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1
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(a) Takahashi, H.; Osada, H.; Koshino, H.; Kudo, T.; Amano, S.; Shimizu, S.; Yoshihama, M.; Isono, K. J. Antibiot. 1992, 45, 1409-1413.
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Yoshihama, M.7
Isono, K.8
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2
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0026756077
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(b) Takahashi, H.; Osada, H.; Koshino, H.; Sasaki, M.; Onose, R.; Nakakoshi, M.; Yoshihama, M.; Isono, K. J. Antibiot. 1992, 45, 1414-1419.
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Takahashi, H.1
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Yoshihama, M.7
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0026764947
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Koshino, H.1
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4
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0027979020
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5
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0030576964
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Shimizu, T.; Kobayashi, R.; Osako, K.; Nakata, T. Tetrahedron Lett. 1996, 37, 6755-6758.
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Shimizu, T.1
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8
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85034141626
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note
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β-Elimination of the silylated C-5 hydroxy group occurred under various basic conditions.
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9
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85034120525
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note
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The mono(allyl succinate) 6 was prepared by alcoholysis of succinic anhydride with allyl alcohol in 94% yield.
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10
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85034152026
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note
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During evaporation of the solvents, the resulting diol 12 was converted into the THP derivative, which was then treated with TsOH in MeOH to give 12.
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11
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2542433188
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Carlsen, P. H. J.; Katsuki, T.; Martin, V. S.; Sharpless, K. B. J. Org. Chem. 1981, 46, 3936-3938.
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Carlsen, P.H.J.1
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12
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0030903859
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Shimizu, T.; Osako, K.; Nakata, T. Tetrahedron Lett. 1997, 38, 2685-2688.
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Shimizu, T.1
Osako, K.2
Nakata, T.3
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13
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85034145372
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note
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Treatment of 15 with TBSOTf exclusively gave the lactone 14.
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17
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0001667321
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3, 90°C (90%). (a) Otera, J.; Yano, T.; Kawabata, A.; Nozaki, H. Tetrahedron Lett. 1986, 27, 2383-2386.
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33751500481
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0002497114
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20
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0012016624
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0032563845
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22
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0001624845
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(a) Baudin, J. B.; Hareau, G.; Julia, S. A.; Ruel, O. Bull. Soc. Chim. Fr. 1993, 130, 336-357.
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23
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0000355152
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(b) Baudin, J. B.; Hareau, G.; Julia, S. A.; Lorne, R.; Ruel, O. Bull. Soc. Chim. Fr. 1993, 130, 856-878.
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24
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0029933368
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Application to total synthesis: (c) Bellingham, R.; Jarowicki, K.; Kocienski, P.; Martin, V. Synthesis 1996, 285-296.
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Bellingham, R.1
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Martin, V.4
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