Cover Feature: An Improved Protocol for the Morita‐Baylis‐Hillman Reaction Allows Unprecedented Broad Synthetic Scope (Eur. J. Org. Chem. 9/2022)
The Cover Feature illustrates the effect of acetic acid on the rate of the Morita–Baylis–Hillman reaction. The use of acetic acid as a fuel (additive) increases the reaction rate in all tested cases, with special emphasis on electron‐rich electrophilic partners. We believe that a general acid cataly...
Gespeichert in:
| Veröffentlicht in: | European journal of organic chemistry 2022-03, Vol.2022 (9), p.n/a |
|---|---|
| Hauptverfasser: | , , , , , , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | n/a |
|---|---|
| container_issue | 9 |
| container_start_page | |
| container_title | European journal of organic chemistry |
| container_volume | 2022 |
| creator | Camilo, Nilton S. Santos, Hugo Zeoly, Lucas A. Fernandes, Fábio S. Rodrigues, Manoel T. Silva, Thiago S. Lima, Samia R. Serafim, José Cláudio Oliveira, Aline S. B. Carpanez, Arthur G. Amarante, Giovanni W. Coelho, Fernando |
| description | The Cover Feature illustrates the effect of acetic acid on the rate of the Morita–Baylis–Hillman reaction. The use of acetic acid as a fuel (additive) increases the reaction rate in all tested cases, with special emphasis on electron‐rich electrophilic partners. We believe that a general acid catalysis mechanism is responsible for this increase in reaction rate. More information can be found in the Research Article by G. W. Amarante, F. Coelho et al. |
| doi_str_mv | 10.1002/ejoc.202200183 |
| format | Article |
| fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_ejoc_202200183</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>EJOC202200183</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1293-8d18d809f6aebdc48d0fd9fbd3b7ed3b721eae99cecc8b49f97d3f2a486a01d13</originalsourceid><addsrcrecordid>eNqFkEFLw0AQhRdRsFavnueoh6S7SUiz3trQ2pZKxVrwFja7E5uSZMMmteTmT_DiH_SXmFDRo5eZxzDfg_cIuWbUZpQ6A9xpaTvUcShlgXtCeoxyblGf09NWe65nMe6-nJOLqtpRSrnvsx75DPUbGpiiqPcG72BUwDwvTXtU8Gh0raXOINEG6i3CgzZpLb7eP8aiydKqFbM0y3JRwBMKWae6gFGW6UMFm6I0KFFhUbdGY6OFgnVTtCZ1KmEtdYlwM9kbGxY2rMyrDeEWcxv4oAtwe0nOEpFVePWz-2QznTyHM2u5up-Ho6UlmcNdK1AsUAHliS8wVtILFE0UT2LlxkPshsNQIOcSpQxijyd8qNzEEV7gC8oUc_vEPvpKo6vKYBKVJs2FaSJGo67UqCs1-i21BfgROKQZNv98R5PFKvxjvwE8636A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Cover Feature: An Improved Protocol for the Morita‐Baylis‐Hillman Reaction Allows Unprecedented Broad Synthetic Scope (Eur. J. Org. Chem. 9/2022)</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Camilo, Nilton S. ; Santos, Hugo ; Zeoly, Lucas A. ; Fernandes, Fábio S. ; Rodrigues, Manoel T. ; Silva, Thiago S. ; Lima, Samia R. ; Serafim, José Cláudio ; Oliveira, Aline S. B. ; Carpanez, Arthur G. ; Amarante, Giovanni W. ; Coelho, Fernando</creator><creatorcontrib>Camilo, Nilton S. ; Santos, Hugo ; Zeoly, Lucas A. ; Fernandes, Fábio S. ; Rodrigues, Manoel T. ; Silva, Thiago S. ; Lima, Samia R. ; Serafim, José Cláudio ; Oliveira, Aline S. B. ; Carpanez, Arthur G. ; Amarante, Giovanni W. ; Coelho, Fernando</creatorcontrib><description>The Cover Feature illustrates the effect of acetic acid on the rate of the Morita–Baylis–Hillman reaction. The use of acetic acid as a fuel (additive) increases the reaction rate in all tested cases, with special emphasis on electron‐rich electrophilic partners. We believe that a general acid catalysis mechanism is responsible for this increase in reaction rate. More information can be found in the Research Article by G. W. Amarante, F. Coelho et al.</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.202200183</identifier><language>eng</language><subject>Brønsted acid ; C−C bond formation ; Morita-Baylis-Hillman ; Organocatalysis ; Sustainable chemistry</subject><ispartof>European journal of organic chemistry, 2022-03, Vol.2022 (9), p.n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-7411-5180 ; 0000-0002-3521-2172 ; 0000-0002-6231-8052 ; 0000-0001-8885-8762 ; 0000-0003-1407-6025 ; 0000-0001-9230-5642 ; 0000-0003-1004-5395 ; 0000-0003-1800-1549 ; 0000-0001-8476-8604 ; 0000-0003-1082-2289 ; 0000-0001-7041-8945 ; 0000-0003-2111-3904</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fejoc.202200183$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fejoc.202200183$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Camilo, Nilton S.