Iodine–sodium cyanoborohydride-mediated reductive ring opening of 4,6-O-benzylidene acetals of hexopyranosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference44 articles.
1. Iodine and its Interhalogen Compounds: Versatile Reagents in Carbohydrate Chemistry-XXIV. For Part-XXIII see: Kartha, K. P. R.; Homans, S. W.; Field, R. A. Trends Carbohydr. Res. 2010, 2, 14–19. This work was presented in part at the meeting, ‘Chemistry Biology Interface: Synergistic New Frontiers’, held at Dr. B. R. Ambedkar Center for Biomedical Research, University of Delhi, P23–28, November 21–26, 2004. While this manuscript was in the process of preparation the following article was published: Regioselective Reductive Ring Opening of Benzylidene Acetals Using Triethylsilane and Iodine, Panchadhayee, R.; Misra, A. K. Synlett 2010, Advanced online publication: doi:10.1055/s-0029-1219798; Art ID: D02210ST.
2. Iodine, a novel catalyst in carbohydrate reactions I. -isopropylidination of carbohydrates
3. A new, facile method for cleavage of acetals and dithioacetals in carbohydrate derivatives
4. Carbohydrates;Robertson,2003
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