Highly Diastereoselective Multicomponent Synthesis of Spirocyclopropyl Oxindoles Enabled by Rare-Earth Metal Salts
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A. Poveda | G. Jiménez‐Osés | P. Costanzo | L. Maiuolo | Vincenzo Algieri | C. D. Navo | F. Olivito | A. De Nino | M. A. Tallarida | Antonio Jiritano | J. Jiménez‐Barbero | M. J. Moure | Claudio D. Navo | Gonzalo Jiménez‐Osés
[1] Jian Wu,et al. Spiro Derivatives in the Discovery of New Pesticides: A Research Review. , 2022, Journal of agricultural and food chemistry.
[2] W. Evans,et al. A Rare-Earth Metal Retrospective to Stimulate All Fields. , 2021, Journal of the American Chemical Society.
[3] T. Boyle,et al. Solvation coordination compounds of scandium chloride from the dehydration of scandium chloride hexahydrate , 2021 .
[4] S. Murugesan,et al. Oxindole and its derivatives: A review on recent progress in biological activities. , 2021, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[5] A. Burke,et al. Engaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversity , 2021, Chemical record.
[6] Wenchao Yang,et al. Where are the New Herbicides? , 2021, Pest management science.
[7] A. Burke,et al. The application of isatin-based multicomponent-reactions in the quest for new bioactive and druglike molecules. , 2020, European journal of medicinal chemistry.
[8] Hafiza Amna Younus,et al. Multicomponent reactions (MCR) in medicinal chemistry: a patent review (2010-2020) , 2020, Expert opinion on therapeutic patents.
[9] R. Anwander,et al. Carbonyl group and carbon dioxide activation by rare-earth-metal complexes. , 2020, Dalton transactions.
[10] Akash P Sakla,et al. Syntheses and Applications of Spirocyclopropyl Oxindoles: A Decade Review , 2020 .
[11] Lin Chen,et al. DABCO-Catalyzed Michael/Alkylation Cascade Reactions Involving α-Substituted Ammonium Ylides for the Construction of Spirocyclopropyl Oxindoles: Access to the Powerful Chemical Leads against HIV-1. , 2020, The Journal of organic chemistry.
[12] P. Merino,et al. Synthesis, Biological and In Silico Evaluation of Pure Nucleobase-Containing Spiro (Indane-Isoxazolidine) Derivatives as Potential Inhibitors of MDM2–p53 Interaction , 2019, Molecules.
[13] M. D. Di Gioia,et al. Regioselective synthesis of 1,5-disubstituted 1,2,3-triazoles by 1,3-dipolar cycloaddition: Role of Er(OTf)3, ionic liquid and water , 2019, Tetrahedron Letters.
[14] Lili Lin,et al. Catalytic Asymmetric Ring-Opening/Cyclopropanation of Cyclic Sulfur Ylides: Construction of Sulfur-Containing Spirocyclopropyloxindoles with Three Vicinal Stereocenters. , 2018, Organic letters.
[15] H. Ko,et al. Synthesis of Spiro[oxindole-3,2'-pyrrolidine] Derivatives from Benzynes and Azomethine Ylides through 1,3-Dipolar Cycloaddition Reactions. , 2018, The Journal of organic chemistry.
[16] Linfeng Hu,et al. Catalytic Asymmetric Synthesis of Chiral Spiro‐cyclopropyl Oxindoles from 3‐Alkenyl‐oxindoles and Sulfoxonium Ylides , 2018, Advanced Synthesis & Catalysis.
[17] Guang-Jian Mei,et al. Catalytic asymmetric synthesis of spirooxindoles: recent developments. , 2018, Chemical communications.
[18] P. Merino,et al. Nitrones and nucleobase-containing spiro-isoxazolidines derived from isatin and indanone: solvent-free microwave-assisted stereoselective synthesis and theoretical calculations , 2017 .
[19] Lili Lin,et al. Asymmetric Cycloaddition and Cyclization Reactions Catalyzed by Chiral N,N'-Dioxide-Metal Complexes. , 2017, Accounts of chemical research.
[20] M. Gioia,et al. Selective Acetylation of Small Biomolecules and Their Derivatives Catalyzed by Er(OTf)3 , 2017 .
[21] K. P. Kepp. A Quantitative Scale of Oxophilicity and Thiophilicity. , 2016, Inorganic chemistry.
[22] C. Hulme,et al. Recent Advances in Multicomponent Reaction Chemistry , 2015 .
[23] Hong-min Liu,et al. Spirooxindoles: Promising scaffolds for anticancer agents. , 2015, European journal of medicinal chemistry.
[24] Narendra Kumar Patel,et al. The discovery of Polo-like kinase 4 inhibitors: design and optimization of spiro[cyclopropane-1,3'[3H]indol]-2'(1'H).ones as orally bioavailable antitumor agents. , 2015, Journal of medicinal chemistry.
[25] Chaoguo Yan,et al. Molecular diversity of cycloaddition reactions of the functionalized pyridinium salts with 3-phenacylideneoxindoles , 2013 .
[26] Jian Zhou,et al. Highly stereoselective olefin cyclopropanation of diazooxindoles catalyzed by a C2-symmetric spiroketal bisphosphine/Au(I) complex. , 2013, Journal of the American Chemical Society.
[27] Yunyun Liu,et al. Recent Advances in Diversity Oriented Synthesis through Isatin-based Multicomponent Reactions , 2013 .
[28] Yixin Lu,et al. Diastereodivergent synthesis of 3-spirocyclopropyl-2-oxindoles through direct enantioselective cyclopropanation of oxindoles. , 2012, Chemistry.
[29] K. Shih,et al. Kinetics and mechanism of propachlor reductive transformation through nucleophilic substitution by dithionite. , 2011, Chemosphere.
[30] A. Mazzanti,et al. Organocatalytic Michael-alkylation cascade: the enantioselective nitrocyclopropanation of oxindoles. , 2011, Chemistry.
[31] J. Caldwell,et al. Design, synthesis, and biological evaluations of novel oxindoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. Part 2. , 2006, Bioorganic & medicinal chemistry letters.
[32] S. Hirano,et al. Exposure, metabolism, and toxicity of rare earths and related compounds. , 1996, Environmental health perspectives.
[33] G. Choppin,et al. Lanthanide(III) trifluoromethanesulfonate complexes in anhydrous acetonitrile , 1993 .
[34] A. Franz,et al. Recent advances in organocatalytic asymmetric multicomponent cascade reactions for enantioselective synthesis of spirooxindoles , 2021 .
[35] J. Caldwell,et al. Design, synthesis and biological evaluations of novel oxindoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. Part I. , 2006, Bioorganic & medicinal chemistry letters.