Ethers and Their Oligomeric Derivatives Obtained from 2,4,6,8-Tetra(hydroxymethyl)glycoluril
In this work, a series of 2,4,6,8-tetra(alkoxymethyl)glycoluril esters and their derivatives was synthesized for the first time, starting from 2,4,6,8-tetra(hydroxymethyl)glycoluril, the properties and spectral data of the synthesized compounds were described. Individual oligomers, derivatives of 2,...
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Veröffentlicht in: | Russian journal of general chemistry 2023-12, Vol.93 (Suppl 2), p.S456-S462 |
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container_issue | Suppl 2 |
container_start_page | S456 |
container_title | Russian journal of general chemistry |
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creator | Panshina, S. Yu Ponomarenko, О. V. Bakibaev, A. A. Malkov, V. S. Zhortarova, A. A. |
description | In this work, a series of 2,4,6,8-tetra(alkoxymethyl)glycoluril esters and their derivatives was synthesized for the first time, starting from 2,4,6,8-tetra(hydroxymethyl)glycoluril, the properties and spectral data of the synthesized compounds were described. Individual oligomers, derivatives of 2,4,6,8-tetra(methoxymethyl)glycoluril, were isolated and identified, their structures were described using HPLC analysis and IR and NMR spectroscopy. A similar possibility for the dimerization/oligomerization reactions of 2,4,6,8-tetra(ethoxymethyl)-, 2,4,6,8-tetra(isopropoxymethyl)-, and 2,4,6,8-tetra(butoxymethyl) derivatives of glycoluril with the release of macrocomponents was shown. |
doi_str_mv | 10.1134/S1070363223150069 |
format | Article |
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Yu ; Ponomarenko, О. V. ; Bakibaev, A. A. ; Malkov, V. S. ; Zhortarova, A. A.</creator><creatorcontrib>Panshina, S. Yu ; Ponomarenko, О. V. ; Bakibaev, A. A. ; Malkov, V. S. ; Zhortarova, A. A.</creatorcontrib><description>In this work, a series of 2,4,6,8-tetra(alkoxymethyl)glycoluril esters and their derivatives was synthesized for the first time, starting from 2,4,6,8-tetra(hydroxymethyl)glycoluril, the properties and spectral data of the synthesized compounds were described. Individual oligomers, derivatives of 2,4,6,8-tetra(methoxymethyl)glycoluril, were isolated and identified, their structures were described using HPLC analysis and IR and NMR spectroscopy. A similar possibility for the dimerization/oligomerization reactions of 2,4,6,8-tetra(ethoxymethyl)-, 2,4,6,8-tetra(isopropoxymethyl)-, and 2,4,6,8-tetra(butoxymethyl) derivatives of glycoluril with the release of macrocomponents was shown.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363223150069</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Dimerization ; Esters ; Ethers ; Infrared spectroscopy ; NMR spectroscopy ; Oligomerization ; Synthesis</subject><ispartof>Russian journal of general chemistry, 2023-12, Vol.93 (Suppl 2), p.S456-S462</ispartof><rights>Pleiades Publishing, Ltd. 2023</rights><rights>Pleiades Publishing, Ltd. 2023.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c268t-3b7aa5547a256fa24cf5a6aab5e6e7501f34e4974c72794214ddf1c2fabf0b313</cites><orcidid>0000-0001-9307-2342 ; 0000-0002-3335-3166 ; 0000-0001-6824-2645</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070363223150069$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070363223150069$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,41493,42562,51324</link.rule.ids></links><search><creatorcontrib>Panshina, S. Yu</creatorcontrib><creatorcontrib>Ponomarenko, О. V.</creatorcontrib><creatorcontrib>Bakibaev, A. A.</creatorcontrib><creatorcontrib>Malkov, V. S.</creatorcontrib><creatorcontrib>Zhortarova, A. A.</creatorcontrib><title>Ethers and Their Oligomeric Derivatives Obtained from 2,4,6,8-Tetra(hydroxymethyl)glycoluril</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>In this work, a series of 2,4,6,8-tetra(alkoxymethyl)glycoluril esters and their derivatives was synthesized for the first time, starting from 2,4,6,8-tetra(hydroxymethyl)glycoluril, the properties and spectral data of the synthesized compounds were described. Individual oligomers, derivatives of 2,4,6,8-tetra(methoxymethyl)glycoluril, were isolated and identified, their structures were described using HPLC analysis and IR and NMR spectroscopy. A similar possibility for the dimerization/oligomerization reactions of 2,4,6,8-tetra(ethoxymethyl)-, 2,4,6,8-tetra(isopropoxymethyl)-, and 2,4,6,8-tetra(butoxymethyl) derivatives of glycoluril with the release of macrocomponents was shown.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Dimerization</subject><subject>Esters</subject><subject>Ethers</subject><subject>Infrared spectroscopy</subject><subject>NMR spectroscopy</subject><subject>Oligomerization</subject><subject>Synthesis</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLw0AUhQdRsFZ_gLuAG4VG584zWUpbH1DowroTwiSZaVLyqDPTYv69Uyq4EDf3XjjfORcOQteA7wEoe3gDLDEVlBAKHGORnqARCJzElHJ8Gu4gxwf9HF04t8EYAkRG6GPuK21dpLoyWlW6ttGyqdd9q21dRLMw98rXe-2iZe5V3ekyMrZvIzJhEzFJ4pX2Vt1WQ2n7r6HVvhqau3UzFH2zs3Vzic6Mapy--tlj9P40X01f4sXy-XX6uIgLIhIf01wqxTmTinBhFGGF4UoolXMttOQYDGWapZIVksiUEWBlaaAgRuUG5xToGN0cc7e2_9xp57NNv7NdeJmRFCiATIAECo5UYXvnrDbZ1tatskMGODuUmP0pMXjI0eMC2621_U3-3_QNIOVy3g</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Panshina, S. Yu</creator><creator>Ponomarenko, О. V.</creator><creator>Bakibaev, A. A.</creator><creator>Malkov, V. S.</creator><creator>Zhortarova, A. A.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-9307-2342</orcidid><orcidid>https://orcid.org/0000-0002-3335-3166</orcidid><orcidid>https://orcid.org/0000-0001-6824-2645</orcidid></search><sort><creationdate>20231201</creationdate><title>Ethers and Their Oligomeric Derivatives Obtained from 2,4,6,8-Tetra(hydroxymethyl)glycoluril</title><author>Panshina, S. Yu ; Ponomarenko, О. V. ; Bakibaev, A. A. ; Malkov, V. S. ; Zhortarova, A. 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A.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Panshina, S. Yu</au><au>Ponomarenko, О. V.</au><au>Bakibaev, A. A.</au><au>Malkov, V. S.</au><au>Zhortarova, A. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ethers and Their Oligomeric Derivatives Obtained from 2,4,6,8-Tetra(hydroxymethyl)glycoluril</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2023-12-01</date><risdate>2023</risdate><volume>93</volume><issue>Suppl 2</issue><spage>S456</spage><epage>S462</epage><pages>S456-S462</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>In this work, a series of 2,4,6,8-tetra(alkoxymethyl)glycoluril esters and their derivatives was synthesized for the first time, starting from 2,4,6,8-tetra(hydroxymethyl)glycoluril, the properties and spectral data of the synthesized compounds were described. Individual oligomers, derivatives of 2,4,6,8-tetra(methoxymethyl)glycoluril, were isolated and identified, their structures were described using HPLC analysis and IR and NMR spectroscopy. A similar possibility for the dimerization/oligomerization reactions of 2,4,6,8-tetra(ethoxymethyl)-, 2,4,6,8-tetra(isopropoxymethyl)-, and 2,4,6,8-tetra(butoxymethyl) derivatives of glycoluril with the release of macrocomponents was shown.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363223150069</doi><orcidid>https://orcid.org/0000-0001-9307-2342</orcidid><orcidid>https://orcid.org/0000-0002-3335-3166</orcidid><orcidid>https://orcid.org/0000-0001-6824-2645</orcidid></addata></record> |
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subjects | Chemistry Chemistry and Materials Science Chemistry/Food Science Dimerization Esters Ethers Infrared spectroscopy NMR spectroscopy Oligomerization Synthesis |
title | Ethers and Their Oligomeric Derivatives Obtained from 2,4,6,8-Tetra(hydroxymethyl)glycoluril |
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