Synthetic approach toward complexity of sialic acid-containing glycans
The biological relevance of sialic acid-containing glycans (sialo-glycans) to various interactions at the cell surface has increased the demand for the supply of structurally defined sialo-glycans. Due to their unique structures, the stereoselective synthesis of glycosides of sialic acid is inherent...
Gespeichert in:
Veröffentlicht in: | Bioscience, Biotechnology, and Biochemistry Biotechnology, and Biochemistry, 2015-03, Vol.79 (3), p.343-346 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 346 |
---|---|
container_issue | 3 |
container_start_page | 343 |
container_title | Bioscience, Biotechnology, and Biochemistry |
container_volume | 79 |
creator | Ando, Hiromune |
description | The biological relevance of sialic acid-containing glycans (sialo-glycans) to various interactions at the cell surface has increased the demand for the supply of structurally defined sialo-glycans. Due to their unique structures, the stereoselective synthesis of glycosides of sialic acid is inherently difficult, which makes the synthetic approach to synthesize diverse and complex sialo-glycans far from successful. However, the gap between the chemical and natural synthesis of complex sialo-glycans is narrowing through the emergence of synthetic methods. This review highlights recent progress made in the synthesis of complex sialo-glycans via cutting-edge synthetic methods.
The development of versatile synthetic units of sialic acid allowed to synthesize highly complicated sialic acid-containing molecules. |
doi_str_mv | 10.1080/09168451.2014.990228 |
format | Article |
fullrecord | <record><control><sourceid>proquest_oup_p</sourceid><recordid>TN_cdi_proquest_miscellaneous_1661333407</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1080/09168451.2014.990228</oup_id><sourcerecordid>1661333407</sourcerecordid><originalsourceid>FETCH-LOGICAL-c515t-fc68456e868333061d6bfcefaa38b2eac06d38107a7eb6d1ff8da56da78b428b3</originalsourceid><addsrcrecordid>eNqNkMtKxDAUhoMoznh5A5Eu3XRMmjRNVyKDNxhwoa7DaS4aaZuadBj79rZUXYqrA4fv_8_hQ-iM4BXBAl_iknDBcrLKMGGrssRZJvbQklBWpLxkxT5aTkg6MQt0FOM7xuMiJ4dokeWs5DRjS3T7NLT9m-mdSqDrggf1lvR-B0EnyjddbT5dPyTeJtFBPUHK6VT5tgfXuvY1ea0HBW08QQcW6mhOv-cxerm9eV7fp5vHu4f19SZVOcn71KrpZW4EF5RSzInmlVXGAlBRZQYU5poKggsoTMU1sVZoyLmGQlQsExU9Rhdz7_jqx9bEXjYuKlPX0Bq_jZJwTsZmhosRZTOqgo8xGCu74BoIgyRYTgblj0E5GZSzwTF2_n1hWzVG_4Z-lI3A5Qz4bfffyqs54VrrQwM7H2otexhqH2yAVrko6Z8NXwwejd4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1661333407</pqid></control><display><type>article</type><title>Synthetic approach toward complexity of sialic acid-containing glycans</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>Freely Accessible Japanese Titles</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Ando, Hiromune</creator><creatorcontrib>Ando, Hiromune</creatorcontrib><description>The biological relevance of sialic acid-containing glycans (sialo-glycans) to various interactions at the cell surface has increased the demand for the supply of structurally defined sialo-glycans. Due to their unique structures, the stereoselective synthesis of glycosides of sialic acid is inherently difficult, which makes the synthetic approach to synthesize diverse and complex sialo-glycans far from successful. However, the gap between the chemical and natural synthesis of complex sialo-glycans is narrowing through the emergence of synthetic methods. This review highlights recent progress made in the synthesis of complex sialo-glycans via cutting-edge synthetic methods.
The development of versatile synthetic units of sialic acid allowed to synthesize highly complicated sialic acid-containing molecules.</description><identifier>ISSN: 0916-8451</identifier><identifier>EISSN: 1347-6947</identifier><identifier>DOI: 10.1080/09168451.2014.990228</identifier><identifier>PMID: 25496324</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Chemistry Techniques, Synthetic - methods ; glycan ; Glycosylation ; Hydroxides - chemistry ; N-Acetylneuraminic Acid ; organic synthesis ; Polysaccharides - chemical synthesis ; Polysaccharides - chemistry ; sialic acid</subject><ispartof>Bioscience, Biotechnology, and Biochemistry, 2015-03, Vol.79 (3), p.343-346</ispartof><rights>2014 Japan Society for Bioscience, Biotechnology, and Agrochemistry 2014</rights><rights>2015 Japan Society for Bioscience, Biotechnology, and Agrochemistry 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-fc68456e868333061d6bfcefaa38b2eac06d38107a7eb6d1ff8da56da78b428b3</citedby><cites>FETCH-LOGICAL-c515t-fc68456e868333061d6bfcefaa38b2eac06d38107a7eb6d1ff8da56da78b428b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>313,314,776,780,788,27899,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25496324$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ando, Hiromune</creatorcontrib><title>Synthetic approach toward complexity of sialic acid-containing glycans</title><title>Bioscience, Biotechnology, and Biochemistry</title><addtitle>Biosci Biotechnol Biochem</addtitle><description>The biological relevance of sialic acid-containing glycans (sialo-glycans) to various interactions at the cell surface has increased the demand for the supply of structurally defined sialo-glycans. Due to their unique structures, the stereoselective synthesis of glycosides of sialic acid is inherently difficult, which makes the synthetic approach to synthesize diverse and complex sialo-glycans far from successful. However, the gap between the chemical and natural synthesis of complex sialo-glycans is narrowing through the emergence of synthetic methods. This review highlights recent progress made in the synthesis of complex sialo-glycans via cutting-edge synthetic methods.
