Zinc Di(l-prolinate)-Mediated Synthesis of α-Aminophosphonates under Mild Conditions
Abstract An efficient method has been developed for the preparation of α-aminophosphonates by using zinc di( l -prolinate) as a catalyst under mild reaction conditions. The method has the advantages of high yields, short reaction times, and easy workup conditions.
Gespeichert in:
| Veröffentlicht in: | Synthesis (Stuttgart) 2016-12, Vol.48 (24), p.4489-4494 |
|---|---|
| Hauptverfasser: | , , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 4494 |
|---|---|
| container_issue | 24 |
| container_start_page | 4489 |
| container_title | Synthesis (Stuttgart) |
| container_volume | 48 |
| creator | de Oliveira, Aline R. Katla, Ramesh Rocha, Mariana P. D. Albuquerque, Tábata B. da Silva, Caren D. G. Kupfer, Vicente L. Rinaldi, Andrelson W. Domingues, Nelson Luís Campos |
| description | Abstract
An efficient method has been developed for the preparation of α-aminophosphonates by using zinc di(
l
-prolinate) as a catalyst under mild reaction conditions. The method has the advantages of high yields, short reaction times, and easy workup conditions. |
| doi_str_mv | 10.1055/s-0036-1588065 |
| format | Article |
| fullrecord | <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_0036_1588065</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_0036_1588065</sourcerecordid><originalsourceid>FETCH-LOGICAL-c277t-dd362a22fb08ac3466e2e7caf01780eec51c7ab1b09192d4b1a5e763f068212d3</originalsourceid><addsrcrecordid>eNp1kM1KAzEUhYMoWKtb11nqIvUm6SQzy1J_ocWFFsRNyCQZmjJNSjJd9LF8EZ_JGdqti8u9cM85HD6EbilMKBTFQyYAXBBalCWI4gyN6JRLwih8naNR_6qILEt6ia5y3gCAZLwaodW3DwY_-ruW7FJsfdCduydLZ31_WPxxCN3aZZ9xbPDvD5ltfYi7dcz9DNKM98G6hJe-tXgeg_WdjyFfo4tGt9ndnPYYrZ6fPuevZPH-8jafLYhhUnbEWi6YZqypodSGT4VwzEmjG6CyBOdMQY3UNa2hohWz05rqwknBGxAlo8zyMZocc02KOSfXqF3yW50OioIaoKisBijqBKU3kKOhW3u3dWoT9yn0Df_T_wHLvGQe</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Zinc Di(l-prolinate)-Mediated Synthesis of α-Aminophosphonates under Mild Conditions</title><source>Thieme Connect Journals</source><creator>de Oliveira, Aline R. ; Katla, Ramesh ; Rocha, Mariana P. D. ; Albuquerque, Tábata B. ; da Silva, Caren D. G. ; Kupfer, Vicente L. ; Rinaldi, Andrelson W. ; Domingues, Nelson Luís Campos</creator><creatorcontrib>de Oliveira, Aline R. ; Katla, Ramesh ; Rocha, Mariana P. D. ; Albuquerque, Tábata B. ; da Silva, Caren D. G. ; Kupfer, Vicente L. ; Rinaldi, Andrelson W. ; Domingues, Nelson Luís Campos</creatorcontrib><description>Abstract
An efficient method has been developed for the preparation of α-aminophosphonates by using zinc di(
l
-prolinate) as a catalyst under mild reaction conditions. The method has the advantages of high yields, short reaction times, and easy workup conditions.</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/s-0036-1588065</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag</publisher><ispartof>Synthesis (Stuttgart), 2016-12, Vol.48 (24), p.4489-4494</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c277t-dd362a22fb08ac3466e2e7caf01780eec51c7ab1b09192d4b1a5e763f068212d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1588065.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0036-1588065$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,780,784,3017,3018,27924,27925,54559,54560</link.rule.ids></links><search><creatorcontrib>de Oliveira, Aline R.</creatorcontrib><creatorcontrib>Katla, Ramesh</creatorcontrib><creatorcontrib>Rocha, Mariana P. D.</creatorcontrib><creatorcontrib>Albuquerque, Tábata B.</creatorcontrib><creatorcontrib>da Silva, Caren D. G.</creatorcontrib><creatorcontrib>Kupfer, Vicente L.</creatorcontrib><creatorcontrib>Rinaldi, Andrelson W.</creatorcontrib><creatorcontrib>Domingues, Nelson Luís Campos</creatorcontrib><title>Zinc Di(l-prolinate)-Mediated Synthesis of α-Aminophosphonates under Mild Conditions</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>Abstract
An efficient method has been developed for the preparation of α-aminophosphonates by using zinc di(
l
