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Direct Assembly of 2-Oxazolidinones by Chemical Fixation of Carbon Dioxide
The reaction of β‐ and γ‐haloamines with carbon dioxide to give pharmaceutically relevant 2‐oxazolidinones and 1,3‐dioxazin‐2‐ones, was found to proceed efficiently in the presence of a base and in the absence of catalyst. After optimization of reaction conditions, the system was successfully expand...
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Published in: | Chemistry : a European journal 2014-07, Vol.20 (29), p.8867-8871 |
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container_issue | 29 |
container_start_page | 8867 |
container_title | Chemistry : a European journal |
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creator | Niemi, Teemu Perea-Buceta, Jesus E. Fernández, Israel Alakurtti, Sami Rantala, Erika Repo, Timo |
description | The reaction of β‐ and γ‐haloamines with carbon dioxide to give pharmaceutically relevant 2‐oxazolidinones and 1,3‐dioxazin‐2‐ones, was found to proceed efficiently in the presence of a base and in the absence of catalyst. After optimization of reaction conditions, the system was successfully expanded to a variety of haloamines, even at multigram scale. The reaction was further studied in silico by DFT calculations.
The reaction of β‐ and γ‐haloamines with carbon dioxide to give pharmaceutically relevant cyclic urethanes was found to proceed efficiently in the presence of a base and in the absence of catalyst (see figure). After optimization of reaction conditions, the system was expanded to a variety of haloamines, even at a multigram scale. The reaction was further studied in silico by DFT calculations. |
doi_str_mv | 10.1002/chem.201402368 |
format | article |
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The reaction of β‐ and γ‐haloamines with carbon dioxide to give pharmaceutically relevant cyclic urethanes was found to proceed efficiently in the presence of a base and in the absence of catalyst (see figure). After optimization of reaction conditions, the system was expanded to a variety of haloamines, even at a multigram scale. The reaction was further studied in silico by DFT calculations.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.201402368</identifier><identifier>PMID: 24905029</identifier><identifier>CODEN: CEUJED</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>2-oxazolidones ; antibiotics ; Assembly ; Carbon dioxide ; carbon dioxide activation ; carbon dioxide fixation ; Catalysts ; Chemistry ; density functional calculations ; Fixation ; Mathematical analysis ; Optimization ; Urethanes</subject><ispartof>Chemistry : a European journal, 2014-07, Vol.20 (29), p.8867-8871</ispartof><rights>2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5148-cdc0bd08c2c9f1a666e645381ccaaa6a72fc0ce7c92ac78180b67bdc8da5ee6d3</citedby><cites>FETCH-LOGICAL-c5148-cdc0bd08c2c9f1a666e645381ccaaa6a72fc0ce7c92ac78180b67bdc8da5ee6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24905029$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Niemi, Teemu</creatorcontrib><creatorcontrib>Perea-Buceta, Jesus E.</creatorcontrib><creatorcontrib>Fernández, Israel</creatorcontrib><creatorcontrib>Alakurtti, Sami</creatorcontrib><creatorcontrib>Rantala, Erika</creatorcontrib><creatorcontrib>Repo, Timo</creatorcontrib><title>Direct Assembly of 2-Oxazolidinones by Chemical Fixation of Carbon Dioxide</title><title>Chemistry : a European journal</title><addtitle>Chem. Eur. J</addtitle><description>The reaction of β‐ and γ‐haloamines with carbon dioxide to give pharmaceutically relevant 2‐oxazolidinones and 1,3‐dioxazin‐2‐ones, was found to proceed efficiently in the presence of a base and in the absence of catalyst. After optimization of reaction conditions, the system was successfully expanded to a variety of haloamines, even at multigram scale. The reaction was further studied in silico by DFT calculations.
