Dergi makalesi Açık Erişim
Havare, Nizam
<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd"> <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/6451</identifier> <creators> <creator> <creatorName>Havare, Nizam</creatorName> <givenName>Nizam</givenName> <familyName>Havare</familyName> <affiliation>Stanford Univ, Sch Humanities & Sci, Dept Chem, Stanford, CA 94305 USA</affiliation> </creator> </creators> <titles> <title>Effective Synthesis Of Bicyclodienes Via Palladium-Catalyzed Asymmetric Allylic Alkylation And Ruthenium-Catalyzed Cycloisomerization</title> </titles> <publisher>Aperta</publisher> <publicationYear>2020</publicationYear> <dates> <date dateType="Issued">2020-01-01</date> </dates> <resourceType resourceTypeGeneral="Text">Journal article</resourceType> <alternateIdentifiers> <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/6451</alternateIdentifier> </alternateIdentifiers> <relatedIdentifiers> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.3906/kim-2004-81</relatedIdentifier> </relatedIdentifiers> <rightsList> <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights> <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights> </rightsList> <descriptions> <description descriptionType="Abstract">[n.3.0]Bicycles (n = 3-6) can be synthesized using palladium-catalyzed asymmetric allylic alkylation followed by ruthenium-catalyzed cycloisomerization. New types oftriarylphosphino-1,2- diaminooxazoline ligands show the same high levels of enantioselectivity observed with Trost ligand when employed in Pd-catalyzed allylic alkylation reactions. The enyne products of these allylic alkylation reactions were further elaborated using a Ru-catalyzed redox isomerization process, for which a mechanism is proposed.</description> </descriptions> </resource>
Görüntülenme | 57 |
İndirme | 16 |
Veri hacmi | 585.1 MB |
Tekil görüntülenme | 52 |
Tekil indirme | 16 |