ChemInform Abstract: Catalyst‐Free Three‐Component Tandem CDC Cyclization: Convenient Access to Isoindolinones from Aromatic Acid, Amides, and DMSO by a Pummerer‐Type Rearrangement
A catalyst free three‐component reaction of 3,4,5‐trimethoxybenzoic acid with sulfonamides or carboxylic amides and DMSO as methylene source proceeds through a Pummerer‐type rearrangement to provide a convenient access to N‐substituted isoindolinones.
Gespeichert in:
| Veröffentlicht in: | ChemInform 2016-08, Vol.47 (36), p.no-no |
|---|---|
| Hauptverfasser: | , , , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | no |
|---|---|
| container_issue | 36 |
| container_start_page | no |
| container_title | ChemInform |
| container_volume | 47 |
| creator | Wang, Peng‐Min Pu, Fan Liu, Ke‐Yan Li, Chao‐Jun Liu, Zhong‐Wen Shi, Xian‐Ying Fan, Juan Yang, Ming‐Yu Wei, Jun‐Fa |
| description | A catalyst free three‐component reaction of 3,4,5‐trimethoxybenzoic acid with sulfonamides or carboxylic amides and DMSO as methylene source proceeds through a Pummerer‐type rearrangement to provide a convenient access to N‐substituted isoindolinones. |
| doi_str_mv | 10.1002/chin.201636116 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1813202343</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4155775561</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1176-4f2b0dfd2ef5cc34c9833d6d5614ec7c01db19bcc51d6959e8e41a9f43a9a0543</originalsourceid><addsrcrecordid>eNqFkc1uEzEURi0EEqGwZW2JbSf1z4wnZhe5LY1UKIKwHnnsO8TV2A72BDSs-gg8D4_Dk-AoCJZsrmXpnPtJ90PoJSVLSgi7MDsXloxQwQWl4hFa0IaxignRPkYLIjmt2ka2T9GznO8Lz9sVW6Cfagd-E4aYPF73eUraTK-x0pMe5zz9evhxnQDwdldm-ajo9zFAmPBWBwseq0uF1WxG911PLoZixvAVgjsia2MgZzxFvMnRBRtHF4qc8ZBiCSujOKZgzp7jtXcW8jkua_Hl2493uJ-xxu8P3kOCVKK38x7wB9Ap6fAZfAl4jp4Meszw4s97hj5dX23VTXV792aj1reVobQVVT2wntjBMhgaY3ht5IpzK2wjaA2mNYTansremIZaIRsJK6iplkPNtdSkqfkZenXau0_xywHy1N3HQwolsqMrylk5Zc0LtTxRJsWcEwzdPjmv09xR0h376Y79dH_7KYI8Cd_cCPN_6E7dbN79c38D-qmZ4A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1813202343</pqid></control><display><type>article</type><title>ChemInform Abstract: Catalyst‐Free Three‐Component Tandem CDC Cyclization: Convenient Access to Isoindolinones from Aromatic Acid, Amides, and DMSO by a Pummerer‐Type Rearrangement</title><source>Access via Wiley Online Library</source><creator>Wang, Peng‐Min ; Pu, Fan ; Liu, Ke‐Yan ; Li, Chao‐Jun ; Liu, Zhong‐Wen ; Shi, Xian‐Ying ; Fan, Juan ; Yang, Ming‐Yu ; Wei, Jun‐Fa</creator><creatorcontrib>Wang, Peng‐Min ; Pu, Fan ; Liu, Ke‐Yan ; Li, Chao‐Jun ; Liu, Zhong‐Wen ; Shi, Xian‐Ying ; Fan, Juan ; Yang, Ming‐Yu ; Wei, Jun‐Fa</creatorcontrib><description>A catalyst free three‐component reaction of 3,4,5‐trimethoxybenzoic acid with sulfonamides or carboxylic amides and DMSO as methylene source proceeds through a Pummerer‐type rearrangement to provide a convenient access to N‐substituted isoindolinones.</description><identifier>ISSN: 0931-7597</identifier><identifier>EISSN: 1522-2667</identifier><identifier>DOI: 10.1002/chin.201636116</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag</publisher><subject>indole derivatives, isoindole derivatives ; rearrangements ; ring closure reactions, annulation reactions</subject><ispartof>ChemInform, 2016-08, Vol.47 (36), p.no-no</ispartof><rights>2016 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><rights>2016 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1176-4f2b0dfd2ef5cc34c9833d6d5614ec7c01db19bcc51d6959e8e41a9f43a9a0543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchin.201636116$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchin.201636116$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Wang, Peng‐Min</creatorcontrib><creatorcontrib>Pu, Fan</creatorcontrib><creatorcontrib>Liu, Ke‐Yan</creatorcontrib><creatorcontrib>Li, Chao‐Jun</creatorcontrib><creatorcontrib>Liu, Zhong‐Wen</creatorcontrib><creatorcontrib>Shi, Xian‐Ying</creatorcontrib><creatorcontrib>Fan, Juan</creatorcontrib><creatorcontrib>Yang, Ming‐Yu</creatorcontrib><creatorcontrib>Wei, Jun‐Fa</creatorcontrib><title>ChemInform Abstract: Catalyst‐Free Three‐Component Tandem CDC Cyclization: Convenient Access to Isoindolinones from Aromatic Acid, Amides, and DMSO by a Pummerer‐Type Rearrangement</title><title>ChemInform</title><description>A catalyst free three‐component reaction of 3,4,5‐trimethoxybenzoic acid with sulfonamides or carboxylic amides and DMSO as methylene source proceeds through a Pummerer‐type rearrangement to provide a convenient access to N‐substituted isoindolinones.</description><subject>indole derivatives, isoindole derivatives</subject><subject>rearrangements</subject><subject>ring closure reactions, annulation reactions</subject><issn>0931-7597</issn><issn>1522-2667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkc1uEzEURi0EEqGwZW2JbSf1z4wnZhe5LY1UKIKwHnnsO8TV2A72BDSs-gg8D4_Dk-AoCJZsrmXpnPtJ90PoJSVLSgi7MDsXloxQwQWl4hFa0IaxignRPkYLIjmt2ka2T9GznO8Lz9sVW6Cfagd-E4aYPF73eUraTK-x0pMe5zz9evhxnQDwdldm-ajo9zFAmPBWBwseq0uF1WxG911PLoZixvAVgjsia2MgZzxFvMnRBRtHF4qc8ZBiCSujOKZgzp7jtXcW8jkua_Hl2493uJ-xxu8P3kOCVKK38x7wB9Ap6fAZfAl4jp4Meszw4s97hj5dX23VTXV792aj1reVobQVVT2wntjBMhgaY3ht5IpzK2wjaA2mNYTansremIZaIRsJK6iplkPNtdSkqfkZenXau0_xywHy1N3HQwolsqMrylk5Zc0LtTxRJsWcEwzdPjmv09xR0h376Y79dH_7KYI8Cd_cCPN_6E7dbN79c38D-qmZ4A</recordid><startdate>201608</startdate><enddate>201608</enddate><creator>Wang, Peng‐Min</creator><creator>Pu, Fan</creator><creator>Liu, Ke‐Yan</creator><creator>Li, Chao‐Jun</creator><creator>Liu, Zhong‐Wen</creator><creator>Shi, Xian‐Ying</creator><creator>Fan, Juan</creator><creator>Yang, Ming‐Yu</creator><creator>Wei, Jun‐Fa</creator><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201608</creationdate><title>ChemInform Abstract: Catalyst‐Free Three‐Component Tandem CDC Cyclization: Convenient Access to Isoindolinones from Aromatic Acid, Amides, and DMSO by a Pummerer‐Type Rearrangement</title><author>Wang, Peng‐Min ; Pu, Fan ; Liu, Ke‐Yan ; Li, Chao‐Jun ; Liu, Zhong‐Wen ; Shi, Xian‐Ying ; Fan, Juan ; Yang, Ming‐Yu ; Wei, Jun‐Fa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1176-4f2b0dfd2ef5cc34c9833d6d5614ec7c01db19bcc51d6959e8e41a9f43a9a0543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>indole derivatives, isoindole derivatives</topic><topic>rearrangements</topic><topic>ring closure reactions, annulation reactions</topic><toplevel>online_resources</toplevel><creatorcontrib>Wang, Peng‐Min</creatorcontrib><creatorcontrib>Pu, Fan</creatorcontrib><creatorcontrib>Liu, Ke‐Yan</creatorcontrib><creatorcontrib>Li, Chao‐Jun</creatorcontrib><creatorcontrib>Liu, Zhong‐Wen</creatorcontrib><creatorcontrib>Shi, Xian‐Ying</creatorcontrib><creatorcontrib>Fan, Juan</creatorcontrib><creatorcontrib>Yang, Ming‐Yu</creatorcontrib><creatorcontrib>Wei, Jun‐Fa</creatorcontrib><collection>CrossRef</collection><jtitle>ChemInform</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Peng‐Min</au><au>Pu, Fan</au><au>Liu, Ke‐Yan</au><au>Li, Chao‐Jun</au><au>Liu, Zhong‐Wen</au><au>Shi, Xian‐Ying</au><au>Fan, Juan</au><au>Yang, Ming‐Yu</au><au>Wei, Jun‐Fa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChemInform Abstract: Catalyst‐Free Three‐Component Tandem CDC Cyclization: Convenient Access to Isoindolinones from Aromatic Acid, Amides, and DMSO by a Pummerer‐Type Rearrangement</atitle><jtitle>ChemInform</jtitle><date>2016-08</date><risdate>2016</risdate><volume>47</volume><issue>36</issue><spage>no</spage><epage>no</epage><pages>no-no</pages><issn>0931-7597</issn><eissn>1522-2667</eissn><abstract>A catalyst free three‐component reaction of 3,4,5‐trimethoxybenzoic acid with sulfonamides or carboxylic amides and DMSO as methylene source proceeds through a Pummerer‐type rearrangement to provide a convenient access to N‐substituted isoindolinones.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag</pub><doi>10.1002/chin.201636116</doi><tpages>1</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0931-7597 |
| ispartof | ChemInform, 2016-08, Vol.47 (36), p.no-no |
| issn | 0931-7597 1522-2667 |
| language | eng |
| recordid | cdi_proquest_journals_1813202343 |
| source | Access via Wiley Online Library |
| subjects | indole derivatives, isoindole derivatives rearrangements ring closure reactions, annulation reactions |
| title | ChemInform Abstract: Catalyst‐Free Three‐Component Tandem CDC Cyclization: Convenient Access to Isoindolinones from Aromatic Acid, Amides, and DMSO by a Pummerer‐Type Rearrangement |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T07%3A17%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ChemInform%20Abstract:%20Catalyst%E2%80%90Free%20Three%E2%80%90Component%20Tandem%20CDC%20Cyclization:%20Convenient%20Access%20to%20Isoindolinones%20from%20Aromatic%20Acid,%20Amides,%20and%20DMSO%20by%20a%20Pummerer%E2%80%90Type%20Rearrangement&rft.jtitle=ChemInform&rft.au=Wang,%20Peng%E2%80%90Min&rft.date=2016-08&rft.volume=47&rft.issue=36&rft.spage=no&rft.epage=no&rft.pages=no-no&rft.issn=0931-7597&rft.eissn=1522-2667&rft_id=info:doi/10.1002/chin.201636116&rft_dat=%3Cproquest_cross%3E4155775561%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1813202343&rft_id=info:pmid/&rfr_iscdi=true |