Phosha-Meerwein Reaction of Diazo Esters
Diazo esters (la,b) react with trialkyl phosphates (2a-c) in the presence of BF 3 .OEt 2 to give the corresponding phosphates (3a-e) in 42-58 % yields. The competed intra/intermolecular protonation in the reaction of la with dimethyl hydrogen phosphite leads to phosphonate. 4,and phosphite 5.
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Veröffentlicht in: | Phosphorus, sulfur, and silicon and the related elements sulfur, and silicon and the related elements, 1996-04, Vol.111 (1-4), p.155-155 |
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container_issue | 1-4 |
container_start_page | 155 |
container_title | Phosphorus, sulfur, and silicon and the related elements |
container_volume | 111 |
creator | Popov, Konstantin A. Polozov, Alexander M. |
description | Diazo esters (la,b) react with trialkyl phosphates (2a-c) in the presence of BF
3
.OEt
2
to give the corresponding phosphates (3a-e) in 42-58 % yields. The competed intra/intermolecular protonation in the reaction of la with dimethyl hydrogen phosphite leads to phosphonate. 4,and phosphite 5. |
doi_str_mv | 10.1080/10426509608054784 |
format | Article |
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3
.OEt
2
to give the corresponding phosphates (3a-e) in 42-58 % yields. The competed intra/intermolecular protonation in the reaction of la with dimethyl hydrogen phosphite leads to phosphonate. 4,and phosphite 5.</description><identifier>ISSN: 1042-6507</identifier><identifier>EISSN: 1563-5325</identifier><identifier>DOI: 10.1080/10426509608054784</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><subject>Diazo ester ; dimethyl hydrogen phosphite ; Lewis acid catalysis ; Phoshate ; zwitterionic phosphonium intermediate</subject><ispartof>Phosphorus, sulfur, and silicon and the related elements, 1996-04, Vol.111 (1-4), p.155-155</ispartof><rights>Copyright Taylor & Francis Group, LLC 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/10426509608054784$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/10426509608054784$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,59647,60436</link.rule.ids></links><search><creatorcontrib>Popov, Konstantin A.</creatorcontrib><creatorcontrib>Polozov, Alexander M.</creatorcontrib><title>Phosha-Meerwein Reaction of Diazo Esters</title><title>Phosphorus, sulfur, and silicon and the related elements</title><description>Diazo esters (la,b) react with trialkyl phosphates (2a-c) in the presence of BF
3
.OEt
2
to give the corresponding phosphates (3a-e) in 42-58 % yields. The competed intra/intermolecular protonation in the reaction of la with dimethyl hydrogen phosphite leads to phosphonate. 4,and phosphite 5.</description><subject>Diazo ester</subject><subject>dimethyl hydrogen phosphite</subject><subject>Lewis acid catalysis</subject><subject>Phoshate</subject><subject>zwitterionic phosphonium intermediate</subject><issn>1042-6507</issn><issn>1563-5325</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNp1j8tKA0EQRRtRMEY_wN0s3bRWv6fBjcT4gIii7pt-kpHJtHQPhPj1jsSduKoq7j0FB6FzApcEWrgiwKkUoOV0CK5afoBmREiGBaPicNqnHE8FdYxOav0AAE0ZzNDFyzrXtcVPMZZt7IbmNVo_dnlocmpuO_uVm2UdY6mn6CjZvsaz3zlHb3fL98UDXj3fPy5uVthrwbFy4LSjOpCgCLcgrAMFykVNg5IyUC1aIiCI1gUImnhJfOIksES9ZZzNEdl_9SXXWmIyn6Xb2LIzBMyPqPkjOjHXe6YbUi4bu82lD2a0uz6XVOzgu2rY__g3Ds5WvQ</recordid><startdate>19960401</startdate><enddate>19960401</enddate><creator>Popov, Konstantin A.</creator><creator>Polozov, Alexander M.</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19960401</creationdate><title>Phosha-Meerwein Reaction of Diazo Esters</title><author>Popov, Konstantin A. ; Polozov, Alexander M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c954-7b0b9b29d1d714a05ab0707be92d766d2958150d58bd0d91c61cf41d3f2ca343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Diazo ester</topic><topic>dimethyl hydrogen phosphite</topic><topic>Lewis acid catalysis</topic><topic>Phoshate</topic><topic>zwitterionic phosphonium intermediate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Popov, Konstantin A.</creatorcontrib><creatorcontrib>Polozov, Alexander M.</creatorcontrib><collection>CrossRef</collection><jtitle>Phosphorus, sulfur, and silicon and the related elements</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Popov, Konstantin A.</au><au>Polozov, Alexander M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phosha-Meerwein Reaction of Diazo Esters</atitle><jtitle>Phosphorus, sulfur, and silicon and the related elements</jtitle><date>1996-04-01</date><risdate>1996</risdate><volume>111</volume><issue>1-4</issue><spage>155</spage><epage>155</epage><pages>155-155</pages><issn>1042-6507</issn><eissn>1563-5325</eissn><abstract>Diazo esters (la,b) react with trialkyl phosphates (2a-c) in the presence of BF
3
.OEt
2
to give the corresponding phosphates (3a-e) in 42-58 % yields. The competed intra/intermolecular protonation in the reaction of la with dimethyl hydrogen phosphite leads to phosphonate. 4,and phosphite 5.</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/10426509608054784</doi><tpages>1</tpages></addata></record> |
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identifier | ISSN: 1042-6507 |
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issn | 1042-6507 1563-5325 |
language | eng |
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source | Taylor & Francis:Master (3349 titles) |
subjects | Diazo ester dimethyl hydrogen phosphite Lewis acid catalysis Phoshate zwitterionic phosphonium intermediate |
title | Phosha-Meerwein Reaction of Diazo Esters |
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