Recent Development of Palladium-Supported Catalysts for Chemoselective Hydrogenation
This paper describes practical and selective hydrogenation methodologies using heterogeneous palladium catalysts. Chemoselectivity develops dependent on the catalyst activity based on the characteristic of the supports, derived from structural components, functional groups, and/or morphologies. We e...
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| Veröffentlicht in: | Chemical & pharmaceutical bulletin 2017/01/01, Vol.65(1), pp.2-9 |
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| container_title | Chemical & pharmaceutical bulletin |
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| creator | Monguchi, Yasunari Ichikawa, Tomohiro Sajiki, Hironao |
| description | This paper describes practical and selective hydrogenation methodologies using heterogeneous palladium catalysts. Chemoselectivity develops dependent on the catalyst activity based on the characteristic of the supports, derived from structural components, functional groups, and/or morphologies. We especially focus on our recent development of heterogeneous palladium catalysts supported on chelate resin, ceramic, and spherically shaped activated carbon. In addition, the application of flow technology for chemoselective hydrogenation using the palladium catalysts immobilized on molecular sieves 3A and boron nitride is outlined. |
| doi_str_mv | 10.1248/cpb.c16-00153 |
| format | Article |
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Chemoselectivity develops dependent on the catalyst activity based on the characteristic of the supports, derived from structural components, functional groups, and/or morphologies. We especially focus on our recent development of heterogeneous palladium catalysts supported on chelate resin, ceramic, and spherically shaped activated carbon. In addition, the application of flow technology for chemoselective hydrogenation using the palladium catalysts immobilized on molecular sieves 3A and boron nitride is outlined.</description><identifier>ISSN: 0009-2363</identifier><identifier>EISSN: 1347-5223</identifier><identifier>DOI: 10.1248/cpb.c16-00153</identifier><identifier>PMID: 28049910</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Activated carbon ; Boron ; Boron nitride ; Catalysis ; Catalysts ; Chelates ; chemoselectivity ; flow reaction ; Functional groups ; heterogeneous palladium catalyst ; Hydrogenation ; Molecular sieves ; Molecular Structure ; Morphology ; Oxidation ; Palladium ; Palladium - chemistry ; selective deprotection ; Stereoisomerism ; Structure-function relationships ; support ; Supports</subject><ispartof>Chemical and Pharmaceutical Bulletin, 2017/01/01, Vol.65(1), pp.2-9</ispartof><rights>2017 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c678t-b0b000634b751df6d623069332da87178bfcd17f9b5c0aaf3305d308a00368453</citedby><cites>FETCH-LOGICAL-c678t-b0b000634b751df6d623069332da87178bfcd17f9b5c0aaf3305d308a00368453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28049910$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Monguchi, Yasunari</creatorcontrib><creatorcontrib>Ichikawa, Tomohiro</creatorcontrib><creatorcontrib>Sajiki, Hironao</creatorcontrib><creatorcontrib>Gifu Pharmaceutical University</creatorcontrib><title>Recent Development of Palladium-Supported Catalysts for Chemoselective Hydrogenation</title><title>Chemical & pharmaceutical bulletin</title><addtitle>Chem. Pharm. Bull.</addtitle><description>This paper describes practical and selective hydrogenation methodologies using heterogeneous palladium catalysts. Chemoselectivity develops dependent on the catalyst activity based on the characteristic of the supports, derived from structural components, functional groups, and/or morphologies. We especially focus on our recent development of heterogeneous palladium catalysts supported on chelate resin, ceramic, and spherically shaped activated carbon. In addition, the application of flow technology for chemoselective hydrogenation using the palladium catalysts immobilized on molecular sieves 3A and boron nitride is outlined.