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4
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0001508720
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Nakahara.Y.; Ogawa, T. Tetrahedron Lett. 1987, 28, 2731-2734. For the use of a bromo galacturonic acid ester as donor see: Lönn, H.; Lönngren, J. Carbohydr. Res. 1984, 132, 39-44.
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0021485528
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Nakahara.Y.; Ogawa, T. Tetrahedron Lett. 1987, 28, 2731-2734. For the use of a bromo galacturonic acid ester as donor see: Lönn, H.; Lönngren, J. Carbohydr. Res. 1984, 132, 39-44.
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For recent reviews see: a) Schmidt, R. R. Pure Appl. Chem. 1989, 61, 1257-1270.
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0028957029
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(c)Garegg, P. J.; Olsoon, L.; Oscarson, S. J. Org. Chem. 1995, 60, 2200-2204 and references therein.
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17
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0027964634
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Though phenyl thioglycosides are known to be less reactive than their alkyl counterparts (see ref 9d) they are more readily prepared and give about the same α-stereoselectivity (see : Sun, L.; Li, P.; Zhao, K. Tetrahedron Lett. 1994, 35, 7147-7150).
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Sun, L.1
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18
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0343737945
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L'Isle sur la Sorgue, France, 20-24th May
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ees Méditerranéennes des Glucides" L'Isle sur la Sorgue, France, 20-24th May 1996.
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ees Méditerranéennes des Glucides
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0000774185
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22
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a) Konradsson, P.; Udodong, U.E.; Fraser-Reid, B. Tetrahedron Lett. 1990, 31, 4313-4316.
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Konradsson, P.1
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23
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0025125757
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b) Veeneman, G.H.; van Leeuwen, S.H.; van Boom, J.H. Tetrahedron Lett. 1990, 31, 1331-1334.
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Veeneman, G.H.1
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Van Boom, J.H.3
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24
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0342867359
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note
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1,2 = 7.6 Hz), 102.7 (C-l), 99.9, 99.3 (C-1', C-l″).
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-
-
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25
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0342867358
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note
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4). The solvent was evaporated in vacuo and the crude product purified by chromatography on silicagel (eluents: 11α,12α, pentane/diethylether, 1/1; 13α,14α, pentane/ethyl acetate, 3/1; 15α, pentane/dichloromethane/diethylether, 6/4/0.5; 16α, pentane/diethylether, 3/1; 17α, dichloromethane/diethylether, 40/1).
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