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The Formation of Inherently Chiral Calix[4]quinolines by Doebner-Miller Reaction of Aldehydes and Aminocalixarenes
The formation of inherently chiral calix[4]arenes by the intramolecular cyclization approach suffers from a limited number of suitable substrates for these reactions. Here, we report an easy way to prepare one class of such compounds: calixquinolines, which can be obtained by the reaction of aldehyd...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2022-12, Vol.27 (23), p.8545 |
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description | The formation of inherently chiral calix[4]arenes by the intramolecular cyclization approach suffers from a limited number of suitable substrates for these reactions. Here, we report an easy way to prepare one class of such compounds: calixquinolines, which can be obtained by the reaction of aldehydes with easily accessible aminocalix[4]arenes in acidic conditions (Doebner-Miller reaction). The synthetic procedure represents a very straightforward approach to the inherently chiral macrocyclic systems. The complexation studies revealed the ability of these compounds to complex quaternary ammonium salts with different stoichiometries depending on the guest molecules. At the same time, the ability of enantioselective complexation of chiral
-methylammonium salts was demonstrated. |
doi_str_mv | 10.3390/molecules27238545 |
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-methylammonium salts was demonstrated.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules27238545</identifier><identifier>PMID: 36500638</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Aldehydes ; Ammonium ; Ammonium compounds ; Ammonium paratungstate ; Ammonium salts ; Aromatic compounds ; calixarene ; Chromatography ; Complexation ; Cyclization ; Enantiomers ; inherent chirality ; mercuration ; meta-substitution ; Miller, Von ; Organic compounds ; Quaternary Ammonium Compounds - chemistry ; Quaternary ammonium salts ; quinoline formation ; Quinolines ; Stoichiometry</subject><ispartof>Molecules (Basel, Switzerland), 2022-12, Vol.27 (23), p.8545</ispartof><rights>COPYRIGHT 2022 MDPI AG</rights><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-d6ae1a76846cee91664cf312ea8622dbee08641829d0ce36b808a726a8ca61d63</citedby><cites>FETCH-LOGICAL-c560t-d6ae1a76846cee91664cf312ea8622dbee08641829d0ce36b808a726a8ca61d63</cites><orcidid>0000-0003-3080-5283</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2748559005/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2748559005?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36500638$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tlustý, Martin</creatorcontrib><creatorcontrib>Eigner, Václav</creatorcontrib><creatorcontrib>Dvořáková, Hana</creatorcontrib><creatorcontrib>Lhoták, Pavel</creatorcontrib><title>The Formation of Inherently Chiral Calix[4]quinolines by Doebner-Miller Reaction of Aldehydes and Aminocalixarenes</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>The formation of inherently chiral calix[4]arenes by the intramolecular cyclization approach suffers from a limited number of suitable substrates for these reactions. Here, we report an easy way to prepare one class of such compounds: calixquinolines, which can be obtained by the reaction of aldehydes with easily accessible aminocalix[4]arenes in acidic conditions (Doebner-Miller reaction). The synthetic procedure represents a very straightforward approach to the inherently chiral macrocyclic systems. The complexation studies revealed the ability of these compounds to complex quaternary ammonium salts with different stoichiometries depending on the guest molecules. At the same time, the ability of enantioselective complexation of chiral
