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and (c) McDonald, F. E.; Reddy, K. S.; Diaz, Y. Stereoselective Glycosylations ofa Family of 6-Deoxy-1,2-glycals Generated by Catalytic Alkynol Cyclo-Isomerization. J. Am. Chem. Soc. 2000, 122, 4304-4309.
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For other approaches to deoxysugars. see: A Rohr, J.; Wohlert, S. E.; Oelkers, C.; Kirschning, A.; Ries, M. Biosynthetic short activation of the 2,3,6-tndeoxy sugar L-rhodinose. Chem. Commun. 1997, 973-974.
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The attempts at the selective hydrolysis of digitoxin to form digoxose has been futile, only the monosaccharide digitoxose was isolated. Surprisingly, digoxose can be isolated from the dried twigs of Orthenthera viminea, seq: Tiwari, K. N.; Khare, N. K.; Khare, A.; Khare, M. P. Structure of digoxose. Carbohydr. Res. 1984, 129, 179-187.
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The attempts at the selective hydrolysis of digitoxin to form digoxose has been futile, only the monosaccharide digitoxose was isolated. Surprisingly, digoxose can be isolated from the dried twigs of Orthenthera viminea, seq: Tiwari, K. N.; Khare, N. K.; Khare, A.; Khare, M. P. Structure of digoxose. Carbohydr. Res. 1984, 129, 179-187.
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