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Orjala, J.1
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Erdelmeier, C.A.J.3
Sticher, O.4
Rali, T.5
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2
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0029067548
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Mimaki Y., Kameyama A., Sashida Y., Miyata Y., and Fujii A. Chem. Pharm. Bull. 43 (1995) 893
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Mimaki, Y.1
Kameyama, A.2
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Fujii, A.5
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3
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23344441452
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Synthesis of (±)-3:
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Synthesis of (±)-3:. Yamashita M., Inaba T., Nagahama M., Shimizu T., Kosaka S., Kawasaki I., and Ohta S. Org. Biomol. Chem. 3 (2005) 2296
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Yamashita, M.1
Inaba, T.2
Nagahama, M.3
Shimizu, T.4
Kosaka, S.5
Kawasaki, I.6
Ohta, S.7
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4
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31344432126
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Yamashita M., Shimizu T., Inaba T., Takada A., Takao I., Kawasaki I., and Ohta S. Heterocycles 65 (2005) 1099
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Shimizu, T.2
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Takada, A.4
Takao, I.5
Kawasaki, I.6
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5
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34447273377
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Yamashita M., Inaba T., Shimizu T., Kawasaki I., and Ohta S. Synlett (2004) 1987
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6
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Matuura, Y.5
Kawasaki, I.6
Tanaka, T.7
Maezaki, N.8
Ohta, S.9
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9
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Kawada, A.1
Mitamura, S.2
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13
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34447273380
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note
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4.
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14
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0030873950
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Sen E.S., Roach L.S., Bogg K.J., Ewing J.G., and Magrath J. J. Org. Chem. 62 (1997) 6684
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Sen, E.S.1
Roach, L.S.2
Bogg, K.J.3
Ewing, J.G.4
Magrath, J.5
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15
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34447249830
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note
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3. Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 650339 for 10. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [Fax: +44 (0) 1223 336033; E-mail: deposit@ccdc.cam.ac.uk].
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16
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34447273378
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note
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5: C, 73.56; H, 7.60. Found: C, 73.32; H, 7.56.
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17
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34447273379
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note
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3.
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18
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34447264553
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note
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We requested the spectral data of adunctin E (1) from Dr. Sticher, but to date we have not received any information in this regard.
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19
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34447249829
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note
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Linderol A (3) was hydrogenated to afford dihydrolinderol A, a 6-epimer of 2. The spectral data for this compound were not consistent with those of 2. See Ref. 3b. We also prepared the possible compounds of which 3-phenylpropionyl group was substituted at the 2-position not the 4-position, and its 6-epimer, however, their spectral data were not consistent with those of 2.
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