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4
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0035416117
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For recent reviews, see: (a) Altmann, K. H. Curr. Opin. Chem. Biol. 2001, 5, 424. (b) He, L. F.; Orr, G. A.; Horwitz, S. B. Drug Discovery Today 2001, 6, 1153. (c) Stachel, S. J.; Biswas, K.; Danishefsky, S. J. Curr. Pharm. Des. 2001, 7, 1277.
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Altmann, K.H.1
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5
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For recent reviews, see: (a) Altmann, K. H. Curr. Opin. Chem. Biol. 2001, 5, 424. (b) He, L. F.; Orr, G. A.; Horwitz, S. B. Drug Discovery Today 2001, 6, 1153. (c) Stachel, S. J.; Biswas, K.; Danishefsky, S. J. Curr. Pharm. Des. 2001, 7, 1277.
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He, L.F.1
Orr, G.A.2
Horwitz, S.B.3
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6
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0034857182
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For recent reviews, see: (a) Altmann, K. H. Curr. Opin. Chem. Biol. 2001, 5, 424. (b) He, L. F.; Orr, G. A.; Horwitz, S. B. Drug Discovery Today 2001, 6, 1153. (c) Stachel, S. J.; Biswas, K.; Danishefsky, S. J. Curr. Pharm. Des. 2001, 7, 1277.
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Stachel, S.J.1
Biswas, K.2
Danishefsky, S.J.3
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7
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0029049468
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Bollag, D. M.; McQueney, P. A.; Zhu, J.; Hensens, O.; Koupal, L.; Liesch, J.; Goetz, M.; Lazarides, E.; Woods, C. M. Cancer Res. 1995, 55, 2325.
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Liesch, J.6
Goetz, M.7
Lazarides, E.8
Woods, C.M.9
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8
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0141602027
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note
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The absolute configuration of peloruside A has not yet been determined.
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9
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0041790924
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(a) Paterson, I.; Gibson, K. R.; Oballa, R. M. Tetrahedron Lett. 1996, 37, 8585.
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Paterson, I.1
Gibson, K.R.2
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11
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0000271703
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Evans, D.A.1
Coleman, P.J.2
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4444276636
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Kolb, H. C.; VanNieuwenhze, M. S.; Sharpless, K. B. Chem. Rev. 1994, 94, 2483.
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Kolb, H.C.1
VanNieuwenhze, M.S.2
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13
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0029147245
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For related studies on gem-dimethyl-containing substrates, see: Ohmori, K.; Nishiyama, S.; Yamamura, S. Tetrahedron Lett. 1995, 36, 6519.
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Ohmori, K.1
Nishiyama, S.2
Yamamura, S.3
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14
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0141825124
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note
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The enantiomeric purities of 9 and 14 were determined by chiral HPLC, using the racemic diol as the reference. The absolute configurations were determined by the advanced Mosher method (ref 18 and Supporting Information).
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-
-
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15
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0001015191
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Sharpless, K. B.; Amberg, W.; Beller, M.; Chen, H.; Hartung, J.; Kawanami, Y.; Lübben, D.; Manoury, E.; Ogino, Y.; Shibata, T.; Ukita, T. J. Org. Chem. 1991, 56, 4585.
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Sharpless, K.B.1
Amberg, W.2
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Chen, H.4
Hartung, J.5
Kawanami, Y.6
Lübben, D.7
Manoury, E.8
Ogino, Y.9
Shibata, T.10
Ukita, T.11
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16
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0000010197
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Oikawa, Y.; Yoshioka, T.; Yonemitsu, O. Tetrahedron Lett. 1982, 23, 889.
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Oikawa, Y.1
Yoshioka, T.2
Yonemitsu, O.3
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17
-
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0141713775
-
-
note
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This reaction was accompanied by the formation of the elimination product 2-(4-methoxybenzyloxymethyl)-5-methylfuran.
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19
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0028151214
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(b) Paterson, I.; Wallace, D. J.; Velázquez, S. M. Tetrahedron Lett. 1994, 35, 9083.
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Paterson, I.1
Wallace, D.J.2
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20
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0141490497
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note
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Ketone 17 was prepared from ethyl (S)-lactate in 62% yield by an identical 3-step sequence to that described in ref 13a for the enantiomeric series.
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-
-
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21
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0141490496
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note
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See the Supporting Information for a proof of stereochemistry of aldol adduct 18.
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23
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0000194961
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(a) Paterson, I.; Goodman, J. M.; Lister, M. A.; Schumann, R. C.; McClure, C. K.; Norcross, R. D. Tetrahedron 1990, 46, 4663.
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Paterson, I.1
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McClure, C.K.5
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25
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16144363676
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(c) Paterson, I.; Oballa, R. M.; Norcross, R. D. Tetrahedron Lett. 1996, 37, 8581.
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Paterson, I.1
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26
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0026525675
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1H NMR analysis of the corresponding (R)- and (S)-MTPA esters, using the advanced Mosher method, see: Kusumi, T.; Hamada, T.; Ishitsuka, M. O.; Ohtani, I.; Kakisawa, H. J. Org. Chem. 1992, 57, 1033.
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Kusumi, T.1
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Kakisawa, H.5
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27
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0035813890
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2 stereocenter. For a situation where more remote stereocenters win out over the 1,5-effect, see: Paterson, I.; Chen, D. Y.-K.; Coster, M. J.; Aceña, J. L.; Bach, J.; Gibson, K. R.; Keown, L. E.; Oballa, R. M.; Trieselmann, T.; Wallace, D. J.; Hodgson, A. P.; Norcross, R. D. Angew. Chem., Int. Ed. 2001, 40, 4055.
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Paterson, I.1
Chen, D.Y.-K.2
Coster, M.J.3
Aceña, J.L.4
Bach, J.5
Gibson, K.R.6
Keown, L.E.7
Oballa, R.M.8
Trieselmann, T.9
Wallace, D.J.10
Hodgson, A.P.11
Norcross, R.D.12
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