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Studies on the regioselective reductive ringcleavage reactions of 3,5-O-arylidene-D-xylofuranosides

Synthetic Communications, ISSN: 0039-7911, Vol: 33, Issue: 13, Page: 2349-2363
2003
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Article Description

Reductive ring cleavage of 3,5-O-arylidene-D-xylofuranosides using LiAlH-AlCl and NaBHCN-BF proceeded regioselectively to provide secondary alcohol as the major product. The effect of the substitutents on the selectivity is examined.

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