</description><subject>Activated carbon</subject><subject>Boron</subject><subject>Boron nitride</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chelates</subject><subject>chemoselectivity</subject><subject>flow reaction</subject><subject>Functional groups</subject><subject>heterogeneous palladium catalyst</subject><subject>Hydrogenation</subject><subject>Molecular sieves</subject><subject>Molecular Structure</subject><subject>Morphology</subject><subject>Oxidation</subject><subject>Palladium</subject><subject>Palladium - chemistry</subject><subject>selective deprotection</subject><subject>Stereoisomerism</subject><subject>Structure-function relationships</subject><subject>support</subject><subject>Supports</subject><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkEFv1DAQhS0EokvhyBVF4sIlZWzHTnJEAVqkSiAoZ8uxJ21WThxsp9L-e7xN2UocPDPSfHrz_Ah5S-GCsqr5aJb-wlBZAlDBn5Ed5VVdCsb4c7IDgLZkXPIz8irGPQATUPOX5Iw1ULUthR25-YkG51R8xnt0fpmOsx-KH9o5bcd1Kn-ty-JDQlt0Oml3iCkWgw9Fd4eTj-jQpPEei6uDDf4WZ51GP78mLwbtIr557Ofk99cvN91Vef398lv36bo0sm5S2UOfHUpe9bWgdpBWMg6y5ZxZ3dS0bvrBWFoPbS8MaD1wDsJyaDQAl00l-Dn5sOkuwf9ZMSY1jdFgtj6jX6OijRC8opWgGX3_H7r3a5izO5Wzoo2sJDtS5UaZ4GMMOKgljJMOB0VBHeNWOW6V41YPcWf-3aPq2k9oT_S_fDNwuQF5Oxrt_OzGGZ9um1ibHOSoGNA6i0oBNDeW31baLJW_zLJStyntY9K3eDqlQxqNwwdjUih6LCeDT9s7HRTO_C9nHahi</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Monguchi, Yasunari</creator><creator>Ichikawa, Tomohiro</creator><creator>Sajiki, Hironao</creator><general>The Pharmaceutical Society of Japan</general><general>Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20170101</creationdate><title>Recent Development of Palladium-Supported Catalysts for Chemoselective Hydrogenation</title><author>Monguchi, Yasunari ; Ichikawa, Tomohiro ; Sajiki, Hironao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c678t-b0b000634b751df6d623069332da87178bfcd17f9b5c0aaf3305d308a00368453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Activated carbon</topic><topic>Boron</topic><topic>Boron nitride</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chelates</topic><topic>chemoselectivity</topic><topic>flow reaction</topic><topic>Functional groups</topic><topic>heterogeneous palladium catalyst</topic><topic>Hydrogenation</topic><topic>Molecular sieves</topic><topic>Molecular Structure</topic><topic>Morphology</topic><topic>Oxidation</topic><topic>Palladium</topic><topic>Palladium - chemistry</topic><topic>selective deprotection</topic><topic>Stereoisomerism</topic><topic>Structure-function relationships</topic><topic>support</topic><topic>Supports</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Monguchi, Yasunari</creatorcontrib><creatorcontrib>Ichikawa, Tomohiro</creatorcontrib><creatorcontrib>Sajiki, Hironao</creatorcontrib><creatorcontrib>Gifu Pharmaceutical University</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Monguchi, Yasunari</au><au>Ichikawa, Tomohiro</au><au>Sajiki, Hironao</au><aucorp>Gifu Pharmaceutical University</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent Development of Palladium-Supported Catalysts for Chemoselective Hydrogenation</atitle><jtitle>Chemical & pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>65</volume><issue>1</issue><spage>2</spage><epage>9</epage><pages>2-9</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><abstract>This paper describes practical and selective hydrogenation methodologies using heterogeneous palladium catalysts. Chemoselectivity develops dependent on the catalyst activity based on the characteristic of the supports, derived from structural components, functional groups, and/or morphologies. We especially focus on our recent development of heterogeneous palladium catalysts supported on chelate resin, ceramic, and spherically shaped activated carbon. 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| ispartof | Chemical and Pharmaceutical Bulletin, 2017/01/01, Vol.65(1), pp.2-9 |
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| language | eng |
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| source | MEDLINE; Free Full-Text Journals in Chemistry; EZB Electronic Journals Library; J-STAGE |
| subjects | Activated carbon Boron Boron nitride Catalysis Catalysts Chelates chemoselectivity flow reaction Functional groups heterogeneous palladium catalyst Hydrogenation Molecular sieves Molecular Structure Morphology Oxidation Palladium Palladium - chemistry selective deprotection Stereoisomerism Structure-function relationships support Supports |
| title | Recent Development of Palladium-Supported Catalysts for Chemoselective Hydrogenation |
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