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1
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0029739240
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For a review on the use of glycals in organic synthesis, see
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For a review on the use of glycals in organic synthesis, see: Danishefsky, S.J.; Bilodeau, M.T. Angew. Chem., Int. Ed. Engl. 1996, 35, 1380.
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Danishefsky, S.J.1
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37049069691
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Csuk, R.; Fürstner, A; Glänzer, B.I.; Weidmann, H. J. Chem. Soc., Chem. Commun. 1986, 1149.
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Csuk, R.1
Fürstner, A.2
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8
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de Pouilly, P.; Chénedé, A.; Mallet, J.-M.; Sinaÿ, P. Bull. Soc. Chim. Fr. 1993, 130, 256.
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De Pouilly, P.1
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Sinaÿ, P.4
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0000036502
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a) Sekutowski, D.; Jungst, R.; Stucky, G.D. Inorg. Chem. 1978, 17, 1848;
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Sekutowski, D.1
Jungst, R.2
Stucky, G.D.3
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18
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0009566880
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note
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2TiCl in solution (see ref. 9a and b).
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19
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0009594997
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note
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It is interesting to note that in the case of acetobromogalactose and acetobromofucose as substrates (Table 1, entries 3 and 4), approximately 10% of 1-deoxy-2,3,4,6-tetra-O-acetyl-D-galactopyranose and to 1- deoxy-2,3,4-tri-O-acetyl-L-fucopyranose, resp., were isolated as side-products.
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20
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0342506470
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a) Skrydstrup, T.; Mazéas, D.; Elmouchir, M.; Doisneau, G.; Beau, J.-M.; Chem. Eur. J. 1997, 8, 1342;
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Chem. Eur. J.
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Skrydstrup, T.1
Mazéas, D.2
Elmouchir, M.3
Doisneau, G.4
Beau, J.-M.5
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21
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0031861064
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b) Skrydstrup, T.; Jarreton, O.; Mazéas, D.; Urban, D.; Beau, J.-M.; Chem. Eur. J., 1998, 4, 655;
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Chem. Eur. J.
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Skrydstrup, T.1
Jarreton, O.2
Mazéas, D.3
Urban, D.4
Beau, J.-M.5
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22
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0001272931
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c) Urban, D.; Skrydstrup, T.; Beau, J.-M.; J. Org. Chem., 1998, 63, 2507;
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J. Org. Chem.
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Urban, D.1
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Beau, J.-M.3
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24
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26844580582
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e) Andersen, L.; Mikkelsen, L.M.; Beau, J.- M.; Skrydstrup, T. Synlett 1998, 1393;
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Synlett
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Andersen, L.1
Mikkelsen, L.M.2
Beau, J.-M.3
Skrydstrup, T.4
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25
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0033041736
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f) Jarreton, O.; Skrydstrup, T.; Espinosa, J.-F.; Jiménez- Barbero, J.; Beau, J.-M. Chem. Eur. J., 1999, 5, 430.
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Jarreton, O.1
Skrydstrup, T.2
Espinosa, J.-F.3
Jiménez-Barbero, J.4
Beau, J.-M.5
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26
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0027094158
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For examples of the reductive samariation of glycosyl phenylsulfones for the preparation of glycals, see
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For examples of the reductive samariation of glycosyl phenylsulfones for the preparation of glycals, see, de Pouilly, P.; Chénedé, A.; Mallet, J.-M.; Sinaÿ, P. Tetrahedron Lett. 1992, 33, 8065.
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Tetrahedron Lett.
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Chénedé, A.2
Mallet, J.-M.3
Sinaÿ, P.4
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27
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0038527608
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2 as the catalyst and manganese as the stoichiometric reductant. a
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2 as the catalyst and manganese as the stoichiometric reductant. a) Gansäuer, A.; Moschioni, M.; Bauer, D. Eur. J. Org. Chem. 1998, 1923;
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Eur. J. Org. Chem.
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Gansäuer, A.1
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c) Gansäuer, A.; Bluhm, H.; Pierobon, M.; J. Am. Chem. Soc. 1998, 120, 12849.
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Gansäuer, A.1
Bluhm, H.2
Pierobon, M.3
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