</creatorcontrib><creatorcontrib>Santos, Hugo</creatorcontrib><creatorcontrib>Zeoly, Lucas A.</creatorcontrib><creatorcontrib>Fernandes, Fábio S.</creatorcontrib><creatorcontrib>Rodrigues, Manoel T.</creatorcontrib><creatorcontrib>Silva, Thiago S.</creatorcontrib><creatorcontrib>Lima, Samia R.</creatorcontrib><creatorcontrib>Serafim, José Cláudio</creatorcontrib><creatorcontrib>Oliveira, Aline S. B.</creatorcontrib><creatorcontrib>Carpanez, Arthur G.</creatorcontrib><creatorcontrib>Amarante, Giovanni W.</creatorcontrib><creatorcontrib>Coelho, Fernando</creatorcontrib><title>Cover Feature: An Improved Protocol for the Morita‐Baylis‐Hillman Reaction Allows Unprecedented Broad Synthetic Scope (Eur. J. Org. Chem. 9/2022)</title><title>European journal of organic chemistry</title><description>The Cover Feature illustrates the effect of acetic acid on the rate of the Morita–Baylis–Hillman reaction. The use of acetic acid as a fuel (additive) increases the reaction rate in all tested cases, with special emphasis on electron‐rich electrophilic partners. We believe that a general acid catalysis mechanism is responsible for this increase in reaction rate. More information can be found in the Research Article by G. W. Amarante, F. Coelho et al.</description><subject>Brønsted acid</subject><subject>C−C bond formation</subject><subject>Morita-Baylis-Hillman</subject><subject>Organocatalysis</subject><subject>Sustainable chemistry</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkEFLw0AQhRdRsFavnueoh6S7SUiz3trQ2pZKxVrwFja7E5uSZMMmteTmT_DiH_SXmFDRo5eZxzDfg_cIuWbUZpQ6A9xpaTvUcShlgXtCeoxyblGf09NWe65nMe6-nJOLqtpRSrnvsx75DPUbGpiiqPcG72BUwDwvTXtU8Gh0raXOINEG6i3CgzZpLb7eP8aiydKqFbM0y3JRwBMKWae6gFGW6UMFm6I0KFFhUbdGY6OFgnVTtCZ1KmEtdYlwM9kbGxY2rMyrDeEWcxv4oAtwe0nOEpFVePWz-2QznTyHM2u5up-Ho6UlmcNdK1AsUAHliS8wVtILFE0UT2LlxkPshsNQIOcSpQxijyd8qNzEEV7gC8oUc_vEPvpKo6vKYBKVJs2FaSJGo67UqCs1-i21BfgROKQZNv98R5PFKvxjvwE8636A</recordid><startdate>20220307</startdate><enddate>20220307</enddate><creator>Camilo, Nilton S.</creator><creator>Santos, Hugo</creator><creator>Zeoly, Lucas A.</creator><creator>Fernandes, Fábio S.</creator><creator>Rodrigues, Manoel T.</creator><creator>Silva, Thiago S.</creator><creator>Lima, Samia R.</creator><creator>Serafim, José Cláudio</creator><creator>Oliveira, Aline S. B.</creator><creator>Carpanez, Arthur G.</creator><creator>Amarante, Giovanni W.</creator><creator>Coelho, Fernando</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-7411-5180</orcidid><orcidid>https://orcid.org/0000-0002-3521-2172</orcidid><orcidid>https://orcid.org/0000-0002-6231-8052</orcidid><orcidid>https://orcid.org/0000-0001-8885-8762</orcidid><orcidid>https://orcid.org/0000-0003-1407-6025</orcidid><orcidid>https://orcid.org/0000-0001-9230-5642</orcidid><orcidid>https://orcid.org/0000-0003-1004-5395</orcidid><orcidid>https://orcid.org/0000-0003-1800-1549</orcidid><orcidid>https://orcid.org/0000-0001-8476-8604</orcidid><orcidid>https://orcid.org/0000-0003-1082-2289</orcidid><orcidid>https://orcid.org/0000-0001-7041-8945</orcidid><orcidid>https://orcid.org/0000-0003-2111-3904</orcidid></search><sort><creationdate>20220307</creationdate><title>Cover Feature: An Improved Protocol for the Morita‐Baylis‐Hillman Reaction Allows Unprecedented Broad Synthetic Scope (Eur. J. Org. Chem. 9/2022)</title><author>Camilo, Nilton S. ; Santos, Hugo ; Zeoly, Lucas A. ; Fernandes, Fábio S. ; Rodrigues, Manoel T. ; Silva, Thiago S. ; Lima, Samia R. ; Serafim, José Cláudio ; Oliveira, Aline S. B. ; Carpanez, Arthur G. ; Amarante, Giovanni W. ; Coelho, Fernando</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1293-8d18d809f6aebdc48d0fd9fbd3b7ed3b721eae99cecc8b49f97d3f2a486a01d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Brønsted acid</topic><topic>C−C bond formation</topic><topic>Morita-Baylis-Hillman</topic><topic>Organocatalysis</topic><topic>Sustainable chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Camilo, Nilton S.