DSpace at KOASAS
College of Natural Sciences(자연과학대학)Dept. of Chemistry(화학과)CH-Journal Papers(저널논문)

Mother Diamine: A Universal Building Block for Making Chiral Ligands from Daughter Diamines to Binol, Binap and Monophos Analogues

Cited 3 time in webofscience Cited 3 time in scopus
  • Hit : 465
  • Download : 0
Export
DC FieldValueLanguage
dc.contributor.authorLee, An Sooko
dc.contributor.authorSo, Soon Mogko
dc.contributor.authorLough, Alan J.ko
dc.contributor.authorKim, Hyunwooko
dc.contributor.authorChin, Jikko
dc.date.accessioned2015-01-27T01:41:05Z-
dc.date.available2015-01-27T01:41:05Z-
dc.date.created2014-11-11-
dc.date.created2014-11-11-
dc.date.created2014-11-11-
dc.date.issued2014-10-
dc.identifier.citationASIAN JOURNAL OF ORGANIC CHEMISTRY, v.3, no.10, pp.1102 - 1107-
dc.identifier.issn2193-5807-
dc.identifier.urihttp://hdl.handle.net/10203/193006-
dc.description.abstract"Mother diamine" (MD) or 1,2-bis(2-hydroxy-phenyl) ethylenediamine can be rapidly transformed to a wide variety of chiral ligands including vicinal diamines and analogs of binol (MDdiol), binap (MDdiphos), and monophos (MDphos). The reactivity and stereoselectivity of the MDphos ligands in Rh-catalyzed hydrogenation are highly sensitive to the N, N'-dialkyl substituents.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleMother Diamine: A Universal Building Block for Making Chiral Ligands from Daughter Diamines to Binol, Binap and Monophos Analogues-
dc.typeArticle-
dc.identifier.wosid000342895700012-
dc.identifier.scopusid2-s2.0-85027923205-
dc.type.rimsART-
dc.citation.volume3-
dc.citation.issue10-
dc.citation.beginningpage1102-
dc.citation.endingpage1107-
dc.citation.publicationnameASIAN JOURNAL OF ORGANIC CHEMISTRY-
dc.identifier.doi10.1002/ajoc.201402135-
dc.contributor.localauthorKim, Hyunwoo-
dc.contributor.nonIdAuthorSo, Soon Mog-
dc.contributor.nonIdAuthorLough, Alan J.-
dc.contributor.nonIdAuthorChin, Jik-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorasymmetric hydrogenation-
dc.subject.keywordAuthordiamines-
dc.subject.keywordAuthorphosphane ligands-
dc.subject.keywordAuthorreductive amination-
dc.subject.keywordAuthorsynthetic methods-
dc.subject.keywordPlusDIAZA-COPE REARRANGEMENT-
dc.subject.keywordPlusCATALYZED ENANTIOSELECTIVE HYDROGENATION-
dc.subject.keywordPlusMONODENTATE PHOSPHORAMIDITE LIGANDS-
dc.subject.keywordPlusDYNAMIC KINETIC RESOLUTION-
dc.subject.keywordPlusSUZUKI CROSS-COUPLINGS-
dc.subject.keywordPlusALPHA-KETO ESTERS-
dc.subject.keywordPlusASYMMETRIC HYDROGENATION-
dc.subject.keywordPlusSTEREOSPECIFIC SYNTHESIS-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusACIDS-
Appears in Collection
CH-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 3 items in WoS Click to see citing articles in records_button

Display Simple Item Record

qr_code

  • mendeley

    citeulike

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.


rss_1.0 rss_2.0 atom_1.0