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Sn-Beta catalysed conversion of hemicellulosic sugars

Holm, Martin S., Pagán-Torres, Yomaira J., Saravanamurugan, Shunmugavel, Riisager, Anders, Dumesic, James A., Taarning, Esben·2012·Green Chemistry

Abstract

Conversions of various pentoses and hexoses into methyl lactate has been demonstrated for the Sn-Beta catalyst. It is found that pentoses are converted to methyl lactate in slightly lower yields (∼40%) than what is obtained for hexoses (∼50%), but higher yields of glycolaldehyde dimethyl acetal are observed for the pentoses. This finding is in accordance to a reaction pathway that involves the retro aldol condensation of the sugars to form a triose and glycolaldehyde for the pentoses, and two trioses for hexoses. When reacting glycolaldehyde (formally a C2-sugar) in the presence of Sn-Beta, aldol condensation occurs, leading to the formation of methyl lactate, methyl vinylglycolate and methyl 2-hydroxy-4-methoxybutanoate. In contrast, when converting the sugars in water at low temperatures (100 °C), Sn-Beta catalyses the isomerisation of sugars (ketose–aldose epimers), rather than the formation of lactates.

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Metadata

Authors
Holm, M. S., Pagán-Torres, Y. J., Saravanamurugan, S., Riisager, A., Dumesic, J. A., & Taarning, E.
Venue
Green Chemistry
Published
2012
Volume
14
Issue
3
Pages
702
ISSN
  • 1463-9262 (ISSN-L)
  • 1463-9270
OpenAlex
W2148006161
Cited by
233
References
1
FWCI
11.68
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Sn-Beta catalysed conversion of hemicellulosic sugars. https://app.cochat.ai/papers/10.1039/c2gc16202d
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Holm, M. S., Pagán-Torres, Y. J., Saravanamurugan, S., Riisager, A., Dumesic, J. A., & Taarning, E. (2012). Sn-Beta catalysed conversion of hemicellulosic sugars. Green Chemistry. https://doi.org/10.1039/c2gc16202d

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