File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Synthesis and application of diphenyl sulfide linked bis(imidazoline) ligands: Dramatic electronic effect of ligands on catalytic behavior

TitleSynthesis and application of diphenyl sulfide linked bis(imidazoline) ligands: Dramatic electronic effect of ligands on catalytic behavior
Authors
KeywordsAlkylation
Asymmetric catalysis
Imidazoline
Substituent effects
Sulfur
Issue Date2011
Citation
European Journal of Organic Chemistry, 2011, v. 2011 n. 4, p. 786-793 How to Cite?
AbstractDiphenyl sulfide linked bis(imidazoline) ligands with electron-withdrawing N-Ts substitution and electron-donating N-alkyl or N-H substitutions were synthesized through different routes. The electronic effects of the ligands were tuned rationally, and dramatic variation in their catalytic behavior was observed. N-Alkyl and N-H ligands demonstrated much higher catalytic activity and improved enantioselectivity than N-Ts ligands in Pd-catalyzed asymmetric allylic alkylation reactions. Diphenyl sulfide linked bis(imidazoline) ligands were synthesized. The electronic effects of the ligands were tuned rationally, and dramatic variation in their catalytic behavior was observed. N-Alkyl and N-H ligands showed much higher catalytic activity and improved enantioselectivity over N-Ts ligands in Pd-catalyzed asymmetric allylic alkylation reactions. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Persistent Identifierhttp://hdl.handle.net/10722/292017
ISSN
2021 Impact Factor: 3.261
2020 SCImago Journal Rankings: 0.825
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorDu, Xian-
dc.contributor.authorLiu, Han-
dc.contributor.authorDu, Da Ming-
dc.date.accessioned2020-11-17T14:55:36Z-
dc.date.available2020-11-17T14:55:36Z-
dc.date.issued2011-
dc.identifier.citationEuropean Journal of Organic Chemistry, 2011, v. 2011 n. 4, p. 786-793-
dc.identifier.issn1434-193X-
dc.identifier.urihttp://hdl.handle.net/10722/292017-
dc.description.abstractDiphenyl sulfide linked bis(imidazoline) ligands with electron-withdrawing N-Ts substitution and electron-donating N-alkyl or N-H substitutions were synthesized through different routes. The electronic effects of the ligands were tuned rationally, and dramatic variation in their catalytic behavior was observed. N-Alkyl and N-H ligands demonstrated much higher catalytic activity and improved enantioselectivity than N-Ts ligands in Pd-catalyzed asymmetric allylic alkylation reactions. Diphenyl sulfide linked bis(imidazoline) ligands were synthesized. The electronic effects of the ligands were tuned rationally, and dramatic variation in their catalytic behavior was observed. N-Alkyl and N-H ligands showed much higher catalytic activity and improved enantioselectivity over N-Ts ligands in Pd-catalyzed asymmetric allylic alkylation reactions. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.-
dc.languageeng-
dc.relation.ispartofEuropean Journal of Organic Chemistry-
dc.subjectAlkylation-
dc.subjectAsymmetric catalysis-
dc.subjectImidazoline-
dc.subjectSubstituent effects-
dc.subjectSulfur-
dc.titleSynthesis and application of diphenyl sulfide linked bis(imidazoline) ligands: Dramatic electronic effect of ligands on catalytic behavior-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/ejoc.201001347-
dc.identifier.scopuseid_2-s2.0-79251614395-
dc.identifier.volume2011-
dc.identifier.issue4-
dc.identifier.spage786-
dc.identifier.epage793-
dc.identifier.eissn1099-0690-
dc.identifier.isiWOS:000287163000016-
dc.identifier.issnl1099-0690-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats