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Construction of Multifunctionalized Azopyrazoles by Silver- Catalyzed Cascade Reaction of Diazo Compounds
A variety of multisubstituted azopyrazoles were synthesized in good yield from an efficient one‐pot silver trifluoromethanesulfonate (AgOTf)‐catalyzed cascade reaction of α‐diazo‐β‐keto esters with two arylhydrazines or two arylhydrazine hydrochlorides. This cascade reaction included pyrazolone form...
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Published in: | Advanced synthesis & catalysis 2015-08, Vol.357 (12), p.2657-2664 |
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container_title | Advanced synthesis & catalysis |
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creator | Pandit, Rameshwar Prasad Lee, Yong Rok |
description | A variety of multisubstituted azopyrazoles were synthesized in good yield from an efficient one‐pot silver trifluoromethanesulfonate (AgOTf)‐catalyzed cascade reaction of α‐diazo‐β‐keto esters with two arylhydrazines or two arylhydrazine hydrochlorides. This cascade reaction included pyrazolone formation, NH insertion, and oxidation. For the synthesis of more diverse azopyrazoles bearing two different aromatic rings, the silver(I)‐catalyzed cascade reaction of 4‐diazopyrazol‐3‐one with arylhydrazine hydrochlorides was also developed. The advantages of these methodologies are easy handling, mild reaction conditions, and an effective and non‐toxic catalyst usage. |
doi_str_mv | 10.1002/adsc.201500197 |
format | article |
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This cascade reaction included pyrazolone formation, NH insertion, and oxidation. For the synthesis of more diverse azopyrazoles bearing two different aromatic rings, the silver(I)‐catalyzed cascade reaction of 4‐diazopyrazol‐3‐one with arylhydrazine hydrochlorides was also developed. The advantages of these methodologies are easy handling, mild reaction conditions, and an effective and non‐toxic catalyst usage.</description><identifier>ISSN: 1615-4150</identifier><identifier>EISSN: 1615-4169</identifier><identifier>DOI: 10.1002/adsc.201500197</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>activation ; Aromatic compounds ; Bearing ; Cascades ; coupling ; Esters ; ethers ; Hydrochlorides ; Insertion ; multifunctionalized azopyrazoles ; palladium ; Pyrazolones ; radicals ; Synthesis</subject><ispartof>Advanced synthesis & catalysis, 2015-08, Vol.357 (12), p.2657-2664</ispartof><rights>2015 WILEY‐VCH Verlag GmbH & Co. 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Catal</addtitle><description>A variety of multisubstituted azopyrazoles were synthesized in good yield from an efficient one‐pot silver trifluoromethanesulfonate (AgOTf)‐catalyzed cascade reaction of α‐diazo‐β‐keto esters with two arylhydrazines or two arylhydrazine hydrochlorides. This cascade reaction included pyrazolone formation, NH insertion, and oxidation. For the synthesis of more diverse azopyrazoles bearing two different aromatic rings, the silver(I)‐catalyzed cascade reaction of 4‐diazopyrazol‐3‐one with arylhydrazine hydrochlorides was also developed. The advantages of these methodologies are easy handling, mild reaction conditions, and an effective and non‐toxic catalyst usage.</description><subject>activation</subject><subject>Aromatic compounds</subject><subject>Bearing</subject><subject>Cascades</subject><subject>coupling</subject><subject>Esters</subject><subject>ethers</subject><subject>Hydrochlorides</subject><subject>Insertion</subject><subject>multifunctionalized azopyrazoles</subject><subject>palladium</subject><subject>Pyrazolones</subject><subject>radicals</subject><subject>Synthesis</subject><issn>1615-4150</issn><issn>1615-4169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAURSMEEqWwMmdkSXmuk7gZSwoFqYBE-Rgtx3mWDG5c7ARIfz0pRREb07t6OucONwhOCYwIwPhclF6OxkASAJKxvWBAUpJEMUmz_T4ncBgcef_aIWzC2CDQua187RpZa1uFVoW3jam1aqqfhzB6g2U43dh168TGGvRh0YZLbT7QRWEuamHaLZELL0WJ4QOKvmmmOyPM7Wptm6r0x8GBEsbjye8dBk9Xl4_5dbS4n9_k00UkacZYlJRZkVEmYykoK1CVKAFYmqqYyHFKgUkQSrEMgUIqhKIUCywYLbGAtGAFHQZnu961s-8N-pqvtJdojKjQNp4TRgEmJI6hQ0c7VDrrvUPF106vhGs5Ab7dlG835f2mnZDthE9tsP2H5tPZMv_rRjtX-xq_ele4N54yyhL-cjfn8eTieZHlY07oN2ohjI4</recordid><startdate>20150824</startdate><enddate>20150824</enddate><creator>Pandit, Rameshwar Prasad</creator><creator>Lee, Yong Rok</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20150824</creationdate><title>Construction of Multifunctionalized Azopyrazoles by Silver- Catalyzed Cascade Reaction of Diazo Compounds</title><author>Pandit, Rameshwar Prasad ; Lee, Yong Rok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3977-5d9b937c4ca37befdec00766f41c26307c0aff79e0306aaf33ebeb73deb06b7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>activation</topic><topic>Aromatic compounds</topic><topic>Bearing</topic><topic>Cascades</topic><topic>coupling</topic><topic>Esters</topic><topic>ethers</topic><topic>Hydrochlorides</topic><topic>Insertion</topic><topic>multifunctionalized azopyrazoles</topic><topic>palladium</topic><topic>Pyrazolones</topic><topic>radicals</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pandit, Rameshwar Prasad</creatorcontrib><creatorcontrib>Lee, Yong Rok</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced synthesis & catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pandit, Rameshwar Prasad</au><au>Lee, Yong Rok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction of Multifunctionalized Azopyrazoles by Silver- Catalyzed Cascade Reaction of Diazo Compounds</atitle><jtitle>Advanced synthesis & catalysis</jtitle><addtitle>Adv. Synth. Catal</addtitle><date>2015-08-24</date><risdate>2015</risdate><volume>357</volume><issue>12</issue><spage>2657</spage><epage>2664</epage><pages>2657-2664</pages><issn>1615-4150</issn><eissn>1615-4169</eissn><abstract>A variety of multisubstituted azopyrazoles were synthesized in good yield from an efficient one‐pot silver trifluoromethanesulfonate (AgOTf)‐catalyzed cascade reaction of α‐diazo‐β‐keto esters with two arylhydrazines or two arylhydrazine hydrochlorides. This cascade reaction included pyrazolone formation, NH insertion, and oxidation. For the synthesis of more diverse azopyrazoles bearing two different aromatic rings, the silver(I)‐catalyzed cascade reaction of 4‐diazopyrazol‐3‐one with arylhydrazine hydrochlorides was also developed. 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subjects | activation Aromatic compounds Bearing Cascades coupling Esters ethers Hydrochlorides Insertion multifunctionalized azopyrazoles palladium Pyrazolones radicals Synthesis |
title | Construction of Multifunctionalized Azopyrazoles by Silver- Catalyzed Cascade Reaction of Diazo Compounds |
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