Source:http://linkedlifedata.com/resource/pubmed/id/21347475
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
13
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pubmed:dateCreated |
2011-3-16
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pubmed:abstractText |
A new strategy was developed for the direct conversion of furfural to 1,5-pentanediol by the hydrogenolysis of the furan ring under mild conditions based on Pt/Co(2)AlO(4) catalyst. This is the first report of the direct catalytic conversion of furfural to 1,5-pentanediol with high yield.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1,5-pentanediol,
http://linkedlifedata.com/resource/pubmed/chemical/Furaldehyde,
http://linkedlifedata.com/resource/pubmed/chemical/Furans,
http://linkedlifedata.com/resource/pubmed/chemical/Glycols,
http://linkedlifedata.com/resource/pubmed/chemical/Platinum,
http://linkedlifedata.com/resource/pubmed/chemical/furan
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1364-548X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
7
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pubmed:volume |
47
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3924-6
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pubmed:meshHeading | |
pubmed:year |
2011
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pubmed:articleTitle |
Direct catalytic conversion of furfural to 1,5-pentanediol by hydrogenolysis of the furan ring under mild conditions over Pt/Co2AlO4 catalyst.
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pubmed:affiliation |
Lab for Advanced Materials, Research Institute of Industrial Catalysis, East China University of Science and Technology, Shanghai 200237, P. R. China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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