When CuAAC 'Click Chemistry' goes heterogeneous
Within the green chemistry context, heterogeneous catalysis applied to organic synthesis is becoming an increasingly important field, bringing its own innovation and specific properties to organic chemistry. The well known 'click chemistry' is now challenged by this paradigm change and num...
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Veröffentlicht in: | Catalysis science & technology 2016-01, Vol.6 (4), p.923-957 |
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description | Within the green chemistry context, heterogeneous catalysis applied to organic synthesis is becoming an increasingly important field, bringing its own innovation and specific properties to organic chemistry. The well known 'click chemistry' is now challenged by this paradigm change and numerous methods involving heterogeneously catalyzed click chemistry have been and are currently being developed. This review covers these developments and shows that various reliable heterogeneous methods, alternative to the commonly used Meldal-Sharpless method, do exist for click chemistry, including those involving flow chemistry, and that they could be applied to a variety of compounds, solving some problems faced by more conventional methods.
Within the green chemistry context, heterogeneous catalysis is more and more applied to organic synthesis. The well known 'click chemistry' and especially its flagship, the copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC), is now catch up by such heterogenisation process and copper ions or metals have been grafted or deposited on or into various solids, such as (bio)polymers, charcoal, silica, zeolites, POM or MOF. |
doi_str_mv | 10.1039/c5cy01847a |
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Within the green chemistry context, heterogeneous catalysis is more and more applied to organic synthesis. The well known 'click chemistry' and especially its flagship, the copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC), is now catch up by such heterogenisation process and copper ions or metals have been grafted or deposited on or into various solids, such as (bio)polymers, charcoal, silica, zeolites, POM or MOF.</description><identifier>ISSN: 2044-4753</identifier><identifier>EISSN: 2044-4761</identifier><identifier>DOI: 10.1039/c5cy01847a</identifier><language>eng</language><subject>Catalysis ; Innovation ; Organic chemistry ; Synthesis (chemistry)</subject><ispartof>Catalysis science & technology, 2016-01, Vol.6 (4), p.923-957</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-f5b35d1e8bcf9c5b7766e3523da2d43b36e8a25c8fed4d1b86a423c582c6edad3</citedby><cites>FETCH-LOGICAL-c389t-f5b35d1e8bcf9c5b7766e3523da2d43b36e8a25c8fed4d1b86a423c582c6edad3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Chassaing, S</creatorcontrib><creatorcontrib>Bénéteau, V</creatorcontrib><creatorcontrib>Pale, P</creatorcontrib><title>When CuAAC 'Click Chemistry' goes heterogeneous</title><title>Catalysis science & technology</title><description>Within the green chemistry context, heterogeneous catalysis applied to organic synthesis is becoming an increasingly important field, bringing its own innovation and specific properties to organic chemistry. The well known 'click chemistry' is now challenged by this paradigm change and numerous methods involving heterogeneously catalyzed click chemistry have been and are currently being developed. This review covers these developments and shows that various reliable heterogeneous methods, alternative to the commonly used Meldal-Sharpless method, do exist for click chemistry, including those involving flow chemistry, and that they could be applied to a variety of compounds, solving some problems faced by more conventional methods.
Within the green chemistry context, heterogeneous catalysis is more and more applied to organic synthesis. The well known 'click chemistry' and especially its flagship, the copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC), is now catch up by such heterogenisation process and copper ions or metals have been grafted or deposited on or into various solids, such as (bio)polymers, charcoal, silica, zeolites, POM or MOF.</description><subject>Catalysis</subject><subject>Innovation</subject><subject>Organic chemistry</subject><subject>Synthesis (chemistry)</subject><issn>2044-4753</issn><issn>2044-4761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpFkE1Lw0AQhhdRsNRevAu5VYTY_c7mGBarQsGLIp7CZnfSRNOm7iaH_HtjI3UuM4eHl3cehK4JvieYpSsr7ICJ4ok5QzOKOY95Isn56RbsEi1C-MTj8JRgRWdo9V7BPtJ9luloqZvafkW6gl0dOj8so20LIaqgA99uYQ9tH67QRWmaAIu_PUdv64dX_RRvXh6fdbaJLVNpF5eiYMIRUIUtUyuKJJESmKDMGeo4K5gEZaiwqgTHHSmUNJwyKxS1EpxxbI5up9yDb797CF0-drLQNOZYIydq_EEkgosRvZtQ69sQPJT5wdc744ec4PxXTK6F_jiKyUb4ZoJ9sCfuXxz7AQjKXiQ</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Chassaing, S</creator><creator>Bénéteau, V</creator><creator>Pale, P</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20160101</creationdate><title>When CuAAC 'Click Chemistry' goes heterogeneous</title><author>Chassaing, S ; Bénéteau, V ; Pale, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-f5b35d1e8bcf9c5b7766e3523da2d43b36e8a25c8fed4d1b86a423c582c6edad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Catalysis</topic><topic>Innovation</topic><topic>Organic chemistry</topic><topic>Synthesis (chemistry)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chassaing, S</creatorcontrib><creatorcontrib>Bénéteau, V</creatorcontrib><creatorcontrib>Pale, P</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Catalysis science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chassaing, S</au><au>Bénéteau, V</au><au>Pale, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>When CuAAC 'Click Chemistry' goes heterogeneous</atitle><jtitle>Catalysis science & technology</jtitle><date>2016-01-01</date><risdate>2016</risdate><volume>6</volume><issue>4</issue><spage>923</spage><epage>957</epage><pages>923-957</pages><issn>2044-4753</issn><eissn>2044-4761</eissn><abstract>Within the green chemistry context, heterogeneous catalysis applied to organic synthesis is becoming an increasingly important field, bringing its own innovation and specific properties to organic chemistry. The well known 'click chemistry' is now challenged by this paradigm change and numerous methods involving heterogeneously catalyzed click chemistry have been and are currently being developed. This review covers these developments and shows that various reliable heterogeneous methods, alternative to the commonly used Meldal-Sharpless method, do exist for click chemistry, including those involving flow chemistry, and that they could be applied to a variety of compounds, solving some problems faced by more conventional methods.
Within the green chemistry context, heterogeneous catalysis is more and more applied to organic synthesis. The well known 'click chemistry' and especially its flagship, the copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC), is now catch up by such heterogenisation process and copper ions or metals have been grafted or deposited on or into various solids, such as (bio)polymers, charcoal, silica, zeolites, POM or MOF.</abstract><doi>10.1039/c5cy01847a</doi><tpages>35</tpages></addata></record> |
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title | When CuAAC 'Click Chemistry' goes heterogeneous |
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