A
Armando Córdova
Researcher at Mid Sweden University
Publications - 311
Citations - 13750
Armando Córdova is an academic researcher from Mid Sweden University. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 68, co-authored 303 publications receiving 12969 citations. Previous affiliations of Armando Córdova include Scripps Research Institute & Stockholm University.
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Sugar‐Assisted Kinetic Resolution of Amino Acids and Amplification of Enantiomeric Excess of Organic Molecules
TL;DR: This work proposes and demonstrates a novel alternative for the evolution of homochirality that is not based on autocatalysis and forges a direct relationship between the chirality of sugars and amino acids.
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Silver-Triggered Activity of a Heterogeneous Palladium Catalyst in Oxidative Carbonylation Reactions.
Man-Bo Li,Man-Bo Li,Ying Yang,Abdolrahim Abbaszad Rafi,Michael Oschmann,Erik Svensson Grape,A. Ken Inge,Armando Córdova,Jan-Erling Bäckvall,Jan-Erling Bäckvall +9 more
TL;DR: A silver‐triggered heterogeneous Pd‐catalyzed oxidative carbonylation has been developed that exhibits high efficiency and good recyclability, and was utilized for the one‐pot construction of polycyclic compounds with multiple chiral centers.
Posted ContentDOI
Common inorganic ions are efficient catalysts for organic reactions in atmospheric aerosols and other natural environments
TL;DR: In this article, inorganic ammonium ions, NH4+, and carbonate ions, CO32−, are reported for the first time as catalysts for organic reactions in atmospheric aerosols and other natural environments at the Earth's surface.
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Efficient and Highly Enantioselective Aerobic Oxidation–Michael–Carbocyclization Cascade Transformations by Integrated Pd(0)-CPG Nanoparticle/Chiral Amine Relay Catalysis
TL;DR: The heterogeneous Pd(0)-CPG nanoparticle catalysts were efficient for both the sequential aerobic oxidation and dynamic kinetic asymmetric Michael–carbocyclization transformations, resulting in oxidation of a variety of allylic alcohols to enals and formation of cyclopentenes containing an all-carbon quaternary stereocenter in good to high yields.
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Concise Catalytic Asymmetric Total Synthesis of Biologically Active Tropane Alkaloids
TL;DR: In this article, a general strategy for the total asymmetric synthesis of valuable tropane alkaloids by catalytic stereoselective transformations is disclosed, and the power of this approach is exemplified by the conci...