Auswahl der wissenschaftlichen Literatur zum Thema „Suzuki-Miyaura domino coupling“
Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an
Inhaltsverzeichnis
Machen Sie sich mit den Listen der aktuellen Artikel, Bücher, Dissertationen, Berichten und anderer wissenschaftlichen Quellen zum Thema "Suzuki-Miyaura domino coupling" bekannt.
Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.
Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.
Zeitschriftenartikel zum Thema "Suzuki-Miyaura domino coupling"
Akkarasamiyo, Sunisa, Somsak Ruchirawat, Poonsaksi Ploypradith und Joseph S. M. Samec. „Transition-Metal-Catalyzed Suzuki–Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols“. Synthesis 52, Nr. 05 (07.01.2020): 645–59. http://dx.doi.org/10.1055/s-0039-1690740.
Der volle Inhalt der QuelleKazemnejadi, Milad, Rebin Omer Ahmed und Boshra Mahmoudi. „Ni/Pd-catalyzed Suzuki–Miyaura cross-coupling of alcohols and aldehydes and C–N cross-coupling of nitro and amines via domino redox reactions: base-free, hydride acceptor-free“. RSC Advances 10, Nr. 72 (2020): 43962–74. http://dx.doi.org/10.1039/d0ra08344e.
Der volle Inhalt der QuelleAsgari, M., R. Mirzazadeh, B. Larijani, P. Rashidi Ranjbar, R. Rahimi und M. Mahdavi. „Palladium-Catalyzed Regioselective Heck–Suzuki–Miyaura Cascade Cyclization for the Synthesis of Trisubstituted Arylideneisoquinolinones“. Synlett 30, Nr. 09 (18.04.2019): 1073–76. http://dx.doi.org/10.1055/s-0037-1611804.
Der volle Inhalt der QuelleGruß, Hendrik, Rebecca C. Feiner, Ridhiwan Mseya, David C. Schröder, Michał Jewgiński, Kristian M. Müller, Rafał Latajka, Antoine Marion und Norbert Sewald. „Peptide stapling by late-stage Suzuki–Miyaura cross-coupling“. Beilstein Journal of Organic Chemistry 18 (03.01.2022): 1–12. http://dx.doi.org/10.3762/bjoc.18.1.
Der volle Inhalt der QuelleDissertationen zum Thema "Suzuki-Miyaura domino coupling"
Bochicchio, Antonella. „Towards the atropo-stereoselective total synthesis of myricanol“. Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF004/document.
Der volle Inhalt der QuelleThe myricanol, a natural [7.0]-meta-cyclophane which belongs to the family of strained and cyclic diarylheptanoids, possess an interesting structure and attractive biologically activities (anti Alzheimer and anti cancer properties). Actually only two synthesis of racemic (+/-)-myricanol have been reported in the literature. The goal of this research was to prepare this strained cyclophane in a racemic and then in an atropostereoselective route taking into account the challenging ring closure. Thus a linear diarylheptanoid was prepared using an efficient cross-metathesis reaction followed by an intramolecular Suzuki-Miyaura domino reaction giving rise to the desired cyclophane with 2.55% overall yield in 11 steps. On the other side, the biaryl core of myricanol was envisaged by an intermolecular metallo-catalysed coupling reaction between already highly functionalized fragments, followed by a ring closure metathesis. Two advanced intermediates were already attempted
Santarsiere, Alessandro. „A new total synthesis of myricanol : the influence of an ene-yne system“. Electronic Thesis or Diss., Strasbourg, 2024. https://publication-theses.unistra.fr/public/theses_doctorat/2024/Santarsiere_Alessandro_2024_ED222.pdf.
Der volle Inhalt der QuelleThe main objective of this thesis is the total synthesis of myricanol, a natural compound with significant biological activities. In particular, its remarkable anti-Alzheimer's properties make it a potential drug for the treatment of various tauopathies, as it has the ability to reduce levels of tau protein that tend to pathologically accumulate in phosphorylated forms in certain neurodegenerative diseases. Actually only three synthesis of racemic (+/-) - myricanol have been reported in the literature. Firstly, this thesis aims primarily to investigate the optimal conditions to make cyclization less unfavorable using an unsaturated and thus "rigid" seco-precursor to limit conformational degrees of freedom during cyclization. Two main synthetic approacheshave been explored in the course of this thesis, on one side, the macrocyclization involves the properly functionalized biaryl system, on the other side the macrocyclization is performed on a linear diarylheptanoid
Heidemann, Sven. „Untersuchungen zur enantioselektiven Totalsynthese von Parnafungin C“. Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2016. http://hdl.handle.net/11858/00-1735-0000-002B-7C16-4.
Der volle Inhalt der Quelle