Synthesis of Angular Polycyclic Aromatic Hydrocarbons Via Ti(IV)-Promoted Aldol-Type Condensation of Silyl Enol Ethers with 2-Arylacetaldehydes
A novel one-pot synthesis of angular polycyclic hydrocarbon ring systems is described. The method involves Ti(IV)-promoted aldol-type condensation of silyl enol ethers with 2-arylacetaldehydes with concurrent cyclization and double dehydration of the adducts. Dehydrogenation of the partially saturat...
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Veröffentlicht in: | Polycyclic aromatic compounds 1991-01, Vol.2 (1), p.1-11 |
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creator | Raddo, Pasquale Di Hahn, Jung-Tai Harvey, Ronald G. |
description | A novel one-pot synthesis of angular polycyclic hydrocarbon ring systems is described. The method involves Ti(IV)-promoted aldol-type condensation of silyl enol ethers with 2-arylacetaldehydes with concurrent cyclization and double dehydration of the adducts. Dehydrogenation of the partially saturated polyarene products either catalytically over palladium or with quinone oxidants, such as DDQ, affords fully aromatic polycyclic hydrocarbons. Examples of the synthesis of various phenanthrene, chrysene, benz[a]anthracene, and benz[j]acephenanthrylene derivatives via this route are presented. |
doi_str_mv | 10.1080/10406639108047852 |
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The method involves Ti(IV)-promoted aldol-type condensation of silyl enol ethers with 2-arylacetaldehydes with concurrent cyclization and double dehydration of the adducts. Dehydrogenation of the partially saturated polyarene products either catalytically over palladium or with quinone oxidants, such as DDQ, affords fully aromatic polycyclic hydrocarbons. Examples of the synthesis of various phenanthrene, chrysene, benz[a]anthracene, and benz[j]acephenanthrylene derivatives via this route are presented.</description><identifier>ISSN: 1040-6638</identifier><identifier>EISSN: 1563-5333</identifier><identifier>DOI: 10.1080/10406639108047852</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><subject>5-methylchrysene ; angular polycyclic hydrocarbons ; benz[a]anthracene ; benz[j]aceanthrylene ; chrysene ; synthesis</subject><ispartof>Polycyclic aromatic compounds, 1991-01, Vol.2 (1), p.1-11</ispartof><rights>Copyright Taylor & Francis Group, LLC 1991</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c213t-db1a38138fcb5a494f72847b0c7006b4e67214ff30dc4b1ad2971e2a0fa09f623</citedby><cites>FETCH-LOGICAL-c213t-db1a38138fcb5a494f72847b0c7006b4e67214ff30dc4b1ad2971e2a0fa09f623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/10406639108047852$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/10406639108047852$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,59620,60409</link.rule.ids></links><search><creatorcontrib>Raddo, Pasquale Di</creatorcontrib><creatorcontrib>Hahn, Jung-Tai</creatorcontrib><creatorcontrib>Harvey, Ronald G.</creatorcontrib><title>Synthesis of Angular Polycyclic Aromatic Hydrocarbons Via Ti(IV)-Promoted Aldol-Type Condensation of Silyl Enol Ethers with 2-Arylacetaldehydes</title><title>Polycyclic aromatic compounds</title><description>A novel one-pot synthesis of angular polycyclic hydrocarbon ring systems is described. The method involves Ti(IV)-promoted aldol-type condensation of silyl enol ethers with 2-arylacetaldehydes with concurrent cyclization and double dehydration of the adducts. Dehydrogenation of the partially saturated polyarene products either catalytically over palladium or with quinone oxidants, such as DDQ, affords fully aromatic polycyclic hydrocarbons. Examples of the synthesis of various phenanthrene, chrysene, benz[a]anthracene, and benz[j]acephenanthrylene derivatives via this route are presented.