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3
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0000084592
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Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds), Pergamon Press
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In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprehensive Heterocyclic Chemistry II Vol. 2 (1996), Pergamon Press 259
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4
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Katritzky A.R., and Rees C.W. (Eds), Pergamon Press
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In: Katritzky A.R., and Rees C.W. (Eds). Comprehensive Heterocyclic Chemistry Vol. 4 (1984), Pergamon Press 531
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6
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0001594744
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For the isolation of shoreaphenol, see:
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For the isolation of shoreaphenol, see:. Saraswathy A., Purushothaman K.K., Patra A., Dey A.K., and Kundu A.B. Phytochemistry 31 (1992) 2561
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Saraswathy, A.1
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Patra, A.3
Dey, A.K.4
Kundu, A.B.5
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7
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0034956715
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For the isolation of hopeafuran, see:
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For the isolation of hopeafuran, see:. Tanaka T., Ito T., Ido Y., Nakaya K., Iinuma M., and Chelladurai V. Chem. Pharm. Bull. 49 (2001) 785
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Tanaka, T.1
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Nakaya, K.4
Iinuma, M.5
Chelladurai, V.6
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8
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0035189827
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For the isolation of iantheran A, see:
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For the isolation of iantheran A, see:. Okamoto Y., Ojika M., Suzuki S., Murakami M., and Sakagami Y. Bioorg. Med. Chem. 9 (2001) 179
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Okamoto, Y.1
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Suzuki, S.3
Murakami, M.4
Sakagami, Y.5
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10
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36148961568
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For the isolation and biological studyof other iantherans, see:
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For the isolation and biological studyof other iantherans, see:. Greve H., Meis S., Kassack M.U., Kehraus S., Krick A., Wright A.D., and König G.M. J. Med. Chem. 50 (2007) 5600
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Wright, A.D.6
König, G.M.7
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11
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43949112301
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For selected examples, see:
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For selected examples, see:. Rizzo S., Riviere C., Piazzi L., Bisi A., Gobbi S., Bartolini M., Andrisano V., Morroni F., Tarozzi A., Monti J.-F., and Rampa A. J. Med. Chem. 51 (2008) 2883
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Bartolini, M.6
Andrisano, V.7
Morroni, F.8
Tarozzi, A.9
Monti, J.-F.10
Rampa, A.11
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38949201262
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Kirilmis C., Ahmedzade M., Servi S., Koca M., Kizirgil A., and Kazaz C. Eur. J. Med. Chem. 43 (2008) 300
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Kirilmis, C.1
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Kizirgil, A.5
Kazaz, C.6
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13
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34250186811
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Filzen G.F., Bratton L., Cheng X.-M., Erasga N., Geyer A., Lee C., Lu G., Pulaski J., Sorenson R.J., Unangst P.C., Trivedi B.K., and Xu X. Bioorg. Med. Chem. Lett. 17 (2007) 3630
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Filzen, G.F.1
Bratton, L.2
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Geyer, A.5
Lee, C.6
Lu, G.7
Pulaski, J.8
Sorenson, R.J.9
Unangst, P.C.10
Trivedi, B.K.11
Xu, X.12
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14
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38149041459
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Salih K.S.M., Ayoub M.T., Saadeh H.A., Al-Masoudi N.A., and Mubarak M.S. Heterocycles 717 (2007) 1577
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Salih, K.S.M.1
Ayoub, M.T.2
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Al-Masoudi, N.A.4
Mubarak, M.S.5
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15
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33845291522
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Dixit M., Tripathi B.K., Tamrakar A.K., Srivastava A.K., Kumar B., and Goel A. Bioorg. Med. Chem. 15 (2007) 727
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Dixit, M.1
Tripathi, B.K.2
Tamrakar, A.K.3
Srivastava, A.K.4
Kumar, B.5
Goel, A.6
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16
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44449160072
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For recent examples, see:
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For recent examples, see:. Huang X.-C., Liu Y.-L., Liang Y., Pi S.-F., Wang F., and Li J.-H. Org. Lett. 10 (2008) 1525
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(2008)
Org. Lett.
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Huang, X.-C.1
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Wang, F.5
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28244470363
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Lu K., Luo T., Xiang Z., You Z., Fathi R., Chen J., and Yang Z. J. Comb. Chem. 7 (2005) 958
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Lu, K.1
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You, Z.4
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22
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0043227327
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Nicolaou K.C., Snyder S.A., Bigot A., and Pfefferkorn J. Angew. Chem., Int. Ed. 39 (2000) 1093
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Nicolaou, K.C.1
Snyder, S.A.2
Bigot, A.3
Pfefferkorn, J.4
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24
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0032858829
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3 was used to make benzofurans via demethylation and cyclodehydration, only four examples are shown and the yields are low.
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3 was used to make benzofurans via demethylation and cyclodehydration, only four examples are shown and the yields are low. Dupont R., and Cotelle P. Synthesis (1999) 1651
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(1999)
Synthesis
, pp. 1651
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Dupont, R.1
Cotelle, P.2
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25
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53149151117
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note
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4, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to give the benzofuran or naphthofuran 5.
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26
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53149097037
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note
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Spectral data:
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27
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53149151919
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note
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3 led to the only demethylated product 5e′.{A figure is presented}
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29
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30344457020
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For other synthesis and biological evaluation of 5i as a novel anticancer agent, see:
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For other synthesis and biological evaluation of 5i as a novel anticancer agent, see:. Srivastava V., Negi A.S., Kumar J.K., Faridi U., Sisodia B.S., Darokar M.P., Luqman S., and Khanuja S.P.S. Bioorg. Med. Chem. Lett. 16 (2006) 911
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Bioorg. Med. Chem. Lett.
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Srivastava, V.1
Negi, A.S.2
Kumar, J.K.3
Faridi, U.4
Sisodia, B.S.5
Darokar, M.P.6
Luqman, S.7
Khanuja, S.P.S.8
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30
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53149132056
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note
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3, which is believed to be consumed as a consequence of the coordination to the ester moiety in 4p.
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31
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53149148966
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note
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CCDC 694499 contains the supplementary crystallographic data for compound 5p. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
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