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For a recent review see: (a) Ghosh, C. K.; Ghosh, C. Indian J. Chem. 1997, 968. For the first example of 3-acyl-4-pyrones functioning as dienophiles see: (b) Groundwater, P. W.; Hibbs, D. E.; Hursthouse, M. B.; Nyerges, M. J. Chem. Soc., Perkin Trans. 1 1997, 163.
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For a recent elegant study on 3-acyl- and 3-cyano-4-pyrones functioning as dienophiles see: Chen, D.; Wang, J.; Totah, N. I. J. Org. Chem. 1999, 64, 1776.
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For studies on 3-nitrile-4-benzopyrones functioning as dienophiles see: (a) Hsung, R. P. J. Org. Chem. 1997, 62, 7904. (b) Hsung, R. P. Heterocycles 1998, 48, 421. (c) Granum, K. G.; Merkel, G.; Mulder, J. A.; Debbins, S. A.; Hsung, R. P. Tetrahedron Lett. 1998, 9597.
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For studies on 3-nitrile-4-benzopyrones functioning as dienophiles see: (a) Hsung, R. P. J. Org. Chem. 1997, 62, 7904. (b) Hsung, R. P. Heterocycles 1998, 48, 421. (c) Granum, K. G.; Merkel, G.; Mulder, J. A.; Debbins, S. A.; Hsung, R. P. Tetrahedron Lett. 1998, 9597.
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For the only other examples of benzopyrones functioning as dienophiles see: (a) Cremins, P. J.; Saengchantara, S. T.; Wallace, T. W. Tetrahedron 1987, 13, 3075. (b) Ohkata, K.; Kubo, T.; Miyamoto, K.; Ono, M.; Yamamoto, J.; Akiba, K. Heterocycles 1994, 38, 1483.
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For studies related to arisugacin see: (a) Obata, R.; Sunazuka, T.; Tian, Z.; Tomoda, H.; Harigaya, Y.; Ömura, S.; Smith, A. B. III. Chem. Lett. 1997, 935. (b) Hua, D. H.; Chen, Y.; Sin, H.-S.; Maroto, M. J.; Robinson, P. D.; Newell, S. W.; Perchellet, E. M.; Ladesich, J. B.; Freeman, J. A.; Perchellet, J.-P.; Chiang, P. K. J. Org. Chem. 1997, 62, 6888.
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For our other related efforts see: (a) Hsung, R. P.; Shen, H. C.; Douglas, C. J.; Morgan, C. D.; Degen, S. J.; Yao, L. J. J. Org. Chem. 1999, 64, 690. (b) Hsung, R. P.; Wei, L.-L.; Sklenicka, H. M.; Douglas, C. J.; McLaughlin, M. J.; Mulder, J. A.; Yao, L. J. Org. Lett. 1999, 1, 509. (c) Wei, L.-L.; Xiong, H.; Douglas, C. J.; Hsung, R. P. Tetrahedron Lett. 1999, 6903. (d) Hsung, R. P.; Zificsak, C. A.; Wei, L.-L.; Douglas, C. J.; Xiong, H.; Mulder, J. A. Org. Lett. 1999, 1, 1237-1240. (e) Douglas, C. J.; Sklenicka, H. M.; Shen, H. C.; Mathias, D. S.; Golding, G. M.; Hsung, R. P.; Degen, S. J.; Morgan, C. D.; Mueller, K. L.; Seurer, L. M.; Shih, R. A. Tetrahedron 1999, 55, in press.
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Degen, S.J.5
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For our other related efforts see: (a) Hsung, R. P.; Shen, H. C.; Douglas, C. J.; Morgan, C. D.; Degen, S. J.; Yao, L. J. J. Org. Chem. 1999, 64, 690. (b) Hsung, R. P.; Wei, L.-L.; Sklenicka, H. M.; Douglas, C. J.; McLaughlin, M. J.; Mulder, J. A.; Yao, L. J. Org. Lett. 1999, 1, 509. (c) Wei, L.-L.; Xiong, H.; Douglas, C. J.; Hsung, R. P. Tetrahedron Lett. 1999, 6903. (d) Hsung, R. P.; Zificsak, C. A.; Wei, L.-L.; Douglas, C. J.; Xiong, H.; Mulder, J. A. Org. Lett. 1999, 1, 1237-1240. (e) Douglas, C. J.; Sklenicka, H. M.; Shen, H. C.; Mathias, D. S.; Golding, G. M.; Hsung, R. P.; Degen, S. J.; Morgan, C. D.; Mueller, K. L.; Seurer, L. M.; Shih, R. A. Tetrahedron 1999, 55, in press.
