Development of porphyrin syntheses
Hans Fischer (Munich, Germany) and S. Fergus MacDonald (Ottawa, Canada) devised efficient porphyrin syntheses based on condensation reactions of dipyrromethenes (Fischer) or dipyrromethanes (MacDonald). These historically significant processes and subsequent developments are discussed, along with mo...
Gespeichert in:
| Veröffentlicht in: | New journal of chemistry 2016, Vol.4 (7), p.5644-5649 |
|---|---|
| 1. Verfasser: | |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 5649 |
|---|---|
| container_issue | 7 |
| container_start_page | 5644 |
| container_title | New journal of chemistry |
| container_volume | 4 |
| creator | Smith, Kevin M |
| description | Hans Fischer (Munich, Germany) and S. Fergus MacDonald (Ottawa, Canada) devised efficient porphyrin syntheses based on condensation reactions of dipyrromethenes (Fischer) or dipyrromethanes (MacDonald). These historically significant processes and subsequent developments are discussed, along with monopyrrole tetramerizations that give 5,10,15,20-tetra-arylporphyrins, to show that the art of porphyrin synthesis continues to flourish.
Personal historical comments relating to the advancement of porphyrin syntheses using monopyrroles, dipyrroles, and open-chain tetrapyrroles are presented. |
| doi_str_mv | 10.1039/c6nj00820h |
| format | Article |
| fullrecord | <record><control><sourceid>rsc_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1039_C6NJ00820H</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c6nj00820h</sourcerecordid><originalsourceid>FETCH-LOGICAL-c319t-355bba83b8795a016983a9507bbcb49708f7344cbb3bdbf291bfce87027c4d0a3</originalsourceid><addsrcrecordid>eNpFz01Lw0AQh_FFFKzVi3cheBSiM9nNvhwlvrSl6EXPYWe7SyptEnaDkG9vtKKnmcOPPzyMXSLcInBz52T7AaALaI7YDLk0uSkkHk8_CpFDKeQpO0tpMohK4oxdP_hPv-v6vW-HrAtZ38W-GeO2zdLYDo1PPp2zk2B3yV_83jl7f3p8qxb5-vV5Wd2vc8fRDDkvSyKrOWllSgsojebWlKCIHAmjQAfFhXBEnDYUCoMUnNcKCuXEBiyfs5vDrotdStGHuo_bvY1jjVB_19WVfFn91C0mfHXAMbk_91_PvwCPeUus</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Development of porphyrin syntheses</title><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>Smith, Kevin M</creator><creatorcontrib>Smith, Kevin M</creatorcontrib><description>Hans Fischer (Munich, Germany) and S. Fergus MacDonald (Ottawa, Canada) devised efficient porphyrin syntheses based on condensation reactions of dipyrromethenes (Fischer) or dipyrromethanes (MacDonald). These historically significant processes and subsequent developments are discussed, along with monopyrrole tetramerizations that give 5,10,15,20-tetra-arylporphyrins, to show that the art of porphyrin synthesis continues to flourish.
Personal historical comments relating to the advancement of porphyrin syntheses using monopyrroles, dipyrroles, and open-chain tetrapyrroles are presented.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/c6nj00820h</identifier><language>eng</language><ispartof>New journal of chemistry, 2016, Vol.4 (7), p.5644-5649</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-355bba83b8795a016983a9507bbcb49708f7344cbb3bdbf291bfce87027c4d0a3</citedby><cites>FETCH-LOGICAL-c319t-355bba83b8795a016983a9507bbcb49708f7344cbb3bdbf291bfce87027c4d0a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids></links><search><creatorcontrib>Smith, Kevin M</creatorcontrib><title>Development of porphyrin syntheses</title><title>New journal of chemistry</title><description>Hans Fischer (Munich, Germany) and S. Fergus MacDonald (Ottawa, Canada) devised efficient porphyrin syntheses based on condensation reactions of dipyrromethenes (Fischer) or dipyrromethanes (MacDonald). These historically significant processes and subsequent developments are discussed, along with monopyrrole tetramerizations that give 5,10,15,20-tetra-arylporphyrins, to show that the art of porphyrin synthesis continues to flourish.
Personal historical comments relating to the advancement of porphyrin syntheses using monopyrroles, dipyrroles, and open-chain tetrapyrroles are presented.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpFz01Lw0AQh_FFFKzVi3cheBSiM9nNvhwlvrSl6EXPYWe7SyptEnaDkG9vtKKnmcOPPzyMXSLcInBz52T7AaALaI7YDLk0uSkkHk8_CpFDKeQpO0tpMohK4oxdP_hPv-v6vW-HrAtZ38W-GeO2zdLYDo1PPp2zk2B3yV_83jl7f3p8qxb5-vV5Wd2vc8fRDDkvSyKrOWllSgsojebWlKCIHAmjQAfFhXBEnDYUCoMUnNcKCuXEBiyfs5vDrotdStGHuo_bvY1jjVB_19WVfFn91C0mfHXAMbk_91_PvwCPeUus</recordid><startdate>2016</startdate><enddate>2016</enddate><creator>Smith, Kevin M</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2016</creationdate><title>Development of porphyrin syntheses</title><author>Smith, Kevin M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-355bba83b8795a016983a9507bbcb49708f7344cbb3bdbf291bfce87027c4d0a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Kevin M</creatorcontrib><collection>CrossRef</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Kevin M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of porphyrin syntheses</atitle><jtitle>New journal of chemistry</jtitle><date>2016</date><risdate>2016</risdate><volume>4</volume><issue>7</issue><spage>5644</spage><epage>5649</epage><pages>5644-5649</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>Hans Fischer (Munich, Germany) and S. Fergus MacDonald (Ottawa, Canada) devised efficient porphyrin syntheses based on condensation reactions of dipyrromethenes (Fischer) or dipyrromethanes (MacDonald). These historically significant processes and subsequent developments are discussed, along with monopyrrole tetramerizations that give 5,10,15,20-tetra-arylporphyrins, to show that the art of porphyrin synthesis continues to flourish.
Personal historical comments relating to the advancement of porphyrin syntheses using monopyrroles, dipyrroles, and open-chain tetrapyrroles are presented.</abstract><doi>10.1039/c6nj00820h</doi><tpages>6</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1144-0546 |
| ispartof | New journal of chemistry, 2016, Vol.4 (7), p.5644-5649 |
| issn | 1144-0546 1369-9261 |
| language | eng |
| recordid | cdi_crossref_primary_10_1039_C6NJ00820H |
| source | Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
| title | Development of porphyrin syntheses |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T14%3A04%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Development%20of%20porphyrin%20syntheses&rft.jtitle=New%20journal%20of%20chemistry&rft.au=Smith,%20Kevin%20M&rft.date=2016&rft.volume=4&rft.issue=7&rft.spage=5644&rft.epage=5649&rft.pages=5644-5649&rft.issn=1144-0546&rft.eissn=1369-9261&rft_id=info:doi/10.1039/c6nj00820h&rft_dat=%3Crsc_cross%3Ec6nj00820h%3C/rsc_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |