Relevant bibliographies by topics / Liebeskind-Srogl

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Liebeskind-Srogl'

Author: Grafiati
Published: 4 June 2021
Last updated: 5 February 2022

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Journal articles on the topic "Liebeskind-Srogl"

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Schaaf, Patricia, Thomas Bayer, Moumita Koley, et al. "Biocompatible metal-assisted C–C cross-coupling combined with biocatalytic chiral reductions in a concurrent tandem cascade." Chemical Communications 54, no. 92 (2018): 12978–81. http://dx.doi.org/10.1039/c8cc05304a.

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We present a concurrent chemo/biocatalytic one pot reaction cascade by combining a metal (Pd/Cu) assisted Liebeskind–Srogl coupling with an enantioselective enzymatic reduction for the production of chiral amines and alcohols.
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Yang, Quanlu, Zhengjun Quan, Baoxin Du, et al. "Wool-anchored Pd(OAc)2 complex: a highly active and reusable catalyst for desulfurative coupling reactions." Catalysis Science & Technology 5, no. 9 (2015): 4522–31. http://dx.doi.org/10.1039/c5cy00802f.

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A biomacromolecule-anchored palladium complex, wool-Pd(OAc)<sub>2</sub>, was used as a catalyst for the Liebeskind–Srogl desulfurative coupling reactions of pyrimidin-yl thioether derivatives with terminal alkynes and arylboronic acids.
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Dandepally, Srinivasa Reddy, and Alfred L. Williams. "Liebeskind–Srogl cross coupling mediated synthesis of verbenachalcone." Tetrahedron Letters 51, no. 44 (2010): 5753–56. http://dx.doi.org/10.1016/j.tetlet.2010.08.073.

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Prokopcová, Hana, and C. Oliver Kappe. "Die C-C-Kreuzkupplung nach Liebeskind und Srogl." Angewandte Chemie 121, no. 13 (2009): 2312–22. http://dx.doi.org/10.1002/ange.200802842.

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Prokopcová, Hana, and C. Oliver Kappe. "The Liebeskind-Srogl CC Cross-Coupling Reaction." Angewandte Chemie International Edition 48, no. 13 (2008): 2276–86. http://dx.doi.org/10.1002/anie.200802842.

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Ma, Yuanhong, Jose Cammarata, and Josep Cornella. "Ni-Catalyzed Reductive Liebeskind–Srogl Alkylation of Heterocycles." Journal of the American Chemical Society 141, no. 5 (2019): 1918–22. http://dx.doi.org/10.1021/jacs.8b13534.

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Piqani, Bruno, and Wei Zhang. "Synthesis of diverse dihydropyrimidine-related scaffolds by fluorous benzaldehyde-based Biginelli reaction and post-condensation modifications." Beilstein Journal of Organic Chemistry 7 (September 16, 2011): 1294–98. http://dx.doi.org/10.3762/bjoc.7.150.

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Dihydropyrimidinones and dihydropyrimidinethiones generated from the Biginelli reactions of perfluorooctanesulfonyl-attached benzaldehydes are used as common intermediates for post-condensation modifications such as cycloaddition, Liebeskind–Srogl reaction and Suzuki coupling to form biaryl-substituted dihydropyrimidinone, dihydropyrimidine, and thiazolopyrimidine compounds. The high efficiency of the diversity-oriented synthesis is achieved by conducting a multicomponent reaction for improved atom economy, under microwave heating for fast reaction, and with fluorous solid-phase extractions (F
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Sun, Qi, Franck Suzenet, and Gérald Guillaumet. "Optimized Liebeskind–Srogl coupling reaction between dihydropyrimidines and tributyltin compounds." Tetrahedron Letters 53, no. 22 (2012): 2694–98. http://dx.doi.org/10.1016/j.tetlet.2012.03.067.

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Fujii, Tomohiro, Yuta Oki, and Masahisa Nakada. "Research on Liebeskind-Srogl coupling/intramolecular Diels-Alder reaction cascade." Tetrahedron Letters 59, no. 10 (2018): 882–86. http://dx.doi.org/10.1016/j.tetlet.2018.01.046.

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Han, Junyan, Oswaldo Gonzalez, Angelica Aguilar-Aguilar, Eduardo Peña-Cabrera, and Kevin Burgess. "3- and 5-Functionalized BODIPYs via the Liebeskind-Srogl reaction." Org. Biomol. Chem. 7, no. 1 (2009): 34–36. http://dx.doi.org/10.1039/b818390b.

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Dissertations / Theses on the topic "Liebeskind-Srogl"

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Dahbi, Samir. "Chimie innovante en série dioxyde de quinoxaline : vers de nouveaux antituberculeux, inhibiteurs de la biosynthèse des mycobactines." Thesis, Mulhouse, 2012. http://www.theses.fr/2012MULH4078.

