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Isaka, M.1
Rugseree, N.2
Maithip, P.3
Kongsaeree, P.4
Prabpai, S.5
Thebtaranonth, Y.6
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3
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64549113865
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Jpn. Kokai Tokkyo Koho, JP 2001247574
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Koizumi, F; Hasegawa, A.; Ando, K.; Ogawa, T.; Hara, M. Jpn. Kokai Tokkyo Koho 2001, JP 2001247574.
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Koizumi, F.1
Hasegawa, A.2
Ando, K.3
Ogawa, T.4
Hara, M.5
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4
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0037170152
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He H., Yang H.Y., Bigelis R., Solum E.H., Greenstein M., and Carter G.Y. Tetrahedron Lett. 43 (2002) 1633-1636
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(2002)
Tetrahedron Lett.
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He, H.1
Yang, H.Y.2
Bigelis, R.3
Solum, E.H.4
Greenstein, M.5
Carter, G.Y.6
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5
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55549118879
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Shiono Y., Shimanuki K., Hiramatsu F., Koseki T., Tetsuya M., Fujisawa N., and Kimura K. Bioorg. Med. Chem. Lett. 18 (2008) 6050-6053
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Shiono, Y.1
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Tetsuya, M.5
Fujisawa, N.6
Kimura, K.7
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10
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60849120481
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When this manuscript is in preparation, an elegant synthesis of the decahydrofluorene core of the hirsutellones is reported:
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When this manuscript is in preparation, an elegant synthesis of the decahydrofluorene core of the hirsutellones is reported:. Tilley S.D., Reber K.P., and Sorensen E.J. Org. Lett. 11 (2009) 701-703
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(2009)
Org. Lett.
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Tilley, S.D.1
Reber, K.P.2
Sorensen, E.J.3
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13
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36749072063
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Gupta S., Rajagopalan M., Alhamadsheh M.M., Tillekeratne L.M.V., and Hudson R.A. Synthesis (2007) 3512-3518
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(2007)
Synthesis
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Gupta, S.1
Rajagopalan, M.2
Alhamadsheh, M.M.3
Tillekeratne, L.M.V.4
Hudson, R.A.5
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14
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64549132320
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note
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A seven-step sequence was followed to prepare 12:{A figure is presented}.
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15
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64549101803
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A routine synthetic sequence was followed to afford 17: {A figure is presented}.
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A routine synthetic sequence was followed to afford 17: {A figure is presented}.
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16
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0037956005
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For selective deprotection of phenolic TBS ether, see:
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For selective deprotection of phenolic TBS ether, see:. Ankala S.V., and Fenteany G. Synlett (2003) 825-828
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(2003)
Synlett
, pp. 825-828
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Ankala, S.V.1
Fenteany, G.2
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23
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33746289007
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Tsuchikawa H., Matsushita N., Matsumori N., Murata M., and Oishi T. Tetrahedron Lett. 47 (2006) 6187-6191
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(2006)
Tetrahedron Lett.
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Tsuchikawa, H.1
Matsushita, N.2
Matsumori, N.3
Murata, M.4
Oishi, T.5
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25
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3242683644
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For an example, see:
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For an example, see:. Cook G.R., and Sun L. Org. Lett. 6 (2004) 2481-2484
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(2004)
Org. Lett.
, vol.6
, pp. 2481-2484
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Cook, G.R.1
Sun, L.2
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27
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64549116541
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note
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+ 592.3434, found 592.3445.
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28
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32044445556
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Suzuki T., Tanaka N., Matsumura T., Hosoya Y., and Nakada M. Tetrahedron Lett. 47 (2006) 1593-1598
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(2006)
Tetrahedron Lett.
, vol.47
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Suzuki, T.1
Tanaka, N.2
Matsumura, T.3
Hosoya, Y.4
Nakada, M.5
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29
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33750437727
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Asano M., Inoue M., Watanabe K., Abe H., and Katoh T. J. Org. Chem. 71 (2006) 6942-6951
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J. Org. Chem.
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Asano, M.1
Inoue, M.2
Watanabe, K.3
Abe, H.4
Katoh, T.5
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30
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0023043811
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Houk's modeling on conformational preferenes of allylic groups in transition structures does not account for our result, see:
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Houk's modeling on conformational preferenes of allylic groups in transition structures does not account for our result, see:. Houk K.N., Paddon-Row M.N., Rondan N.G., Wu Y., Brown F.K., Spellmeyer D.C., Metz J.T., Li Y., and Loncharich R.J. Science 231 (1986) 1108-1117
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(1986)
Science
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Houk, K.N.1
Paddon-Row, M.N.2
Rondan, N.G.3
Wu, Y.4
Brown, F.K.5
Spellmeyer, D.C.6
Metz, J.T.7
Li, Y.8
Loncharich, R.J.9
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31
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12944325309
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For the examples of similar IMDA reactions consistent with Houk's modeling, see:
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For the examples of similar IMDA reactions consistent with Houk's modeling, see:. Jarosz S., Boryczko B., Cmoch P., Gomez A.M., and Lopez C. Tetrahedron: Asymmetry 16 (2005) 513-518
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(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 513-518
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Jarosz, S.1
Boryczko, B.2
Cmoch, P.3
Gomez, A.M.4
Lopez, C.5
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