</creatorcontrib><creatorcontrib>Santos, Hugo</creatorcontrib><creatorcontrib>Zeoly, Lucas A.</creatorcontrib><creatorcontrib>Fernandes, Fábio S.</creatorcontrib><creatorcontrib>Rodrigues, Manoel T.</creatorcontrib><creatorcontrib>Silva, Thiago S.</creatorcontrib><creatorcontrib>Lima, Samia R.</creatorcontrib><creatorcontrib>Serafim, José Cláudio</creatorcontrib><creatorcontrib>Oliveira, Aline S. B.</creatorcontrib><creatorcontrib>Carpanez, Arthur G.</creatorcontrib><creatorcontrib>Amarante, Giovanni W.</creatorcontrib><creatorcontrib>Coelho, Fernando</creatorcontrib><collection>CrossRef</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Camilo, Nilton S.</au><au>Santos, Hugo</au><au>Zeoly, Lucas A.</au><au>Fernandes, Fábio S.</au><au>Rodrigues, Manoel T.</au><au>Silva, Thiago S.</au><au>Lima, Samia R.</au><au>Serafim, José Cláudio</au><au>Oliveira, Aline S. B.</au><au>Carpanez, Arthur G.</au><au>Amarante, Giovanni W.</au><au>Coelho, Fernando</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cover Feature: An Improved Protocol for the Morita‐Baylis‐Hillman Reaction Allows Unprecedented Broad Synthetic Scope (Eur. J. Org. Chem. 9/2022)</atitle><jtitle>European journal of organic chemistry</jtitle><date>2022-03-07</date><risdate>2022</risdate><volume>2022</volume><issue>9</issue><epage>n/a</epage><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>The Cover Feature illustrates the effect of acetic acid on the rate of the Morita–Baylis–Hillman reaction. The use of acetic acid as a fuel (additive) increases the reaction rate in all tested cases, with special emphasis on electron‐rich electrophilic partners. We believe that a general acid catalysis mechanism is responsible for this increase in reaction rate. More information can be found in the Research Article by G. W. Amarante, F. Coelho et al.</abstract><doi>10.1002/ejoc.202200183</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7411-5180</orcidid><orcidid>https://orcid.org/0000-0002-3521-2172</orcidid><orcidid>https://orcid.org/0000-0002-6231-8052</orcidid><orcidid>https://orcid.org/0000-0001-8885-8762</orcidid><orcidid>https://orcid.org/0000-0003-1407-6025</orcidid><orcidid>https://orcid.org/0000-0001-9230-5642</orcidid><orcidid>https://orcid.org/0000-0003-1004-5395</orcidid><orcidid>https://orcid.org/0000-0003-1800-1549</orcidid><orcidid>https://orcid.org/0000-0001-8476-8604</orcidid><orcidid>https://orcid.org/0000-0003-1082-2289</orcidid><orcidid>https://orcid.org/0000-0001-7041-8945</orcidid><orcidid>https://orcid.org/0000-0003-2111-3904</orcidid><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1434-193X |
| ispartof | European journal of organic chemistry, 2022-03, Vol.2022 (9), p.n/a |
| issn | 1434-193X 1099-0690 |
| language | eng |
| recordid | cdi_crossref_primary_10_1002_ejoc_202200183 |
| source | Wiley Online Library Journals Frontfile Complete |
| subjects | Brønsted acid C−C bond formation Morita-Baylis-Hillman Organocatalysis Sustainable chemistry |
| title | Cover Feature: An Improved Protocol for the Morita‐Baylis‐Hillman Reaction Allows Unprecedented Broad Synthetic Scope (Eur. J. Org. Chem. 9/2022) |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T23%3A39%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cover%20Feature:%20An%20Improved%20Protocol%20for%20the%20Morita%E2%80%90Baylis%E2%80%90Hillman%20Reaction%20Allows%20Unprecedented%20Broad%20Synthetic%20Scope%20(Eur.%20J.%20Org.%20Chem.%209/2022)&rft.jtitle=European%20journal%20of%20organic%20chemistry&rft.au=Camilo,%20Nilton%20S.&rft.date=2022-03-07&rft.volume=2022&rft.issue=9&rft.epage=n/a&rft.issn=1434-193X&rft.eissn=1099-0690&rft_id=info:doi/10.1002/ejoc.202200183&rft_dat=%3Cwiley_cross%3EEJOC202200183%3C/wiley_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 |