General Synthesis Route to Benanomicin‐Pradimicin Antibiotics - Tamiya - 2007 - Chemistry – A European Journal - Wiley Online Library
Miguel MAESTRO | Professor (Full) | Química Organica | University of A Coruña, A Coruña | UDC | Department of Chemistry-CICA | Research profile
Versatile Friedelâ•fiCraftsâ•'Type Alkylation of Benzene Derivatives Using a Molybdenum Complex/<i>ortho</i>
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Highly regioselective synthesis of 2,3-disubstituted 2H-1-benzopyrans: Brønsted acid catalyzed [4+2] cycloaddition reaction with a variety of arylalkynes via ortho-quinone methides - ScienceDirect
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Phase Transition, Dielectric Properties, and Ionic Transport in the [(CH3)2NH2]PbI3 Organic–Inorganic Hybrid with 2H-Hexagonal Perovskite Structure | Inorganic Chemistry
Appendix I: DUPONT BY THE CASTLE BUSINESS IMPROVEMENT AREA Financial Statements Year Ended December 31, 2014
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Vermellogens” and the Development of CB[8]-Based Supramolecular Switches Using pH-Responsive and Non-Toxic Viologen Analogues | Journal of the American Chemical Society
![Highly regioselective synthesis of 2,3-disubstituted 2H-1-benzopyrans: Brønsted acid catalyzed [4+2] cycloaddition reaction with a variety of arylalkynes via ortho-quinone methides - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S004040201730981X-sc4.jpg "Highly regioselective synthesis of 2,3-disubstituted 2H-1-benzopyrans: Brønsted acid catalyzed [4+2] cycloaddition reaction with a variety of arylalkynes via ortho-quinone methides - ScienceDirect")
Highly regioselective synthesis of 2,3-disubstituted 2H-1-benzopyrans: Brønsted acid catalyzed [4+2] cycloaddition reaction with a variety of arylalkynes via ortho-quinone methides - ScienceDirect
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Highly regioselective synthesis of 2,3-disubstituted 2H-1-benzopyrans: Brønsted acid catalyzed [4+2] cycloaddition reaction with a variety of arylalkynes via ortho-quinone methides - ScienceDirect
Effects of mordenite zeolite catalyst synthesis conditions on dimethyl ether carbonylation - ScienceDirect
Catalysts | Free Full-Text | Evaluation of ·OH Production Potential of Particulate Matter (PM2.5) Collected on TiO2-Supporting Quartz Filters
Catalysts | Free Full-Text | Modeling the OEC with Two New Biomimetic Models: Preparations, Structural Characterization, and Water Photolysis Studies of a Ba–Mn Box Type Complex and a Mn4N6 Planar-Diamond Cluster
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Midnight Sun - Walking Circles (1972) [CLOCKWORK PEACH]
Preferential SOx Adsorption in Mg-MOF-74 from a Humid Acid Gas Stream | ACS Applied Materials & Interfaces
Catalysts | Free Full-Text | Evaluation of ·OH Production Potential of Particulate Matter (PM2.5) Collected on TiO2-Supporting Quartz Filters
Catalysts | Free Full-Text | Evaluation of ·OH Production Potential of Particulate Matter (PM2.5) Collected on TiO2-Supporting Quartz Filters
Versatile Friedel–Crafts‐Type Alkylation of Benzene Derivatives Using a Molybdenum Complex/ortho‐Chloranil Catalytic System - Yamamoto - 2008 - Chemistry – A European Journal - Wiley Online Library
Catalysts | Free Full-Text | Evaluation of ·OH Production Potential of Particulate Matter (PM2.5) Collected on TiO2-Supporting Quartz Filters
![Highly regioselective synthesis of 2,3-disubstituted 2H-1-benzopyrans: Brønsted acid catalyzed [4+2] cycloaddition reaction with a variety of arylalkynes via ortho-quinone methides - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S004040201730981X-fx1.jpg "Highly regioselective synthesis of 2,3-disubstituted 2H-1-benzopyrans: Brønsted acid catalyzed [4+2] cycloaddition reaction with a variety of arylalkynes via ortho-quinone methides - ScienceDirect")
Highly regioselective synthesis of 2,3-disubstituted 2H-1-benzopyrans: Brønsted acid catalyzed [4+2] cycloaddition reaction with a variety of arylalkynes via ortho-quinone methides - ScienceDirect
Hydroxymethyl Rotamer Populations in Disaccharides | The Journal of Organic Chemistry
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Vermellogens” and the Development of CB[8]-Based Supramolecular Switches Using pH-Responsive and Non-Toxic Viologen Analogues | Journal of the American Chemical Society
Disociación y ácidos bases
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Vermellogens” and the Development of CB[8]-Based Supramolecular Switches Using pH-Responsive and Non-Toxic Viologen Analogues | Journal of the American Chemical Society
Molecules | January-2 2020 - Browse Articles
