Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids
Room-temperature imidazolium ionic liquids [Rmim][X] (X = Br, BF 4, NTf 2) as a reaction medium change the reaction course of phosphorus(III) acid esters with primary alkyl halides, aryl bromides, and propargyl bromide to afford hydrophosphoryl compounds, products of oxidation of the starting phosph...
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| Veröffentlicht in: | Mendeleev communications 2010-05, Vol.20 (3), p.145-147 |
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| container_title | Mendeleev communications |
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| creator | Matveeva, Ekaterina V. Kozlov, Vladimir A. Odinets, Irina L. |
| description | Room-temperature imidazolium ionic liquids [Rmim][X] (X
=
Br, BF
4, NTf
2) as a reaction medium change the reaction course of phosphorus(III) acid esters with primary alkyl halides, aryl bromides, and propargyl bromide to afford hydrophosphoryl compounds, products of oxidation of the starting phosphorus substrates, and 2,3-bis(phosphoryl)prop-1-enes, respectively. |
| doi_str_mv | 10.1016/j.mencom.2010.05.007 |
| format | Article |
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2) as a reaction medium change the reaction course of phosphorus(III) acid esters with primary alkyl halides, aryl bromides, and propargyl bromide to afford hydrophosphoryl compounds, products of oxidation of the starting phosphorus substrates, and 2,3-bis(phosphoryl)prop-1-enes, respectively.</description><identifier>ISSN: 0959-9436</identifier><identifier>DOI: 10.1016/j.mencom.2010.05.007</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Alterations ; Aromatic compounds ; Bromides ; Esters ; Halides ; Ionic liquids ; Oxidation ; Phosphorus</subject><ispartof>Mendeleev communications, 2010-05, Vol.20 (3), p.145-147</ispartof><rights>2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-582f11a7e645b0f05069b73fe1e2bb0ee81acb8d0121fdf757da76d52f803b1a3</citedby><cites>FETCH-LOGICAL-c339t-582f11a7e645b0f05069b73fe1e2bb0ee81acb8d0121fdf757da76d52f803b1a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0959943610000738$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Matveeva, Ekaterina V.</creatorcontrib><creatorcontrib>Kozlov, Vladimir A.</creatorcontrib><creatorcontrib>Odinets, Irina L.</creatorcontrib><title>Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids</title><title>Mendeleev communications</title><description>Room-temperature imidazolium ionic liquids [Rmim][X] (X
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2) as a reaction medium change the reaction course of phosphorus(III) acid esters with primary alkyl halides, aryl bromides, and propargyl bromide to afford hydrophosphoryl compounds, products of oxidation of the starting phosphorus substrates, and 2,3-bis(phosphoryl)prop-1-enes, respectively.</description><subject>Alterations</subject><subject>Aromatic compounds</subject><subject>Bromides</subject><subject>Esters</subject><subject>Halides</subject><subject>Ionic liquids</subject><subject>Oxidation</subject><subject>Phosphorus</subject><issn>0959-9436</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kE1OwzAQhb0AiVK4AYss2SSM4zhONkhVxZ9UxAYWrCzHGauukrq1k0p0xR24ISfBUNgijTSap_eeNB8hFxQyCrS8WmU9rrXrsxyiBDwDEEdkAjWv07pg5Qk5DWEFUeWMTsjrrBvQq8G6deJMMiwx0W70Af-uR6uXCjsbPt8_Zr4Z926XeFT6J2Hj9LZVe9fZsU-iZHXS2e1o23BGjo3qAp7_7il5ub15nt-ni6e7h_lskWrG6iHlVW4oVQLLgjdggENZN4IZpJg3DSBWVOmmaoHm1LRGcNEqUbY8NxWwhio2JZeH3o132xHDIHsbNHadWqMbg6SloIzmhYBoLQ5W7V0IHo3ceNsr_yYpyG96ciUP9OQ3PQlcRk4xdn2IYXxjZ9HLoG20YWs96kG2zv5f8AVLG36g</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>Matveeva, Ekaterina V.</creator><creator>Kozlov, Vladimir A.</creator><creator>Odinets, Irina L.</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20100501</creationdate><title>Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids</title><author>Matveeva, Ekaterina V. ; Kozlov, Vladimir A. ; Odinets, Irina L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-582f11a7e645b0f05069b73fe1e2bb0ee81acb8d0121fdf757da76d52f803b1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Alterations</topic><topic>Aromatic compounds</topic><topic>Bromides</topic><topic>Esters</topic><topic>Halides</topic><topic>Ionic liquids</topic><topic>Oxidation</topic><topic>Phosphorus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matveeva, Ekaterina V.</creatorcontrib><creatorcontrib>Kozlov, Vladimir A.</creatorcontrib><creatorcontrib>Odinets, Irina L.</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Mendeleev communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matveeva, Ekaterina V.</au><au>Kozlov, Vladimir A.</au><au>Odinets, Irina L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids</atitle><jtitle>Mendeleev communications</jtitle><date>2010-05-01</date><risdate>2010</risdate><volume>20</volume><issue>3</issue><spage>145</spage><epage>147</epage><pages>145-147</pages><issn>0959-9436</issn><abstract>Room-temperature imidazolium ionic liquids [Rmim][X] (X
=
Br, BF
4, NTf
2) as a reaction medium change the reaction course of phosphorus(III) acid esters with primary alkyl halides, aryl bromides, and propargyl bromide to afford hydrophosphoryl compounds, products of oxidation of the starting phosphorus substrates, and 2,3-bis(phosphoryl)prop-1-enes, respectively.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.mencom.2010.05.007</doi><tpages>3</tpages></addata></record> |
| fulltext | fulltext |
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| ispartof | Mendeleev communications, 2010-05, Vol.20 (3), p.145-147 |
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| source | Elsevier ScienceDirect Journals Complete |
| subjects | Alterations Aromatic compounds Bromides Esters Halides Ionic liquids Oxidation Phosphorus |
| title | Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids |
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