Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?
Changes in concentration (0.001–0.1 M) of an arabinofuranosyl donor (1) have been shown to modulate the temperature T at which activation of 1 occurs (from −23 °C to +7 °C), the reaction time (from 1.5 h to 3 days) and the yield of the disaccharide formed (from 14% to 82%). At concentrations exceedi...
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Veröffentlicht in: | Carbohydrate research 2017-01, Vol.437, p.28-35 |
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creator | Kononov, Leonid O. Fedina, Ksenia G. Orlova, Anna V. Kondakov, Nikolay N. Abronina, Polina I. Podvalnyy, Nikita M. Chizhov, Alexander O. |
description | Changes in concentration (0.001–0.1 M) of an arabinofuranosyl donor (1) have been shown to modulate the temperature T at which activation of 1 occurs (from −23 °C to +7 °C), the reaction time (from 1.5 h to 3 days) and the yield of the disaccharide formed (from 14% to 82%). At concentrations exceeding 0.01 M, these parameters, as well as the specific optical rotation of the solution of 1, virtually do not depend on concentration suggesting formation of reacting species (supramers) of glycosyl donor with similar structures, hence reactivities, but considerably different from those formed in more dilute solutions. The found critical concentration (0.01 M) separates two concentration ranges of reaction solutions corresponding to two types of solution structure that are featured by the presence of fundamentally different supramers of glycosyl donor, which have distinct chemical properties. These results allow a fresh look at the problems of reactivity of chemical compounds and selectivity of the reactions in which they participate.
[Display omitted]
•Influence of concentration on outcome of arabinofuranosylation was studied.•Two concentration ranges of solutions with different structures were revealed.•Bimodal reactivity pattern of glycosyl donor was discovered.•Bimodality was linked to the presence of two types of supramers of glycosyl donor. |
doi_str_mv | 10.1016/j.carres.2016.11.009 |
format | Article |
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[Display omitted]
•Influence of concentration on outcome of arabinofuranosylation was studied.•Two concentration ranges of solutions with different structures were revealed.•Bimodal reactivity pattern of glycosyl donor was discovered.•Bimodality was linked to the presence of two types of supramers of glycosyl donor.</description><identifier>ISSN: 0008-6215</identifier><identifier>EISSN: 1873-426X</identifier><identifier>DOI: 10.1016/j.carres.2016.11.009</identifier><identifier>PMID: 27883907</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Arabinofuranose ; Arabinose - analogs & derivatives ; Arabinose - chemistry ; Benzyl-free approach ; Carbohydrate Biochemistry - methods ; Carbohydrate Conformation ; Concentration ; Disaccharides - chemistry ; Glycosylation ; Reactivity ; Solutions ; Supramer ; Temperature</subject><ispartof>Carbohydrate research, 2017-01, Vol.437, p.28-35</ispartof><rights>2016 Elsevier Ltd</rights><rights>Copyright © 2016 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-1c2ce9e4cb11a7e527da1b11bd0b6eb954807deaa9a038f1e5bb2716260918b23</citedby><cites>FETCH-LOGICAL-c362t-1c2ce9e4cb11a7e527da1b11bd0b6eb954807deaa9a038f1e5bb2716260918b23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.carres.2016.11.009$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27883907$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kononov, Leonid O.</creatorcontrib><creatorcontrib>Fedina, Ksenia G.</creatorcontrib><creatorcontrib>Orlova, Anna V.</creatorcontrib><creatorcontrib>Kondakov, Nikolay N.</creatorcontrib><creatorcontrib>Abronina, Polina I.</creatorcontrib><creatorcontrib>Podvalnyy, Nikita M.</creatorcontrib><creatorcontrib>Chizhov, Alexander O.</creatorcontrib><title>Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?</title><title>Carbohydrate research</title><addtitle>Carbohydr Res</addtitle><description>Changes in concentration (0.001–0.1 M) of an arabinofuranosyl donor (1) have been shown to modulate the temperature T at which activation of 1 occurs (from −23 °C to +7 °C), the reaction time (from 1.5 h to 3 days) and the yield of the disaccharide formed (from 14% to 82%). At concentrations exceeding 0.01 M, these parameters, as well as the specific optical rotation of the solution of 1, virtually do not depend on concentration suggesting formation of reacting species (supramers) of glycosyl donor with similar structures, hence reactivities, but considerably different from those formed in more dilute solutions. The found critical concentration (0.01 M) separates two concentration ranges of reaction solutions corresponding to two types of solution structure that are featured by the presence of fundamentally different supramers of glycosyl donor, which have distinct chemical properties. These results allow a fresh look at the problems of reactivity of chemical compounds and selectivity of the reactions in which they participate.
