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1
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1542502091
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-
For reviews on polycyclic ethers, see:
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For reviews on polycyclic ethers, see:. Yasumoto T., and Murata M. Chem. Rev. 93 (1993) 1897
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(1993)
Chem. Rev.
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, pp. 1897
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Yasumoto, T.1
Murata, M.2
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6
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0000563379
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-
For reviews on synthetic methods and total syntheses, see:
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For reviews on synthetic methods and total syntheses, see:. Alvarez E., Candenas M.-L., Pérez R., Ravelo J., and Martín J.D. Chem. Rev. 95 (1995) 1953
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Chem. Rev.
, vol.95
, pp. 1953
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Alvarez, E.1
Candenas, M.-L.2
Pérez, R.3
Ravelo, J.4
Martín, J.D.5
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24
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0141508988
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Kadota I., Takamura H., Sato K., Ohno A., Matsuda K., Satake M., and Yamamoto Y. J. Am. Chem. Soc. 125 (2003) 11893
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(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 11893
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-
Kadota, I.1
Takamura, H.2
Sato, K.3
Ohno, A.4
Matsuda, K.5
Satake, M.6
Yamamoto, Y.7
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25
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0035817276
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Nagumo Y., Oguri H., Shindo Y., Sasaki S., Oishi T., Hirama M., Tomioka Y., Mizugaki M., and Tsumuraya T. Bioorg. Med. Chem. Lett. 11 (2001) 2037
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(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2037
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Nagumo, Y.1
Oguri, H.2
Shindo, Y.3
Sasaki, S.4
Oishi, T.5
Hirama, M.6
Tomioka, Y.7
Mizugaki, M.8
Tsumuraya, T.9
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26
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7744246249
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Matsuo G., Kawamura K., Hori N., Matsukura H., and Nakata T. J. Am. Chem. Soc. 126 (2004) 14374
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(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 14374
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Matsuo, G.1
Kawamura, K.2
Hori, N.3
Matsukura, H.4
Nakata, T.5
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35
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33751439440
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note
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3): δ 169.8, 140.3, 137.0, 133.7, 129.2, 128.8, 128.3, 128.1, 126.1, 101.9, 76.6, 76.4, 75.5, 74.9, 73.5, 68.9, 68.8, 58.0, 34.6, 34.0, 21.0.
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36
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33751417030
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note
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3): δ 169.2, 139.9, 137.1, 133.8, 129.2, 129.0, 128.4, 128.2, 126.1, 101.8, 76.8, 76.7, 73.9, 73.7, 73.4, 70.3, 69.0, 58.0, 34.2, 33.7, 20.9.
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37
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33751422184
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note
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One enantiomer of the racemic alcohol 10 is drawn for simplicity.
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-
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40
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33751437889
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note
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3): δ 170.2, 140.5, 133.4, 128.9, 128.0, 77.7, 74.5, 70.5, 58.4, 34.9, 31.6, 29.8, 29.2, 24.9, 22.6, 21.1, 14.1.
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-
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41
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33751428565
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note
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3): δ 170.2, 140.5, 133.4, 128.9, 128.0, 77.7, 74.5, 70.4, 58.4, 34.9, 31.6, 29.8, 29.21, 29.16, 24.9, 22.6, 21.1, 14.1.
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-
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42
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33751397847
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note
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The other two products should be stereoisomers.
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43
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0037068182
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Satake M., Shoji M., Oshima Y., Naoki H., Fujita T., and Yasumoto T. Tetrahedron Lett. 43 (2002) 5829
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(2002)
Tetrahedron Lett.
, vol.43
, pp. 5829
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Satake, M.1
Shoji, M.2
Oshima, Y.3
Naoki, H.4
Fujita, T.5
Yasumoto, T.6
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44
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0037148014
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Cabianca E., Chéry F., Rollin P., Tatibouët A., and De Lucchi O. Tetrahedron Lett. 43 (2002) 585
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(2002)
Tetrahedron Lett.
, vol.43
, pp. 585
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Cabianca, E.1
Chéry, F.2
Rollin, P.3
Tatibouët, A.4
De Lucchi, O.5
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45
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33751417751
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note
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3): δ 170.3, 140.1, 133.5, 129.0, 128.0, 78.2, 73.2, 68.7, 58.9, 35.6, 31.6, 29.2, 27.8, 25.2, 24.9, 22.5, 21.0, 14.0.
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