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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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Direct Organocatalytic Asymmetric Reductive Mannich-Type Reactions.

TL;DR: In this paper, a direct asymmetric reductive Manich-type reaction that allows for the formation of three contiguous stereocenters with high chemo-, diastereo-, and enantioselectivity is presented.
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Highly Enantioselective Synthesis of 2H-1-Benzothiopyrans by a Catalytic Domino Reaction.

TL;DR: In this paper, a highly enantioselective catalytic asymmetric synthesis of 2 H -1-benzothiopyrans was presented, which achieved high yields with 91-98% ee.
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Direct Amino Acid Catalyzed Asymmetric α Oxidation of Ketones with Molecular Oxygen.

TL;DR: The ability of amino acids to form nucleophilic enamines with aldehydes and ketones has been used in the development of asymmetric α-oxidation reactions with electrophilic oxidizing agents.
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Convenient Synthesis of L-Proline Benzyl Ester.

TL;DR: In this paper, it was shown that mesylates or tosylates of delta-hydroxy-L-norvaline esters spontaneously afford L-proline esters upon exposure to aqueous buffer in near quantitative yield.
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Off‐Cycle Catalyst Cooperativity in Amine/Transition Metal Combined Catalysis: Bicyclo[3.2.0]heptanes as Key Species in Co‐catalytic Enantioselective Carbocyclizations

TL;DR: The existence of off-cycle catalyst cooperativity in amine/metal combined catalysis is disclosed in this paper , where the experimental and density functional theory study of the amine and metal co-catalyzed enantioselective Michael/carbocyclization cascade reaction between allenes and α,β-unsaturated aldehydes reveals that the dual catalysts can perform off-cycled cooperativity that gives access to stable bicyclo[3.2.0]heptane species that limits the carbocycle product formation.