[Display omitted]
•Influence of concentration on outcome of arabinofuranosylation was studied.•Two concentration ranges of solutions with different structures were revealed.•Bimodal reactivity pattern of glycosyl donor was discovered.•Bimodality was linked to the presence of two types of supramers of glycosyl donor.</description><subject>Arabinofuranose</subject><subject>Arabinose - analogs & derivatives</subject><subject>Arabinose - chemistry</subject><subject>Benzyl-free approach</subject><subject>Carbohydrate Biochemistry - methods</subject><subject>Carbohydrate Conformation</subject><subject>Concentration</subject><subject>Disaccharides - chemistry</subject><subject>Glycosylation</subject><subject>Reactivity</subject><subject>Solutions</subject><subject>Supramer</subject><subject>Temperature</subject><issn>0008-6215</issn><issn>1873-426X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1LxDAQxYMoun78ByI5emnNpG3aelBU_ALBi4K3kCazmrXbrEm6sP-9WVY9epp58N4b5kfIMbAcGIizWa6V9xhynlQOkDPWbpEJNHWRlVy8bZMJY6zJBIdqj-yHMEuSiVrskj1eN03RsnpCPq_t3BnVU-0GjUP0Klo3ZAYXOJikqUelo13auKILFSP6gbopVfS9X2kXVj01bnD-nD4GGj-QBteP6wYaoh91HD1SOyxdv0RzeUh2pqoPePQzD8jr3e3LzUP29Hz_eHP1lOlC8JiB5hpbLHUHoGqseG0UpL0zrBPYtVXZsNqgUq1iRTMFrLqO1yC4YC00HS8OyOmmd-Hd14ghyrkNGvteDejGIKEpS8ZFKapkLTdW7V0IHqdy4e1c-ZUEJteY5UxuMMs1ZgkgE-YUO_m5MHZzNH-hX67JcLExYPpzadHLoC0mwsZ61FEaZ_-_8A1dxZK1</recordid><startdate>20170102</startdate><enddate>20170102</enddate><creator>Kononov, Leonid O.</creator><creator>Fedina, Ksenia G.</creator><creator>Orlova, Anna V.</creator><creator>Kondakov, Nikolay N.</creator><creator>Abronina, Polina I.</creator><creator>Podvalnyy, Nikita M.</creator><creator>Chizhov, Alexander O.</creator><general>Elsevier Ltd</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>20170102</creationdate><title>Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?</title><author>Kononov, Leonid O. ; Fedina, Ksenia G. ; Orlova, Anna V. ; Kondakov, Nikolay N. ; Abronina, Polina I. ; Podvalnyy, Nikita M. ; Chizhov, Alexander O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-1c2ce9e4cb11a7e527da1b11bd0b6eb954807deaa9a038f1e5bb2716260918b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Arabinofuranose</topic><topic>Arabinose - analogs & derivatives</topic><topic>Arabinose - chemistry</topic><topic>Benzyl-free approach</topic><topic>Carbohydrate Biochemistry - methods</topic><topic>Carbohydrate Conformation</topic><topic>Concentration</topic><topic>Disaccharides - chemistry</topic><topic>Glycosylation</topic><topic>Reactivity</topic><topic>Solutions</topic><topic>Supramer</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kononov, Leonid O.</creatorcontrib><creatorcontrib>Fedina, Ksenia G.</creatorcontrib><creatorcontrib>Orlova, Anna V.</creatorcontrib><creatorcontrib>Kondakov, Nikolay N.</creatorcontrib><creatorcontrib>Abronina, Polina I.</creatorcontrib><creatorcontrib>Podvalnyy, Nikita M.</creatorcontrib><creatorcontrib>Chizhov, Alexander O.</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>Carbohydrate research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kononov, Leonid O.</au><au>Fedina, Ksenia G.</au><au>Orlova, Anna V.</au><au>Kondakov, Nikolay N.</au><au>Abronina, Polina I.</au><au>Podvalnyy, Nikita M.</au><au>Chizhov, Alexander O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?</atitle><jtitle>Carbohydrate research</jtitle><addtitle>Carbohydr Res</addtitle><date>2017-01-02</date><risdate>2017</risdate><volume>437</volume><spage>28</spage><epage>35</epage><pages>28-35</pages><issn>0008-6215</issn><eissn>1873-426X</eissn><abstract>Changes in concentration (0.001–0.1 M) of an arabinofuranosyl donor (1) have been shown to modulate the temperature T at which activation of 1 occurs (from −23 °C to +7 °C), the reaction time (from 1.5 h to 3 days) and the yield of the disaccharide formed (from 14% to 82%). At concentrations exceeding 0.01 M, these parameters, as well as the specific optical rotation of the solution of 1, virtually do not depend on concentration suggesting formation of reacting species (supramers) of glycosyl donor with similar structures, hence reactivities, but considerably different from those formed in more dilute solutions. The found critical concentration (0.01 M) separates two concentration ranges of reaction solutions corresponding to two types of solution structure that are featured by the presence of fundamentally different supramers of glycosyl donor, which have distinct chemical properties. These results allow a fresh look at the problems of reactivity of chemical compounds and selectivity of the reactions in which they participate.
[Display omitted]
•Influence of concentration on outcome of arabinofuranosylation was studied.•Two concentration ranges of solutions with different structures were revealed.•Bimodal reactivity pattern of glycosyl donor was discovered.•Bimodality was linked to the presence of two types of supramers of glycosyl donor.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>27883907</pmid><doi>10.1016/j.carres.2016.11.009</doi><tpages>8</tpages></addata></record> |
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subjects | Arabinofuranose Arabinose - analogs & derivatives Arabinose - chemistry Benzyl-free approach Carbohydrate Biochemistry - methods Carbohydrate Conformation Concentration Disaccharides - chemistry Glycosylation Reactivity Solutions Supramer Temperature |
title | Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved? |
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