| Microwave-assisted Maillard reactions for the preparation of advanced glycation end products (AGEs). | |
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MedLine Citation:
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PMID: 20448908 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The application of microwaves as an efficient form of volumetric heating to promote organic reactions was recognized in the mid-1980 s. It has a much longer history in the food research and industry where microwave irradiation was studied in depth to optimize food browning and the development of desirable flavours from Maillard reactions. The microwave-promoted Maillard reaction is a challenging synthetic method to generate molecular diversity in a straightforward way. In this paper we present a new rapid and efficient one-pot procedure for the preparation of pentosidine and other AGEs under microwave irradiation. |
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Authors:
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Sonja Visentin; Claudio Medana; Alessandro Barge; Valeria Giancotti; Giancarlo Cravotto |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2010-03-25 |
Journal Detail:
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Title: Organic & biomolecular chemistry Volume: 8 ISSN: 1477-0539 ISO Abbreviation: Org. Biomol. Chem. Publication Date: 2010 May |
Date Detail:
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Created Date: 2010-05-07 Completed Date: 2010-08-12 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101154995 Medline TA: Org Biomol Chem Country: England |
Other Details:
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Languages: eng Pagination: 2473-7 Citation Subset: IM |
Affiliation:
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Dipartimento di Scienza e Tecnologia del Farmaco, Università di Torino, via P. Giuria 9, 10125 Torino, Italy. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Arginine
/
analogs & derivatives,
chemical synthesis,
chemistry Chromatography, High Pressure Liquid Chromatography, Liquid Glycosylation End Products, Advanced / chemical synthesis*, chemistry Gold Compounds / chemical synthesis, chemistry Imidazoles / chemical synthesis, chemistry Indicators and Reagents Kinetics Lysine / analogs & derivatives, chemical synthesis, chemistry Maillard Reaction / radiation effects* Mass Spectrometry Microwaves* |
| Chemical | |
Reg. No./Substance:
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0/1,3-bis(5-amino-5-carboxypentyl)-4-methyl-1H-imidazolium; 0/Glycosylation End Products, Advanced; 0/Gold Compounds; 0/Imidazoles; 0/Indicators and Reagents; 124505-87-9/pentosidine; 56-87-1/Lysine; 74-79-3/Arginine |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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