Tunable coordination of a tropos phosphite for fine-tuning of the Rh catalyzed asymmetric addition of phenylboronic acid to cyclohexenone
Using the deoxycholic acid derived tropos biphenylphosphite as a Rh(i) chiral ligand different complexes are obtained, depending on the Rh : L molar ratio, that give rise to the formation of different chiral products in the asymmetric addition of phenylboronic acid to cyclohexenone.
Gespeichert in:
Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2009-01 (4), p.457-459 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 459 |
---|---|
container_issue | 4 |
container_start_page | 457 |
container_title | Chemical communications (Cambridge, England) |
container_volume | |
creator | Iuliano, Anna Facchetti, Sarah Funaioli, Tiziana |
description | Using the deoxycholic acid derived tropos biphenylphosphite as a Rh(i) chiral ligand different complexes are obtained, depending on the Rh : L molar ratio, that give rise to the formation of different chiral products in the asymmetric addition of phenylboronic acid to cyclohexenone. |
doi_str_mv | 10.1039/b814568g |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_66813759</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>66813759</sourcerecordid><originalsourceid>FETCH-LOGICAL-p209t-8d3e12c92830606556c1f98d2fcd100ae330624669ddf46d1f1f50df107823f33</originalsourceid><addsrcrecordid>eNo1kM1KxDAcxHNQ3HUVfALJyVs1adpscpTFL1gQZD2XNPlnG2mT2qRgfQPf2oq7cxmY-TGHQeiKkltKmLyrBS1KLvYnaElZKbM1K8oFOo_xg8yipThDCyopW1NRLNHPbvSqbgHrEAbjvEoueBwsVjgNoQ8R902IfeMSYBsGbJ2HLI3e-f0flRrAbw3WKql2-gaDVZy6DtLgNFbGuONa34Cf2joMwf812hmcAtaTbkMDX-CDhwt0alUb4fLgK_T--LDbPGfb16eXzf0263MiUyYMA5prmQtGOOFlyTW1UpjcakMJUcDmPC84l8bYghtqqS2JsZSsRc4sYyt087_bD-FzhJiqzkUNbas8hDFWnIv5nFLO4PUBHOsOTNUPrlPDVB3PY7-6IXBy</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>66813759</pqid></control><display><type>article</type><title>Tunable coordination of a tropos phosphite for fine-tuning of the Rh catalyzed asymmetric addition of phenylboronic acid to cyclohexenone</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Iuliano, Anna ; Facchetti, Sarah ; Funaioli, Tiziana</creator><creatorcontrib>Iuliano, Anna ; Facchetti, Sarah ; Funaioli, Tiziana</creatorcontrib><description>Using the deoxycholic acid derived tropos biphenylphosphite as a Rh(i) chiral ligand different complexes are obtained, depending on the Rh : L molar ratio, that give rise to the formation of different chiral products in the asymmetric addition of phenylboronic acid to cyclohexenone.</description><identifier>ISSN: 1359-7345</identifier><identifier>DOI: 10.1039/b814568g</identifier><identifier>PMID: 19137184</identifier><language>eng</language><publisher>England</publisher><ispartof>Chemical communications (Cambridge, England), 2009-01 (4), p.457-459</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19137184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iuliano, Anna</creatorcontrib><creatorcontrib>Facchetti, Sarah</creatorcontrib><creatorcontrib>Funaioli, Tiziana</creatorcontrib><title>Tunable coordination of a tropos phosphite for fine-tuning of the Rh catalyzed asymmetric addition of phenylboronic acid to cyclohexenone</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>Using the deoxycholic acid derived tropos biphenylphosphite as a Rh(i) chiral ligand different complexes are obtained, depending on the Rh : L molar ratio, that give rise to the formation of different chiral products in the asymmetric addition of phenylboronic acid to cyclohexenone.</description><issn>1359-7345</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNo1kM1KxDAcxHNQ3HUVfALJyVs1adpscpTFL1gQZD2XNPlnG2mT2qRgfQPf2oq7cxmY-TGHQeiKkltKmLyrBS1KLvYnaElZKbM1K8oFOo_xg8yipThDCyopW1NRLNHPbvSqbgHrEAbjvEoueBwsVjgNoQ8R902IfeMSYBsGbJ2HLI3e-f0flRrAbw3WKql2-gaDVZy6DtLgNFbGuONa34Cf2joMwf812hmcAtaTbkMDX-CDhwt0alUb4fLgK_T--LDbPGfb16eXzf0263MiUyYMA5prmQtGOOFlyTW1UpjcakMJUcDmPC84l8bYghtqqS2JsZSsRc4sYyt087_bD-FzhJiqzkUNbas8hDFWnIv5nFLO4PUBHOsOTNUPrlPDVB3PY7-6IXBy</recordid><startdate>20090128</startdate><enddate>20090128</enddate><creator>Iuliano, Anna</creator><creator>Facchetti, Sarah</creator><creator>Funaioli, Tiziana</creator><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20090128</creationdate><title>Tunable coordination of a tropos phosphite for fine-tuning of the Rh catalyzed asymmetric addition of phenylboronic acid to cyclohexenone</title><author>Iuliano, Anna ; Facchetti, Sarah ; Funaioli, Tiziana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p209t-8d3e12c92830606556c1f98d2fcd100ae330624669ddf46d1f1f50df107823f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iuliano, Anna</creatorcontrib><creatorcontrib>Facchetti, Sarah</creatorcontrib><creatorcontrib>Funaioli, Tiziana</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iuliano, Anna</au><au>Facchetti, Sarah</au><au>Funaioli, Tiziana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tunable coordination of a tropos phosphite for fine-tuning of the Rh catalyzed asymmetric addition of phenylboronic acid to cyclohexenone</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2009-01-28</date><risdate>2009</risdate><issue>4</issue><spage>457</spage><epage>459</epage><pages>457-459</pages><issn>1359-7345</issn><abstract>Using the deoxycholic acid derived tropos biphenylphosphite as a Rh(i) chiral ligand different complexes are obtained, depending on the Rh : L molar ratio, that give rise to the formation of different chiral products in the asymmetric addition of phenylboronic acid to cyclohexenone.</abstract><cop>England</cop><pmid>19137184</pmid><doi>10.1039/b814568g</doi><tpages>3</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1359-7345 |
ispartof | Chemical communications (Cambridge, England), 2009-01 (4), p.457-459 |
issn | 1359-7345 |
language | eng |
recordid | cdi_proquest_miscellaneous_66813759 |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Tunable coordination of a tropos phosphite for fine-tuning of the Rh catalyzed asymmetric addition of phenylboronic acid to cyclohexenone |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T05%3A21%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tunable%20coordination%20of%20a%20tropos%20phosphite%20for%20fine-tuning%20of%20the%20Rh%20catalyzed%20asymmetric%20addition%20of%20phenylboronic%20acid%20to%20cyclohexenone&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Iuliano,%20Anna&rft.date=2009-01-28&rft.issue=4&rft.spage=457&rft.epage=459&rft.pages=457-459&rft.issn=1359-7345&rft_id=info:doi/10.1039/b814568g&rft_dat=%3Cproquest_pubme%3E66813759%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=66813759&rft_id=info:pmid/19137184&rfr_iscdi=true |