-prolinate) as a catalyst under mild reaction conditions. The method has the advantages of high yields, short reaction times, and easy workup conditions.</description><issn>0039-7881</issn><issn>1437-210X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1kM1KAzEUhYMoWKtb11nqIvUm6SQzy1J_ocWFFsRNyCQZmjJNSjJd9LF8EZ_JGdqti8u9cM85HD6EbilMKBTFQyYAXBBalCWI4gyN6JRLwih8naNR_6qILEt6ia5y3gCAZLwaodW3DwY_-ruW7FJsfdCduydLZ31_WPxxCN3aZZ9xbPDvD5ltfYi7dcz9DNKM98G6hJe-tXgeg_WdjyFfo4tGt9ndnPYYrZ6fPuevZPH-8jafLYhhUnbEWi6YZqypodSGT4VwzEmjG6CyBOdMQY3UNa2hohWz05rqwknBGxAlo8zyMZocc02KOSfXqF3yW50OioIaoKisBijqBKU3kKOhW3u3dWoT9yn0Df_T_wHLvGQe</recordid><startdate>20161215</startdate><enddate>20161215</enddate><creator>de Oliveira, Aline R.</creator><creator>Katla, Ramesh</creator><creator>Rocha, Mariana P. D.</creator><creator>Albuquerque, Tábata B.</creator><creator>da Silva, Caren D. G.</creator><creator>Kupfer, Vicente L.</creator><creator>Rinaldi, Andrelson W.</creator><creator>Domingues, Nelson Luís Campos</creator><general>Georg Thieme Verlag</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20161215</creationdate><title>Zinc Di(l-prolinate)-Mediated Synthesis of α-Aminophosphonates under Mild Conditions</title><author>de Oliveira, Aline R. ; Katla, Ramesh ; Rocha, Mariana P. D. ; Albuquerque, Tábata B. ; da Silva, Caren D. G. ; Kupfer, Vicente L. ; Rinaldi, Andrelson W. ; Domingues, Nelson Luís Campos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c277t-dd362a22fb08ac3466e2e7caf01780eec51c7ab1b09192d4b1a5e763f068212d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Oliveira, Aline R.</creatorcontrib><creatorcontrib>Katla, Ramesh</creatorcontrib><creatorcontrib>Rocha, Mariana P. D.</creatorcontrib><creatorcontrib>Albuquerque, Tábata B.</creatorcontrib><creatorcontrib>da Silva, Caren D. G.</creatorcontrib><creatorcontrib>Kupfer, Vicente L.</creatorcontrib><creatorcontrib>Rinaldi, Andrelson W.</creatorcontrib><creatorcontrib>Domingues, Nelson Luís Campos</creatorcontrib><collection>CrossRef</collection><jtitle>Synthesis (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Oliveira, Aline R.</au><au>Katla, Ramesh</au><au>Rocha, Mariana P. D.</au><au>Albuquerque, Tábata B.</au><au>da Silva, Caren D. G.</au><au>Kupfer, Vicente L.</au><au>Rinaldi, Andrelson W.</au><au>Domingues, Nelson Luís Campos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Zinc Di(l-prolinate)-Mediated Synthesis of α-Aminophosphonates under Mild Conditions</atitle><jtitle>Synthesis (Stuttgart)</jtitle><addtitle>Synthesis</addtitle><date>2016-12-15</date><risdate>2016</risdate><volume>48</volume><issue>24</issue><spage>4489</spage><epage>4494</epage><pages>4489-4494</pages><issn>0039-7881</issn><eissn>1437-210X</eissn><abstract>Abstract
An efficient method has been developed for the preparation of α-aminophosphonates by using zinc di(
l
-prolinate) as a catalyst under mild reaction conditions. The method has the advantages of high yields, short reaction times, and easy workup conditions.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0036-1588065</doi><tpages>6</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0039-7881 |
| ispartof | Synthesis (Stuttgart), 2016-12, Vol.48 (24), p.4489-4494 |
| issn | 0039-7881 1437-210X |
| language | eng |
| recordid | cdi_crossref_primary_10_1055_s_0036_1588065 |
| source | Thieme Connect Journals |
| title | Zinc Di(l-prolinate)-Mediated Synthesis of α-Aminophosphonates under Mild Conditions |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T03%3A47%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Zinc%20Di(l-prolinate)-Mediated%20Synthesis%20of%20%CE%B1-Aminophosphonates%20under%20Mild%20Conditions&rft.jtitle=Synthesis%20(Stuttgart)&rft.au=de%20Oliveira,%20Aline%20R.&rft.date=2016-12-15&rft.volume=48&rft.issue=24&rft.spage=4489&rft.epage=4494&rft.pages=4489-4494&rft.issn=0039-7881&rft.eissn=1437-210X&rft_id=info:doi/10.1055/s-0036-1588065&rft_dat=%3Cthieme_cross%3E10_1055_s_0036_1588065%3C/thieme_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 |