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13
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0025136899
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(a) Barton, D. H. R.; Augy-Dorey, S.; Camara, J.; Dalko, P.; Delaumény, J. M.; Géro, S. D.; Quiclet-Sire, B.; Stütz, P. Tetrahedron 1990, 46, 215.
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Géro, S.D.6
Quiclet-Sire, B.7
Stütz, P.8
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15
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85031227458
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note
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For the convenience, the term "gluco-, galacto-and manno-hexenopyranoside" express 6-deoxyhex-5-enopyranosides having the same C-2 to 4 configurations as glucose, galactose and mannose respectively in this paper.
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16
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85031231147
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note
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The substrates were prepared by conventional methods from glucose, galactose and mannose. The synthetic scheme of gluco-hexenopyranosides (1 and 3) is shown below as a representative of their preparations. (equation presented)
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17
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85031230028
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note
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2, toluene.
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-
-
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18
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85031215317
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note
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(b) BzCl, pyridine.
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-
-
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19
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85031217122
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note
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AgF, pyridine.
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-
-
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20
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85031224581
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note
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tBuOK, DMSO.
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21
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0027109449
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Machado, A. S.; Dubreuil, D.; Cleophax J.; Gero, S. D.; Thomas N. F. Carbohydr. Res. 1992, 233, C5.
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Machado, A.S.1
Dubreuil, D.2
Cleophax, J.3
Gero, S.D.4
Thomas, N.F.5
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22
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37049099792
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Blattner, R.; Ferrier, R. J.; Haines, S. R. J. Chem. Soc., Perkin Trans. 1 1985, 2413.
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Blattner, R.1
Ferrier, R.J.2
Haines, S.R.3
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23
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85077841182
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The similar low stereoselectivity have been observed in the Hg(II) mediated Ferrier rearrangement of 3: Semeria, D.; Philippe, M.; Delaumeny, J.-M.; Sepulchre, A.-M.; Géro, S. D. Synthesis 1983, 710.
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Synthesis
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Semeria, D.1
Philippe, M.2
Delaumeny, J.-M.3
Sepulchre, A.-M.4
Géro, S.D.5
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24
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84986437005
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The program MacroModel V4.0 was employed for the calculations: (a) Mohamadi, F.; Richards, N. G. J.; Guida, W. C.; Liskamp, R.; Lipton, M.; Caufield, C.; Chang, G.; Hendricson, T.; Still, W. C. J. Comput. Chem. 1990, 11, 440.
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Mohamadi, F.1
Richards, N.G.J.2
Guida, W.C.3
Liskamp, R.4
Lipton, M.5
Caufield, C.6
Chang, G.7
Hendricson, T.8
Still, W.C.9
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25
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0043162336
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The Monte Carlo conformational search was initially used to find conformers suitable for cyclization: (b) Cheng, G.; Guida, W. C.; Still, W. C. J. Am. Chem. Soc. 1989, 111, 4379.
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Cheng, G.1
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Still, W.C.3
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