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Afin d'internaliser le fer, un micronutriment essentiel pour sa survie, Mycobacterium tuberculosis, la mycobactérie responsable de la tuberculose, biosynthétise des composés ayant une très grande affinité pour Fe3+ appelés les mycobactines. Ces sidérophores sont biosynthétisés par voie non­ ribosomale, la synthèse débutant par l'activation d'une molécule d'acide salicylique par l'enzyme d'adénylation mbtA sous la forme d'un dérivé ester d'adénosylmonophosphate (salicyl-AMP). Notre laboratoire a déjà préparé des analogues stables de salicyl-AMP, inhibiteurs potentiels de la biosynthèse des myco
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Romano, Domenico. "Synthesis of novel ribose-based thioimidate n-oxides." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amslaurea.unibo.it/10032/.

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This work is based on the study of new synthetic paths to obtain thioimidate N-oxides (TINOs) from D-ribose and to study their reactivity with the purpose to obtain ketonitrones. TINOs, aren’t well known molecules, but these enantiomerically pure backbones could be valuable intermediates in the synthesis of novel ketonitrones which are key intermediates in the synthesis of iminosugars. TINOs were discovered from the study of glucoraphanin, a particular glucosinolate, that unexpectedly cyclized into a TINO after desulfatation, by a spontaneous intramolecular Michael addition. The first part of
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Ostache, Nicu-Carmin. "Synthèse et fonctionnalisation de bicycles 5-5 polyazotés : pyrazolo[3,4-d]thiazoles et pyrazolo[3,4-c]pyrazoles." Thesis, Orléans, 2019. http://intranet.univ-orleans.fr/bibliotheques/theses/nicu-cosmin-ostache_3378_vm.pdf/.

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Les structures bicycliques azotées sont parmi les entités les plus utilisées dans le domaine thérapeutique.Les bicycles 5:5 polyazotés sont des structures moins décrites que leurs analogues 6:6 ou6:5. Malgré le potentiel pharmacologique des pyrazolo [3,4-d] thiazoles et des pyrazolo [3,4-c] pyrazoles,deux exemples de ces familles rares, seuls quelques procédés de préparation et de fonctionnalisationdirecte de ces charpentes hétérocycliques sont décrits.De ce fait, l’objectif principal de nos recherches vise à développer de nouvelles voies de synthèse vers cesdeux charpentes bicycliques et ce,
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Prieur, Vanessa. "Pyrrolo[2,3-d]pyrimidines : conception, synthèse, fonctionnalisation." Thesis, Orléans, 2015. http://www.theses.fr/2015ORLE2072/document.

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Les pyrrolo[2,3-d]pyrimidines, également connues sous le nom de 7-déazapurines, sont une classe importante d’hétérocycliques aromatiques, de par leurs potentiels biologiques (antitumoral, antiinflammatoire, antibactérien, etc.). C’est pourquoi ce squelette a été une source d’intérêt pour les chimistes organiciens. Outre leurs atouts biologiques, ces molécules présentent également de remarquables propriétés physico-chimiques (fluorescence UV), ce qui permet de nouvelles applications en électronique. Bien que ces dernières années, un bon nombre de recherche ont été mises en oeuvre en vue de synt
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Chany, Anne-Caroline. "Synthèse d'analogues des mycolactones, toxines de l'ulcère de Buruli." Thesis, Mulhouse, 2011. http://www.theses.fr/2011MULH4076.

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L'ulcère de Buruli est une maladie nécrosante de la peau et des tissus mous accompagnée d'ulcères de grandes tailles, causée par une mycobactérie. L’Organisation Mondiale de la Santé a lancé en 1998 une initiative mondiale contre cette maladie tropicale négligée, présente notamment en Afrique et en Australie. L'infection est causée par Mycobacterium ulcerans, mycobactérie faisant partie de la même famille que les mycobactéries responsables de la tuberculose et de la lèpre. Mycobacterium ulcerans sécrète une toxine nommée mycolactone, responsable de cette infection. Cette toxine a des propriété
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Book chapters on the topic "Liebeskind-Srogl"

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Li, Jie Jack. "Liebeskind-Srogl coupling." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_165.

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Li, Jie Jack. "Liebeskind-Srogl coupling." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_176.

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"55. Liebeskind–Srogl Cross Coupling." In Organic Chemistry: 100 Must-Know Mechanisms. De Gruyter, 2020. http://dx.doi.org/10.1515/9783110608373-055.

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Conference papers on the topic "Liebeskind-Srogl"

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Česnek, Michal, Petra Břehová, Martin Dračínský, Antonín Holý, and Zlatko Janeba. "The efficient synthesis of 2-aryl substituted pyrimidine acyclic nucleoside phosphonates using Liebeskind-Srogl cross-coupling." In XVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112310.

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Journal articles
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