-
1
-
-
42049089524
-
-
Huang, Z.; Cai, X.; Shao, C.; She, Z.; Xia, X.; Chen, Y.; Yang, J.; Zhou, S.; Lin, Y. Phytochemistry 2008, 69, 1604-1608
-
(2008)
Phytochemistry
, vol.69
, pp. 1604-1608
-
-
Huang, Z.1
Cai, X.2
Shao, C.3
She, Z.4
Xia, X.5
Chen, Y.6
Yang, J.7
Zhou, S.8
Lin, Y.9
-
3
-
-
0000921499
-
-
Shipchandler, M. T., and references cited therein
-
Shipchandler, M. T. Heterocycles 1975, 3, 471-520 and references cited therein
-
(1975)
Heterocycles
, vol.3
, pp. 471-520
-
-
-
4
-
-
0011387450
-
-
Raduranin A
-
Raduranin A: Asakawa, Y.; Toyota, M.; Takemoto, T. Phytochemistry 1978, 17, 2005-2010
-
(1978)
Phytochemistry
, vol.17
, pp. 2005-2010
-
-
Asakawa, Y.1
Toyota, M.2
Takemoto, T.3
-
6
-
-
27844513814
-
-
Halogenated derivatives of helianane
-
Halogenated derivatives of helianane: Martín, M. J.; Berrué, F.; Amade, P.; Fernández, R.; Francesch, A.; Reyes, F.; Cuevas, C. J. Nat. Prod. 2005, 68, 1554-1555
-
(2005)
J. Nat. Prod.
, vol.68
, pp. 1554-1555
-
-
Martín, M.J.1
Berrué, F.2
Amade, P.3
Fernández, R.4
Francesch, A.5
Reyes, F.6
Cuevas, C.7
-
7
-
-
79952488127
-
-
Izuchi, Y.; Kanomata, N.; Koshino, H.; Hongo, Y.; Nakata, T.; Takahashi, S. Tetrahedron: Asymmetry 2011, 22, 246-251
-
(2011)
Tetrahedron: Asymmetry
, vol.22
, pp. 246-251
-
-
Izuchi, Y.1
Kanomata, N.2
Koshino, H.3
Hongo, Y.4
Nakata, T.5
Takahashi, S.6
-
8
-
-
70350625335
-
-
Ye, Y.-Q.; Koshino, H.; Onose, J.; Yoshikawa, K.; Abe, N.; Takahashi, S. Org. Lett. 2009, 11, 5074-5077
-
(2009)
Org. Lett.
, vol.11
, pp. 5074-5077
-
-
Ye, Y.-Q.1
Koshino, H.2
Onose, J.3
Yoshikawa, K.4
Abe, N.5
Takahashi, S.6
-
9
-
-
70349160765
-
-
Takahashi, S.; Takahashi, R.; Hongo, Y.; Koshino, H.; Yamaguchi, K.; Miyagi, T. J. Org. Chem. 2009, 74, 6382-6385
-
(2009)
J. Org. Chem.
, vol.74
, pp. 6382-6385
-
-
Takahashi, S.1
Takahashi, R.2
Hongo, Y.3
Koshino, H.4
Yamaguchi, K.5
Miyagi, T.6
-
10
-
-
65549170594
-
-
Nishii, Y.; Higa, T.; Takahashi, S.; Nakata, T. Tetrahedron Lett. 2009, 50, 3597-3601
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 3597-3601
-
-
Nishii, Y.1
Higa, T.2
Takahashi, S.3
Nakata, T.4
-
11
-
-
79959769864
-
-
2 elimination as a side product. See
-
2 elimination as a side product. See
-
-
-
-
12
-
-
0344298502
-
-
Illuminati, G; Mandolini, L; Masci, B. J. Org. Chem. 1974, 39, 2598-2600
-
(1974)
J. Org. Chem.
, vol.39
, pp. 2598-2600
-
-
Illuminati, G.1
Mandolini, L.2
Masci, B.3
-
15
-
-
0000927905
-
-
Synthesis of (±)-helianane with a 8-membered ring via olefin metathesis was reported. See: Stefinovic, M.; Snieckus, V.
-
Synthesis of (±)-helianane with a 8-membered ring via olefin metathesis was reported. See: Stefinovic, M.; Snieckus, V. J. Org. Chem. 1998, 63, 2808-2809
-
(1998)
J. Org. Chem.
, vol.63
, pp. 2808-2809
-
-
-
18
-
-
0024523267
-
-
Watanabe, M.; Date, M.; Furukawa, S. Chem. Pharm. Bull. 1989, 37, 292-297
-
(1989)
Chem. Pharm. Bull.
