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Mori, T.1
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0021999512
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b) K. Takahashi, M. Kawabata, D. Uemura, Tetrahedron Lett. 1985, 26, 1077-1078.
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3
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33645084821
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For a review, see
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For a review, see M. G. Moloney, P. C. Trippier, M. Yaqoob, A. Wang, Curr. Drug Discovery Technol. 2004, 1, 181-199.
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Moloney, M.G.1
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4
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33847080428
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a) T. J. Donohoe, J. Y. K. Chiu, R. E. Thomas, Org. Lett. 2007, 9, 421-424;
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Donohoe, T.J.1
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5
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34249010472
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and references therein
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N. J. Bennet, J. C. Prodger, G. Pattenden, Tetrahedron 2007, 63, 6216-6231, and references therein.
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Bennet, N.J.1
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6
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0000919097
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A. S. Kende, K. Kawamura, R. J. DeVita, J. Am. Chem. Soc. 1990, 112, 4070-4072.
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Kende, A.S.1
Kawamura, K.2
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9
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33845375686
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a) H. Jin, J. Uenishi, W. J. Christ, Y. Kishi, J. Am. Chem. Soc. 1986, 108, 5644-5646;
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Jin, H.1
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10
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0000959935
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b) K. Takai, M. Tagashira, T. Kuroda, K. Oshima, K. Utimoto, H. Nozaki, J. Am. Chem. Soc. 1986, 108, 6048-6050.
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Takai, K.1
Tagashira, M.2
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Nozaki, H.6
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11
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0001539570
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For a review, see, Eds, Z. Rappoport, Y. Apeloig, Wiley, New York
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For a review, see I. Ojima, Z. Li, J. Zhu in The Chemistry of Organic Silicon Compounds, Vol. 2 (Eds.: Z. Rappoport, Y. Apeloig), Wiley, New York, 1998, pp. 1687-1792.
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Ojima, I.1
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12
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0001237287
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Tamao, K.1
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14
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10544224990
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A. Abiko, O. Moriya, S. A. Filla, S. Masamune, Angew. Chem. 1995, 107 869-871;
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Abiko, A.1
Moriya, O.2
Filla, S.A.3
Masamune, S.4
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17
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34548607722
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3 (1 equiv) in EtOH at room temperature, the corresponding Z isomer was obtained exclusively in 50% yield.
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3 (1 equiv) in EtOH at room temperature, the corresponding Z isomer was obtained exclusively in 50% yield.
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19
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0037015424
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X. Liu, J. R. Deschamp, J. M. Cook, Org. Lett. 2002, 4, 3339-3342.
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Liu, X.1
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20
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34548657678
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2O (3:1), which was the same solvent system as that employed for the osmylation.
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2O (3:1), which was the same solvent system as that employed for the osmylation.
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-
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21
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34548602171
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Conformer 17 was suggested to be the energetically most stable by Molecular mechanics calculations (MMFF, Macro Model 8.5).
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Conformer 17 was suggested to be the energetically most stable by Molecular mechanics calculations (MMFF, Macro Model 8.5).
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-
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24
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33845373603
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Prepared by Takai-Utimoto olefination of (E)-4-(Fmoc)amino-but-2- enal; see the Supporting Information and also K. Takai, K. Nitta, K. Utimoto, J. Am. Chem. Soc. 1986, 108, 7408-7410.
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Prepared by Takai-Utimoto olefination of (E)-4-(Fmoc)amino-but-2- enal; see the Supporting Information and also K. Takai, K. Nitta, K. Utimoto, J. Am. Chem. Soc. 1986, 108, 7408-7410.
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-
-
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26
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34548618902
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WO 2003006422
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Y. Watanabe, WO 2003006422.
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-
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Watanabe, Y.1
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29
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-
34548641322
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Prepared by a modified Kende procedure, where the method for the preparation of (Z)-2-methyl-5-(trimethylsilyl)pent-2-en-4-ynal, required for the key aldol reaction, was highly improved; see the Supporting Information.
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Prepared by a modified Kende procedure, where the method for the preparation of (Z)-2-methyl-5-(trimethylsilyl)pent-2-en-4-ynal, required for the key aldol reaction, was highly improved; see the Supporting Information.
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