The reaction of β‐ and γ‐haloamines with carbon dioxide to give pharmaceutically relevant cyclic urethanes was found to proceed efficiently in the presence of a base and in the absence of catalyst (see figure). After optimization of reaction conditions, the system was expanded to a variety of haloamines, even at a multigram scale. The reaction was further studied in silico by DFT calculations.</description><subject>2-oxazolidones</subject><subject>antibiotics</subject><subject>Assembly</subject><subject>Carbon dioxide</subject><subject>carbon dioxide activation</subject><subject>carbon dioxide fixation</subject><subject>Catalysts</subject><subject>Chemistry</subject><subject>density functional calculations</subject><subject>Fixation</subject><subject>Mathematical analysis</subject><subject>Optimization</subject><subject>Urethanes</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqF0Utv1DAUBWALgejQsmWJIrHpJoPfjpclfQGFVipQdpZzcyNckrjYM2KGX9-MpowQm67sxXeOZR1CXjE6Z5Tyt_ADhzmnTFIudPWEzJjirBRGq6dkRq00pVbC7pEXOd9SSq0W4jnZ49JSRbmdkQ_HISEsiqOccWj6dRG7gpeXK_8n9qENYxwxF826qKd3Avi-OA0rvwhx3MDap2a6HYe4Ci0ekGed7zO-fDj3ydfTky_1eXlxefa-ProoQTFZldACbVpaAQfbMa-1Ri2VqBiA9157wzuggAYs92AqVtFGm6aFqvUKUbdinxxue-9S_LXEvHBDyIB970eMy-yYMcZaqZh9nCpplBSMyom--Y_exmUap49slOBGW84mNd8qSDHnhJ27S2Hwae0YdZtB3GYQtxtkCrx-qF02A7Y7_neBCdgt-B16XD9S5-rzk0__lpfbbMgLXO2yPv102gij3M3nM3f9_WP17d3NlZPiHm__pYI</recordid><startdate>20140714</startdate><enddate>20140714</enddate><creator>Niemi, Teemu</creator><creator>Perea-Buceta, Jesus E.</creator><creator>Fernández, Israel</creator><creator>Alakurtti, Sami</creator><creator>Rantala, Erika</creator><creator>Repo, Timo</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20140714</creationdate><title>Direct Assembly of 2-Oxazolidinones by Chemical Fixation of Carbon Dioxide</title><author>Niemi, Teemu ; Perea-Buceta, Jesus E. ; Fernández, Israel ; Alakurtti, Sami ; Rantala, Erika ; Repo, Timo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5148-cdc0bd08c2c9f1a666e645381ccaaa6a72fc0ce7c92ac78180b67bdc8da5ee6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>2-oxazolidones</topic><topic>antibiotics</topic><topic>Assembly</topic><topic>Carbon dioxide</topic><topic>carbon dioxide activation</topic><topic>carbon dioxide fixation</topic><topic>Catalysts</topic><topic>Chemistry</topic><topic>density functional calculations</topic><topic>Fixation</topic><topic>Mathematical analysis</topic><topic>Optimization</topic><topic>Urethanes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Niemi, Teemu</creatorcontrib><creatorcontrib>Perea-Buceta, Jesus E.</creatorcontrib><creatorcontrib>Fernández, Israel</creatorcontrib><creatorcontrib>Alakurtti, Sami</creatorcontrib><creatorcontrib>Rantala, Erika</creatorcontrib><creatorcontrib>Repo, Timo</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Niemi, Teemu</au><au>Perea-Buceta, Jesus E.</au><au>Fernández, Israel</au><au>Alakurtti, Sami</au><au>Rantala, Erika</au><au>Repo, Timo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct Assembly of 2-Oxazolidinones by Chemical Fixation of Carbon Dioxide</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chem. Eur. J</addtitle><date>2014-07-14</date><risdate>2014</risdate><volume>20</volume><issue>29</issue><spage>8867</spage><epage>8871</epage><pages>8867-8871</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><coden>CEUJED</coden><abstract>The reaction of β‐ and γ‐haloamines with carbon dioxide to give pharmaceutically relevant 2‐oxazolidinones and 1,3‐dioxazin‐2‐ones, was found to proceed efficiently in the presence of a base and in the absence of catalyst. After optimization of reaction conditions, the system was successfully expanded to a variety of haloamines, even at multigram scale. The reaction was further studied in silico by DFT calculations.
The reaction of β‐ and γ‐haloamines with carbon dioxide to give pharmaceutically relevant cyclic urethanes was found to proceed efficiently in the presence of a base and in the absence of catalyst (see figure). After optimization of reaction conditions, the system was expanded to a variety of haloamines, even at a multigram scale. The reaction was further studied in silico by DFT calculations.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>24905029</pmid><doi>10.1002/chem.201402368</doi><tpages>5</tpages></addata></record> |
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subjects | 2-oxazolidones antibiotics Assembly Carbon dioxide carbon dioxide activation carbon dioxide fixation Catalysts Chemistry density functional calculations Fixation Mathematical analysis Optimization Urethanes |
title | Direct Assembly of 2-Oxazolidinones by Chemical Fixation of Carbon Dioxide |
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