chem. Soc., Perkin Trans. 1 1996, 769.
    • (1966) Tetrahedron Lett. , vol.49 , pp. 6163
    • Kiefer, H.1    Traylor, T.G.2
  • 20
    • 0242371428 scopus 로고
    • Kiefer, H.; Traylor, T. G. Tetrahedron Lett. 1966, 49, 6163. DTBHN decomposes with a half-life time of 29 min. at 65 °C to give tert-butoxyl radicals and nitrogen. It is a stable solid, easily prepared from tert-butyl bromide and commercially available sodium hyponitrite (Aldrich): Mendenhall, G. D. Tetrahedron Lett. 1983, 24, 451. For further preparation details, see: Banks, J. T.; Scaiano, J. C.; Adam, W.; Oestrich, R. S. J. Am. Chem. Soc. 1993, 115, 2473. For a previous use of DTBHN to generate stannyl radicals, see: Dang, H. S.; Roberts, B. P. J. Chem. Soc., Perkin Trans. 1 1996, 769.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 451
    • Mendenhall, G.D.1
  • 21
    • 0001518583 scopus 로고
    • Kiefer, H.; Traylor, T. G. Tetrahedron Lett. 1966, 49, 6163. DTBHN decomposes with a half-life time of 29 min. at 65 °C to give tert-butoxyl radicals and nitrogen. It is a stable solid, easily prepared from tert-butyl bromide and commercially available sodium hyponitrite (Aldrich): Mendenhall, G. D. Tetrahedron Lett. 1983, 24, 451. For further preparation details, see: Banks, J. T.; Scaiano, J. C.; Adam, W.; Oestrich, R. S. J. Am. Chem. Soc. 1993, 115, 2473. For a previous use of DTBHN to generate stannyl radicals, see: Dang, H. S.; Roberts, B. P. J. Chem. Soc., Perkin Trans. 1 1996, 769.
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  • 22
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    • Kiefer, H.; Traylor, T. G. Tetrahedron Lett. 1966, 49, 6163. DTBHN decomposes with a half-life time of 29 min. at 65 °C to give tert-butoxyl radicals and nitrogen. It is a stable solid, easily prepared from tert-butyl bromide and commercially available sodium hyponitrite (Aldrich): Mendenhall, G. D. Tetrahedron Lett. 1983, 24, 451. For further preparation details, see: Banks, J. T.; Scaiano, J. C.; Adam, W.; Oestrich, R. S. J. Am. Chem. Soc. 1993, 115, 2473. For a previous use of DTBHN to generate stannyl radicals, see: Dang, H. S.; Roberts, B. P. J. Chem. Soc., Perkin Trans. 1 1996, 769.
    • (1996) J. Chem. Soc., Perkin Trans. 1 , pp. 769
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    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 90
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