Synthesis of [1,2-14C]trichloroacetic acid
A growing interest in the phytotoxic effects of trichloroacetic acid (TCA) has led us to develop a small‐scale (70% yield and specific activity of 3.7 GBq/mmol. Copyright © 2001 John Wiley & Sons, Ltd.
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Veröffentlicht in: | Journal of labelled compounds & radiopharmaceuticals 2001-10, Vol.44 (11), p.811-814 |
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container_issue | 11 |
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container_title | Journal of labelled compounds & radiopharmaceuticals |
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creator | Bubner, M. Fuksová, K. Matucha, M. Heise, K. H. Bernhard, G. |
description | A growing interest in the phytotoxic effects of trichloroacetic acid (TCA) has led us to develop a small‐scale (70% yield and specific activity of 3.7 GBq/mmol. Copyright © 2001 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jlcr.505 |
format | Article |
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H. ; Bernhard, G.</creator><creatorcontrib>Bubner, M. ; Fuksová, K. ; Matucha, M. ; Heise, K. H. ; Bernhard, G.</creatorcontrib><description>A growing interest in the phytotoxic effects of trichloroacetic acid (TCA) has led us to develop a small‐scale (<1 mmol) one‐pot synthesis of [1,2‐14C]TCA with >70% yield and specific activity of 3.7 GBq/mmol. 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H.</creatorcontrib><creatorcontrib>Bernhard, G.</creatorcontrib><title>Synthesis of [1,2-14C]trichloroacetic acid</title><title>Journal of labelled compounds & radiopharmaceuticals</title><addtitle>J Label Compd Radiopharm</addtitle><description>A growing interest in the phytotoxic effects of trichloroacetic acid (TCA) has led us to develop a small‐scale (<1 mmol) one‐pot synthesis of [1,2‐14C]TCA with >70% yield and specific activity of 3.7 GBq/mmol. Copyright © 2001 John Wiley & Sons, Ltd.</description><subject>2-14C]trichloroacetic acid</subject><subject>[1,2‐14C]trichloroacetic acid</subject><subject>Aliphatic compounds</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>one-pot synthesis</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><issn>0362-4803</issn><issn>1099-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1z0tLAzEUBeAgCtYq-BO6EURMvXlOZ2mntlqKgg9ciIQ0D5o6dkoyoP33TpmiK1f3wP04cBA6JdAnAPRqWZrYFyD2UIdAnmPCON9HHWCSYj4AdoiOUloCND_OO-jiabOqFy6F1Kt8741cUkx48V7HYBZlFSttXB1MT5tgj9GB12VyJ7vbRS_jm-fiFs8eJnfF9QwbxojAzEsH0lPrqLESLHPamwyaYK2mhno9l8IxkVM3YJQTK6TQHnw2Fzwn1rMuOm97TaxSis6rdQyfOm4UAbXdqLYbVbOxoWctXetkdOmjXpmQ_jwHSSmQxuHWfYXSbf7tU9NZ8dj27nxItfv-9Tp-KJmxTKjX-4kaTofjEYyImrAfx2Rtug</recordid><startdate>20011015</startdate><enddate>20011015</enddate><creator>Bubner, M.</creator><creator>Fuksová, K.</creator><creator>Matucha, M.</creator><creator>Heise, K. 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H. ; Bernhard, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3315-3f6e06f2de2cd60d3eafc700d3dda2c2fab65e3592e83241d565af0f7b5491df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>2-14C]trichloroacetic acid</topic><topic>[1,2‐14C]trichloroacetic acid</topic><topic>Aliphatic compounds</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>one-pot synthesis</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bubner, M.</creatorcontrib><creatorcontrib>Fuksová, K.</creatorcontrib><creatorcontrib>Matucha, M.</creatorcontrib><creatorcontrib>Heise, K. 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H.</au><au>Bernhard, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of [1,2-14C]trichloroacetic acid</atitle><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle><addtitle>J Label Compd Radiopharm</addtitle><date>2001-10-15</date><risdate>2001</risdate><volume>44</volume><issue>11</issue><spage>811</spage><epage>814</epage><pages>811-814</pages><issn>0362-4803</issn><eissn>1099-1344</eissn><abstract>A growing interest in the phytotoxic effects of trichloroacetic acid (TCA) has led us to develop a small‐scale (<1 mmol) one‐pot synthesis of [1,2‐14C]TCA with >70% yield and specific activity of 3.7 GBq/mmol. Copyright © 2001 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/jlcr.505</doi><tpages>4</tpages></addata></record> |
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subjects | 2-14C]trichloroacetic acid [1,2‐14C]trichloroacetic acid Aliphatic compounds Chemistry Exact sciences and technology one-pot synthesis Organic chemistry Preparations and properties |
title | Synthesis of [1,2-14C]trichloroacetic acid |
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