</description><subject>5-methylchrysene</subject><subject>angular polycyclic hydrocarbons</subject><subject>benz[a]anthracene</subject><subject>benz[j]aceanthrylene</subject><subject>chrysene</subject><subject>synthesis</subject><issn>1040-6638</issn><issn>1563-5333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKAzEUhgdRsFYfwF2WuhjNrZkZcDOUagsFC63dDplcbCRNSjJS8hS-sim6Ezfnwvm__8BfFLcIPiBYw0cEKWSMNKeFVvUEnxUjNGGknBBCzvOc72UW1JfFVYwfEGLEGB4VX-vkhp2KJgKvQevePy0PYOVtEklYI0Ab_J4PeZgnGbzgofcugq3hYGPuFtv7cpUFflAStFZ6W27SQYGpd1K5mDnvTr5rY5MFM-dzyd9CBEcz7AAu25AsF2rgVqpdkipeFxea26hufvu4eHuebabzcvn6spi2y1JgRIZS9oiTGpFai37CaUN1hWta9VBUELKeKlZhRLUmUAqatRI3FVKYQ81hoxkm4wL9-IrgYwxKd4dg9jykDsHuFGL3J9HMPP0wxmkf9vzog5XdwJP1QQfuhIkd-R__BsuufWU</recordid><startdate>19910101</startdate><enddate>19910101</enddate><creator>Raddo, Pasquale Di</creator><creator>Hahn, Jung-Tai</creator><creator>Harvey, Ronald G.</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19910101</creationdate><title>Synthesis of Angular Polycyclic Aromatic Hydrocarbons Via Ti(IV)-Promoted Aldol-Type Condensation of Silyl Enol Ethers with 2-Arylacetaldehydes</title><author>Raddo, Pasquale Di ; Hahn, Jung-Tai ; Harvey, Ronald G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c213t-db1a38138fcb5a494f72847b0c7006b4e67214ff30dc4b1ad2971e2a0fa09f623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>5-methylchrysene</topic><topic>angular polycyclic hydrocarbons</topic><topic>benz[a]anthracene</topic><topic>benz[j]aceanthrylene</topic><topic>chrysene</topic><topic>synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raddo, Pasquale Di</creatorcontrib><creatorcontrib>Hahn, Jung-Tai</creatorcontrib><creatorcontrib>Harvey, Ronald G.</creatorcontrib><collection>CrossRef</collection><jtitle>Polycyclic aromatic compounds</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raddo, Pasquale Di</au><au>Hahn, Jung-Tai</au><au>Harvey, Ronald G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Angular Polycyclic Aromatic Hydrocarbons Via Ti(IV)-Promoted Aldol-Type Condensation of Silyl Enol Ethers with 2-Arylacetaldehydes</atitle><jtitle>Polycyclic aromatic compounds</jtitle><date>1991-01-01</date><risdate>1991</risdate><volume>2</volume><issue>1</issue><spage>1</spage><epage>11</epage><pages>1-11</pages><issn>1040-6638</issn><eissn>1563-5333</eissn><abstract>A novel one-pot synthesis of angular polycyclic hydrocarbon ring systems is described. The method involves Ti(IV)-promoted aldol-type condensation of silyl enol ethers with 2-arylacetaldehydes with concurrent cyclization and double dehydration of the adducts. Dehydrogenation of the partially saturated polyarene products either catalytically over palladium or with quinone oxidants, such as DDQ, affords fully aromatic polycyclic hydrocarbons. Examples of the synthesis of various phenanthrene, chrysene, benz[a]anthracene, and benz[j]acephenanthrylene derivatives via this route are presented.</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/10406639108047852</doi><tpages>11</tpages></addata></record> |
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subjects | 5-methylchrysene angular polycyclic hydrocarbons benz[a]anthracene benz[j]aceanthrylene chrysene synthesis |
title | Synthesis of Angular Polycyclic Aromatic Hydrocarbons Via Ti(IV)-Promoted Aldol-Type Condensation of Silyl Enol Ethers with 2-Arylacetaldehydes |
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