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Hydrosilylation conditions applied on alkenyl benzylated xyloses: Selective reduction and isomerization

Applied Organometallic Chemistry (2009) 23(4) 161-164
DOI: 10.1002/aoc.1487
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Abstract

In the presence of triethylsilane and different transition metal catalysts, the main reactive pathways observed from benzylated xyloses bearing an unsaturated tether were the reduction and the isomerization of the double bond without debenzylation of the sugar moiety. Copyright © 2009 John Wiley & Sons, Ltd.

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Hadad, C., Bouquillon, S., Harakat, D., & Muzart, J. (2009). Hydrosilylation conditions applied on alkenyl benzylated xyloses: Selective reduction and isomerization. Applied Organometallic Chemistry, 23(4), 161–164. https://doi.org/10.1002/aoc.1487

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