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Mulder, J.A.6
Yao, L.7
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14
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0033578602
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For our other related efforts see: (a) Hsung, R. P.; Shen, H. C.; Douglas, C. J.; Morgan, C. D.; Degen, S. J.; Yao, L. J. J. Org. Chem. 1999, 64, 690. (b) Hsung, R. P.; Wei, L.-L.; Sklenicka, H. M.; Douglas, C. J.; McLaughlin, M. J.; Mulder, J. A.; Yao, L. J. Org. Lett. 1999, 1, 509. (c) Wei, L.-L.; Xiong, H.; Douglas, C. J.; Hsung, R. P. Tetrahedron Lett. 1999, 6903. (d) Hsung, R. P.; Zificsak, C. A.; Wei, L.-L.; Douglas, C. J.; Xiong, H.; Mulder, J. A. Org. Lett. 1999, 1, 1237-1240. (e) Douglas, C. J.; Sklenicka, H. M.; Shen, H. C.; Mathias, D. S.; Golding, G. M.; Hsung, R. P.; Degen, S. J.; Morgan, C. D.; Mueller, K. L.; Seurer, L. M.; Shih, R. A. Tetrahedron 1999, 55, in press.
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0001541454
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For our other related efforts see: (a) Hsung, R. P.; Shen, H. C.; Douglas, C. J.; Morgan, C. D.; Degen, S. J.; Yao, L. J. J. Org. Chem. 1999, 64, 690. (b) Hsung, R. P.; Wei, L.-L.; Sklenicka, H. M.; Douglas, C. J.; McLaughlin, M. J.; Mulder, J. A.; Yao, L. J. Org. Lett. 1999, 1, 509. (c) Wei, L.-L.; Xiong, H.; Douglas, C. J.; Hsung, R. P. Tetrahedron Lett. 1999, 6903. (d) Hsung, R. P.; Zificsak, C. A.; Wei, L.-L.; Douglas, C. J.; Xiong, H.; Mulder, J. A. Org. Lett. 1999, 1, 1237-1240. (e) Douglas, C. J.; Sklenicka, H. M.; Shen, H. C.; Mathias, D. S.; Golding, G. M.; Hsung, R. P.; Degen, S. J.; Morgan, C. D.; Mueller, K. L.; Seurer, L. M.; Shih, R. A. Tetrahedron 1999, 55, in press.
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Mulder, J.A.6
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in press
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For our other related efforts see: (a) Hsung, R. P.; Shen, H. C.; Douglas, C. J.; Morgan, C. D.; Degen, S. J.; Yao, L. J. J. Org. Chem. 1999, 64, 690. (b) Hsung, R. P.; Wei, L.-L.; Sklenicka, H. M.; Douglas, C. J.; McLaughlin, M. J.; Mulder, J. A.; Yao, L. J. Org. Lett. 1999, 1, 509. (c) Wei, L.-L.; Xiong, H.; Douglas, C. J.; Hsung, R. P. Tetrahedron Lett. 1999, 6903. (d) Hsung, R. P.; Zificsak, C. A.; Wei, L.-L.; Douglas, C. J.; Xiong, H.; Mulder, J. A. Org. Lett. 1999, 1, 1237-1240. (e) Douglas, C. J.; Sklenicka, H. M.; Shen, H. C.; Mathias, D. S.; Golding, G. M.; Hsung, R. P.; Degen, S. J.; Morgan, C. D.; Mueller, K. L.; Seurer, L. M.; Shih, R. A. Tetrahedron 1999, 55, in press.
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Degen, S.J.7
Morgan, C.D.8
Mueller, K.L.9
Seurer, L.M.10
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For some examples see: (a) Grinberg, L. N.; Newmark, H.; Kitrossky, N.; Rahamim, E.; Chevion, M.; Rachmilewitz, E. A. Biochem. Pharmacol. 1997, 54, 973. (b) Leanderson, P.; Faresjö, A. O.; Tagesson, C. Free Radical Biol. Med. 1997, 23, 235. (c) Agullo, G.; Payrastre, L. G.; Manenti, S.; Viala, C.; Résmésy, C.; Chap, H.; Payraste, B. Biochem. Pharmacol. 1997, 53, 1649. (d) Fotsis, T.; Pepper, M. S.; Aktas, E.; Breit, S.; Rasku, S.; Adlercreutz, H.; Wähälä, K.; Montesano, R.; Scheweigerer, L. Cancer Res. 1997, 57, 2916. (e) Wright, J. S.; Carpenter, D. J.; McKay, D. J.; Ingold, K. U. J. Am. Chem. Soc. 1997, 119, 4245.
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These O-methyl oximes were not very stable under basic conditions
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These O-methyl oximes were not very stable under basic conditions.
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