Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids

Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids

Looking forward: As fossil fuels deplete, 5-hydroxymethylfurfural (HMF) will play an important role in securing future energy and chemical feedstock needs as it is obtainable from renewable resources such as glucose and cellulose. We report a group of nonmetal Lewis-acid arylboronic acids that catal...

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Main Authors: Lukamto, Daniel H., Wang, Peng, Loh, Teck-Peng
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2014
Subjects:
DRNTU::Science::Chemistry::Organic chemistry
Online Access:https://hdl.handle.net/10356/101885
http://hdl.handle.net/10220/19788
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1018852020-03-07T12:34:54Z Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids Lukamto, Daniel H. Wang, Peng Loh, Teck-Peng School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry Looking forward: As fossil fuels deplete, 5-hydroxymethylfurfural (HMF) will play an important role in securing future energy and chemical feedstock needs as it is obtainable from renewable resources such as glucose and cellulose. We report a group of nonmetal Lewis-acid arylboronic acids that catalyse the formation of HMF in 3-ethyl-1-methyl-3 H-imidazol-1-ium chloride ([EMIM]Cl) from glucose and cellulose. EWG=electron-withdrawing group. 2014-06-16T03:49:21Z 2019-12-06T20:46:18Z 2014-06-16T03:49:21Z 2019-12-06T20:46:18Z 2013 2013 Journal Article Lukamto, D. H., Wang, P., & Loh, T.-P. (2013). Catalytic Conversion of Inert Carbohydrates into Platform Chemical 5-Hydroxymethylfurfural Using Arylboronic Acids. Asian Journal of Organic Chemistry, 2(11), 947-951. 2193-5807 https://hdl.handle.net/10356/101885 http://hdl.handle.net/10220/19788 10.1002/ajoc.201300185 en Asian journal of organic chemistry © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science::Chemistry::Organic chemistry
spellingShingle DRNTU::Science::Chemistry::Organic chemistry
Lukamto, Daniel H.
Wang, Peng
Loh, Teck-Peng
Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids
description Looking forward: As fossil fuels deplete, 5-hydroxymethylfurfural (HMF) will play an important role in securing future energy and chemical feedstock needs as it is obtainable from renewable resources such as glucose and cellulose. We report a group of nonmetal Lewis-acid arylboronic acids that catalyse the formation of HMF in 3-ethyl-1-methyl-3 H-imidazol-1-ium chloride ([EMIM]Cl) from glucose and cellulose. EWG=electron-withdrawing group.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Lukamto, Daniel H.
Wang, Peng
Loh, Teck-Peng
format Article
author Lukamto, Daniel H.
Wang, Peng
Loh, Teck-Peng
author_sort Lukamto, Daniel H.
title Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids
title_short Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids
title_full Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids
title_fullStr Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids
title_full_unstemmed Catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids
title_sort catalytic conversion of inert carbohydrates into platform chemical 5-hydroxymethylfurfural using arylboronic acids
publishDate 2014
url https://hdl.handle.net/10356/101885
http://hdl.handle.net/10220/19788
_version_ 1681039234534735872

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