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37049105803
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Tandem Michael addition/cyclization sequences have been reported separately for the synthesis of 4-oxy-type arylnaphthofuranone lignans: A. Pelter, R. S. Ward, P. Satyanarayana, and P. Collins, J. Chem. Soc., Perkin Trans. 1, 1983, 643;
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37049072096
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A. Pelter, R. S. Ward, M. C. Pritchard, and I. T. Kay, J. Chem. Soc., Perkin Trans. 1, 1988, 1603;
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37049103805
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For other syntheses: H. P. Plaumann, J. G. Smith, and R. Rodorigo, J. Chem. Soc., Chem. Commun., 1980, 354;
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12
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37049083667
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For recent synthetic approaches to other types of arylnaphthofuranone lignans, see: K. Kobayashi, Y. Kanno, S. Seko, and H. Suginome, J. Chem. Soc., Perkin Trans. 1, 1992, 3111;
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Kobayashi, K.1
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T. Hattori, H. Tanaka, Y. Okaishi, and S. Miyano, J. Chem. Soc., Perkin Trans. 1, 1995, 235;
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33748976541
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Y. Tanabe, S. Seko, Y. Nishii, T. Yoshida, N. Utsumi, and G. Suzukamo, J. Chem. Soc., Perkin Trans. 1, 1996, 2157.
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0004266767
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Cambridge Univ. Press, Cambridge
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See also: C. D. Ayres and J. D. Loike, 'Lignans,' Cambridge Univ. Press, Cambridge, 1990;
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Lignans
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Ayres, C.D.1
Loike, J.D.2
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0029278712
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and references cited therein
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R. S. Ward, Nat. Prod. Rep., 1995, 12, 183 and references cited therein.
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Ward, R.S.1
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21
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18844455024
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The use of one equivalent of LDA gave a somewhat lower yield than the use of 2 equivalents
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The use of one equivalent of LDA gave a somewhat lower yield than the use of 2 equivalents.
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22
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18844406505
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L. H. Klemn, D. H. Lee, K. W. Gopinath, and C. E. Klopfenstein, J. Org. Chem. 1966, 31, 2376.
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L. H. Klemn, K. W. Gopinath, D. H. Lee, and F. W. Kelly, Tetrahedron, 1966, 22, 1797.
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M. Okigawa, T. Maeda, and N. Kawanoe, Tetrahedron, 1970, 26, 4301;
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S. Ghosal, P. S. Ramaballav, and R. S. Srivastava, Phytochemistry, 1974, 13, 1933.
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