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Photoadditions of Silyl Butadienyl Ether to 1,2-Diketones

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참고문헌 (15)

  1. Cho, D. W., , J. Org. Chem, 73, pp.4539~ (2008)
  2. Yoon, U. C., , Bull. Korean Chem. Soc, 23, pp.1218~ (2002)
  3. Park, H. J., , J. Org. Chem, 77, pp.10304~ (2012)
  4. Otera, J., "H. ; Fukuzumi", J. Org. Chem, 57 (1992)
  5. Fukuzumi, S., , J. Am. Chem. Soc, 114, pp.10271~ (1992)
  6. Abe, M., , J. Chem. Soc. Perkin Trans 1, pp.3253~ (1998)
  7. Gream, G. E., , Tetrahedron Lett, 3479 (1970)
  8. Arnold, D. R., "Advances in Photochemistry" (1968), Interscience Publishers
  9. Gassman, P. G., , J. Org. Chem, 53, pp.1097~ (1988)
  10. Ito, Y., , J. Am. Chem. Soc, 97, pp.649~ (1975)
  11. Sun Wha Oh, "Single Electron Transfer Induced Photoaddition Reactions of Silyl Enol Ether to N-Methylphthalimide", Bulletin of the Korean Chemical Society, 28(4), pp.629~634 (2007), 대한화학회
  12. Audebert, P., , J. Electroanal. Chem, 445, pp.203~ (1998)
  13. "Structural assignment of 6 was made on the basis of NMR and HRMS spectroscopic data. 1H-NMR (CDCl3) 2.87 (q, 1H, J = 8.4 Hz), 3.04 (q, 1H, J = 8.0 Hz), 6.05 (q, 1H), 6.88 (q, 1H), 7.59−7.79 (m, 3H), 7.89−7.98 (m, 2H), 8.15 (d, 1H), 9.36 (d, 1H); 13C-NMR 41.1, 79.0, 120.7, 122.5, 125.7, 128.4, 128.7, 129.8, 130.5, 132.4, 136.1, 138.4, 140.9, 150.7, 193.5, 204.0; HRMS (EI) m", z 252.0788 (calc. C16H12O3, 252.0786)
  14. "NMR spectroscopic data of 7a and 7b are followed. 7a: 1H-NMR −0.21 (s, 9H), 2.22 (m, 1H), 2.77 (d, 1H), 5.79 (d, 1H), 6.08 (m, 1H), 6.19 (m, 1H), 7.56−8.16 (m, 6H); 13C-NMR −0.1, 30.1, 77.2, 89.7, 122.2, 123.6, 124.6, 125.0, 127.8, 128.3, 128.7, 130.5, 130.6, 132.1, 140.2, 141.5, 202.1. 7b: 1H-NMR −0.21 (s, 9H), 2.13 (d, 1H), 2.83 (m, 1H), 6.09 (d, 1H), 6.17-6.30 (m, 2H), 7.56−8.16 (m, 6H); 13C-NMR −0.1, 30.3, 77.4, 89.9, 122.1, 123.4, 124.7, 125.1, 127.7, 128.3, 128.8, 130.6, 130.7, 132.0, 140.3, 141.7, 202.2", ~
  15. "Photoproduct 9 and 10 were obtained as one of possible diastereomers", ~

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