The development of versatile synthetic units of sialic acid allowed to synthesize highly complicated sialic acid-containing molecules.</description><subject>Chemistry Techniques, Synthetic - methods</subject><subject>glycan</subject><subject>Glycosylation</subject><subject>Hydroxides - chemistry</subject><subject>N-Acetylneuraminic Acid</subject><subject>organic synthesis</subject><subject>Polysaccharides - chemical synthesis</subject><subject>Polysaccharides - chemistry</subject><subject>sialic acid</subject><issn>0916-8451</issn><issn>1347-6947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtKxDAUhoMoznh5A5Eu3XRMmjRNVyKDNxhwoa7DaS4aaZuadBj79rZUXYqrA4fv_8_hQ-iM4BXBAl_iknDBcrLKMGGrssRZJvbQklBWpLxkxT5aTkg6MQt0FOM7xuMiJ4dokeWs5DRjS3T7NLT9m-mdSqDrggf1lvR-B0EnyjddbT5dPyTeJtFBPUHK6VT5tgfXuvY1ea0HBW08QQcW6mhOv-cxerm9eV7fp5vHu4f19SZVOcn71KrpZW4EF5RSzInmlVXGAlBRZQYU5poKggsoTMU1sVZoyLmGQlQsExU9Rhdz7_jqx9bEXjYuKlPX0Bq_jZJwTsZmhosRZTOqgo8xGCu74BoIgyRYTgblj0E5GZSzwTF2_n1hWzVG_4Z-lI3A5Qz4bfffyqs54VrrQwM7H2otexhqH2yAVrko6Z8NXwwejd4</recordid><startdate>20150304</startdate><enddate>20150304</enddate><creator>Ando, Hiromune</creator><general>Taylor & Francis</general><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150304</creationdate><title>Synthetic approach toward complexity of sialic acid-containing glycans</title><author>Ando, Hiromune</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-fc68456e868333061d6bfcefaa38b2eac06d38107a7eb6d1ff8da56da78b428b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Chemistry Techniques, Synthetic - methods</topic><topic>glycan</topic><topic>Glycosylation</topic><topic>Hydroxides - chemistry</topic><topic>N-Acetylneuraminic Acid</topic><topic>organic synthesis</topic><topic>Polysaccharides - chemical synthesis</topic><topic>Polysaccharides - chemistry</topic><topic>sialic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ando, Hiromune</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioscience, Biotechnology, and Biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ando, Hiromune</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthetic approach toward complexity of sialic acid-containing glycans</atitle><jtitle>Bioscience, Biotechnology, and Biochemistry</jtitle><addtitle>Biosci Biotechnol Biochem</addtitle><date>2015-03-04</date><risdate>2015</risdate><volume>79</volume><issue>3</issue><spage>343</spage><epage>346</epage><pages>343-346</pages><issn>0916-8451</issn><eissn>1347-6947</eissn><abstract>The biological relevance of sialic acid-containing glycans (sialo-glycans) to various interactions at the cell surface has increased the demand for the supply of structurally defined sialo-glycans. Due to their unique structures, the stereoselective synthesis of glycosides of sialic acid is inherently difficult, which makes the synthetic approach to synthesize diverse and complex sialo-glycans far from successful. However, the gap between the chemical and natural synthesis of complex sialo-glycans is narrowing through the emergence of synthetic methods. This review highlights recent progress made in the synthesis of complex sialo-glycans via cutting-edge synthetic methods.
The development of versatile synthetic units of sialic acid allowed to synthesize highly complicated sialic acid-containing molecules.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>25496324</pmid><doi>10.1080/09168451.2014.990228</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0916-8451 |
ispartof | Bioscience, Biotechnology, and Biochemistry, 2015-03, Vol.79 (3), p.343-346 |
issn | 0916-8451 1347-6947 |
language | eng |
recordid | cdi_proquest_miscellaneous_1661333407 |
source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Freely Accessible Japanese Titles; EZB-FREE-00999 freely available EZB journals |
subjects | Chemistry Techniques, Synthetic - methods glycan Glycosylation Hydroxides - chemistry N-Acetylneuraminic Acid organic synthesis Polysaccharides - chemical synthesis Polysaccharides - chemistry sialic acid |
title | Synthetic approach toward complexity of sialic acid-containing glycans |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T18%3A25%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_oup_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthetic%20approach%20toward%20complexity%20of%20sialic%20acid-containing%20glycans&rft.jtitle=Bioscience,%20Biotechnology,%20and%20Biochemistry&rft.au=Ando,%20Hiromune&rft.date=2015-03-04&rft.volume=79&rft.issue=3&rft.spage=343&rft.epage=346&rft.pages=343-346&rft.issn=0916-8451&rft.eissn=1347-6947&rft_id=info:doi/10.1080/09168451.2014.990228&rft_dat=%3Cproquest_oup_p%3E1661333407%3C/proquest_oup_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1661333407&rft_id=info:pmid/25496324&rft_oup_id=10.1080/09168451.2014.990228&rfr_iscdi=true |