, vol.37
, pp. 292-297
-
-
Watanabe, M.1
Date, M.2
Furukawa, S.3
-
19
-
-
0037012818
-
-
Kim, S.; Fan, G.-J.; Lee, J.; Lee, J. J.; Kim, D. J. Org. Chem. 2002, 67, 3127-3130
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3127-3130
-
-
Kim, S.1
Fan, G.-J.2
Lee, J.3
Lee, J.J.4
Kim, D.5
-
20
-
-
0038034726
-
-
Bauta, W. E.; Lovett, D. P.; Cantrell, W. R.; Burke, B. D. J. Org. Chem. 2003, 68, 5967-5973
-
(2003)
J. Org. Chem.
, vol.68
, pp. 5967-5973
-
-
Bauta, W.E.1
Lovett, D.P.2
Cantrell, W.R.3
Burke, B.D.4
-
21
-
-
79959748611
-
-
3. (11)
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3. (11)
-
-
-
-
22
-
-
34250204486
-
-
Takahashi, S.; Satoh, H.; Hongo, Y.; Koshino, H. J. Org. Chem. 2007, 72, 4578-4581
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4578-4581
-
-
Takahashi, S.1
Satoh, H.2
Hongo, Y.3
Koshino, H.4
-
23
-
-
79959750967
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For the structures of open-chain and cyclic dimers and their structural determination, see Supporting Information.
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For the structures of open-chain and cyclic dimers and their structural determination, see Supporting Information.
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-
-
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24
-
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79959767465
-
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Grubbs-Hoveyda catalysts first and second generation were also employed for the metathesis. However, the desired product was obtained in a low yield (4-10%).
-
Grubbs-Hoveyda catalysts first and second generation were also employed for the metathesis. However, the desired product was obtained in a low yield (4-10%).
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-
-
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25
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79959757287
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-
See Supporting Information.
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See Supporting Information.
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26
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8644242110
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-
Xu, Q.; Wang, J.; Huang, Y.; Zheng, Z.; Song, S.; Zhang, Y.; Su, W. Acta Oceanolog. Sin. 2004, 23, 541-547
-
(2004)
Acta Oceanolog. Sin.
, vol.23
, pp. 541-547
-
-
Xu, Q.1
Wang, J.2
Huang, Y.3
Zheng, Z.4
Song, S.5
Zhang, Y.6
Su, W.7
-
27
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79959715018
-
-
D value was denoted.
-
D value was denoted.
-
-
-
-
28
-
-
79959752328
-
-
Its absolute configuration is not shown.
-
Its absolute configuration is not shown.
-
-
-
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29
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72249119460
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-
Huang, Z.; Guo, Z.; Yang, R.; Yin, X.; Li, X.; Luo, W.; She, Z.; Lin, Y. Chem. Nat. Compd. 2009, 45, 625-628
-
(2009)
Chem. Nat. Compd.
, vol.45
, pp. 625-628
-
-
Huang, Z.1
Guo, Z.2
Yang, R.3
Yin, X.4
Li, X.5
Luo, W.6
She, Z.7
Lin, Y.8
-
30
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71749090849
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-
In this paper, the erroneous name "dothiorelone B" is used for dothiorelone A
-
Xu, J.; Kjer, J.; Sendker, J.; Wray, V.; Guan, H.; Edrada, R.; Mueller, W. E. G.; Bayer, M.; Lin, W.; Wu, J.; Proksch, P. Bioorg. Med. Chem. 2009, 17, 7362-7367. In this paper, the erroneous name "dothiorelone B" is used for dothiorelone A
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 7362-7367
-
-
Xu, J.1
Kjer, J.2
Sendker, J.3
Wray, V.4
Guan, H.5
Edrada, R.6
Mueller, W.E.G.7
Bayer, M.8
Lin, W.9
Wu, J.10
Proksch, P.11
-
31
-
-
76949103410
-
-
Abreu, L. M.; Phipps, R. K.; Pfenning, L. H.; Gotfredsen, C. H.; Takahashi, J. A.; Larsen, T. O. Tetrahedron Lett. 2010, 51, 1803-1805
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 1803-1805
-
-
Abreu, L.M.1
Phipps, R.K.2
Pfenning, L.H.3
Gotfredsen, C.H.4
Takahashi, J.A.5
Larsen, T.O.6
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32
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79959736923
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6 are summarized in Tables 2S and 3S; see Supporting Information.
-
6 are summarized in Tables 2S and 3S; see Supporting Information.
-
-
-
-
33
-
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79959722989
-
-
D of both natural products was reported to be negative although there was a discrepancy with their magnitude between refs 1 and 19.
-
D of both natural products was reported to be negative although there was a discrepancy with their magnitude between refs 1 and 19.
-
-
-
-
34
-
-
0024455346
-
-
Laughton, C. A.; Bradshaw, T. D.; Gescher, A. Int. J. Cancer 1989, 44, 320-324
-
(1989)
Int. J. Cancer
, vol.44
, pp. 320-324
-
-
Laughton, C.A.1
Bradshaw, T.D.2
Gescher, A.3
-
36
-
-
76949095154
-
-
Reddy, G. V.; Kumar, R. S. C.; Sreedhar, E.; Babu, K. S.; Rao, J. M. Tetrahedron Lett. 2010, 51, 1723-1726
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 1723-1726
-
-
Reddy, G.V.1
Kumar, R.S.C.2
Sreedhar, E.3
Babu, K.S.4
Rao, J.M.5
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