Literatura académica sobre el tema "Suzuki-Miyaura domino coupling"
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Artículos de revistas sobre el tema "Suzuki-Miyaura domino coupling"
Akkarasamiyo, Sunisa, Somsak Ruchirawat, Poonsaksi Ploypradith y Joseph S. M. Samec. "Transition-Metal-Catalyzed Suzuki–Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols". Synthesis 52, n.º 05 (7 de enero de 2020): 645–59. http://dx.doi.org/10.1055/s-0039-1690740.
Texto completoKazemnejadi, Milad, Rebin Omer Ahmed y 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, n.º 72 (2020): 43962–74. http://dx.doi.org/10.1039/d0ra08344e.
Texto completoAsgari, M., R. Mirzazadeh, B. Larijani, P. Rashidi Ranjbar, R. Rahimi y M. Mahdavi. "Palladium-Catalyzed Regioselective Heck–Suzuki–Miyaura Cascade Cyclization for the Synthesis of Trisubstituted Arylideneisoquinolinones". Synlett 30, n.º 09 (18 de abril de 2019): 1073–76. http://dx.doi.org/10.1055/s-0037-1611804.
Texto completoGruß, Hendrik, Rebecca C. Feiner, Ridhiwan Mseya, David C. Schröder, Michał Jewgiński, Kristian M. Müller, Rafał Latajka, Antoine Marion y Norbert Sewald. "Peptide stapling by late-stage Suzuki–Miyaura cross-coupling". Beilstein Journal of Organic Chemistry 18 (3 de enero de 2022): 1–12. http://dx.doi.org/10.3762/bjoc.18.1.
Texto completoTesis sobre el tema "Suzuki-Miyaura domino coupling"
Bochicchio, Antonella. "Towards the atropo-stereoselective total synthesis of myricanol". Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF004/document.
Texto completoThe 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.
Texto completoThe 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.
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