-methylammonium salts was demonstrated.</description><subject>Aldehydes</subject><subject>Ammonium</subject><subject>Ammonium compounds</subject><subject>Ammonium paratungstate</subject><subject>Ammonium salts</subject><subject>Aromatic compounds</subject><subject>calixarene</subject><subject>Chromatography</subject><subject>Complexation</subject><subject>Cyclization</subject><subject>Enantiomers</subject><subject>inherent chirality</subject><subject>mercuration</subject><subject>meta-substitution</subject><subject>Miller, Von</subject><subject>Organic compounds</subject><subject>Quaternary Ammonium Compounds - chemistry</subject><subject>Quaternary ammonium salts</subject><subject>quinoline formation</subject><subject>Quinolines</subject><subject>Stoichiometry</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl9rFDEUxQdRbK1-AF9kwBdftub_JC_CsrW6UBGkPomETHJnNyWTtMmOuN_erNvWrkoeEm7O-V3u4TbNS4xOKVXo7ZgC2ClAIR2hkjP-qDnGjKAZRUw9fvA-ap6VcoUQwQzzp80RFRwhQeVxky_X0J6nPJqNT7FNQ7uMa8gQN2HbLtY-m9AuTPA_v7HvN5OPKfgIpe237VmCPkKeffIhQG6_gLF3iHlwsN66qjPRtfOx2uyOYSoXyvPmyWBCgRe390nz9fz95eLj7OLzh-VifjGzXKDNzAkD2HRCMmEBFBaC2YFiAkYKQlwPgKRgWBLlkAUqeomk6Ygw0hqBnaAnzXLPdclc6evsR5O3OhmvfxdSXmmTN94G0FYxgXAvB-UMI30vFUZO9EJ0HAaObGW927Oup34EZ2s-NZkD6OFP9Gu9Sj-06qgQilXAm1tATjcTlI0efbEQgomQpqJJxynFktOuSl__Jb1KU441qqpiknOFEP-jWpk6gI9Dqn3tDqrnHeNKYIxpVZ3-R1WPg9HbFGHwtX5gwHuDzamUDMP9jBjp3dLpf5auel49DOfecbdl9BfdytSy</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Tlustý, Martin</creator><creator>Eigner, Václav</creator><creator>Dvořáková, Hana</creator><creator>Lhoták, Pavel</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-3080-5283</orcidid></search><sort><creationdate>20221201</creationdate><title>The Formation of Inherently Chiral Calix[4]quinolines by Doebner-Miller Reaction of Aldehydes and Aminocalixarenes</title><author>Tlustý, Martin ; Eigner, Václav ; Dvořáková, Hana ; Lhoták, Pavel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-d6ae1a76846cee91664cf312ea8622dbee08641829d0ce36b808a726a8ca61d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Aldehydes</topic><topic>Ammonium</topic><topic>Ammonium compounds</topic><topic>Ammonium paratungstate</topic><topic>Ammonium salts</topic><topic>Aromatic compounds</topic><topic>calixarene</topic><topic>Chromatography</topic><topic>Complexation</topic><topic>Cyclization</topic><topic>Enantiomers</topic><topic>inherent chirality</topic><topic>mercuration</topic><topic>meta-substitution</topic><topic>Miller, Von</topic><topic>Organic compounds</topic><topic>Quaternary Ammonium Compounds - chemistry</topic><topic>Quaternary ammonium salts</topic><topic>quinoline formation</topic><topic>Quinolines</topic><topic>Stoichiometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tlustý, Martin</creatorcontrib><creatorcontrib>Eigner, Václav</creatorcontrib><creatorcontrib>Dvořáková, Hana</creatorcontrib><creatorcontrib>Lhoták, Pavel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tlustý, Martin</au><au>Eigner, Václav</au><au>Dvořáková, Hana</au><au>Lhoták, Pavel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Formation of Inherently Chiral Calix[4]quinolines by Doebner-Miller Reaction of Aldehydes and Aminocalixarenes</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2022-12-01</date><risdate>2022</risdate><volume>27</volume><issue>23</issue><spage>8545</spage><pages>8545-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>The formation of inherently chiral calix[4]arenes by the intramolecular cyclization approach suffers from a limited number of suitable substrates for these reactions. 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subjects | Aldehydes Ammonium Ammonium compounds Ammonium paratungstate Ammonium salts Aromatic compounds calixarene Chromatography Complexation Cyclization Enantiomers inherent chirality mercuration meta-substitution Miller, Von Organic compounds Quaternary Ammonium Compounds - chemistry Quaternary ammonium salts quinoline formation Quinolines Stoichiometry |
title | The Formation of Inherently Chiral Calix[4]quinolines by Doebner-Miller Reaction of Aldehydes and Aminocalixarenes |
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