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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Lipase-catalyzed synthesis of methyl 6-O-poly(ε-caprolactone)glycopyranosides
TL;DR: In this paper, an enzymatic approach to combine ring-opening polymerization of e-caprolactone and regioselective acylation of methyl glycopyranosides has been investigated.
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Enantioselective organocatalytic conjugate addition of fluorocarbon nucleophiles to α,β-unsaturated aldehydes
Farman Ullah,Gui-Ling Zhao,Luca Deiana,Mingzhao Zhu,Pawel Dziedzic,Ismail Ibrahem,Peter Hammar,Junliang Sun,Armando Córdova +8 more
TL;DR: A highly chemo- and enantioselective organocatalytic addition of fluorocarbon nucleophiles, such as 1-fluoro-bis(phenylsulfonyl)methane, toα,β-unsaturated aldehydes is presented to give access to optically active fluorine derivatives in good yields and up to 95 % ee.
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Amino acid-catalyzed direct enantioselective synthesis of β-amino-α-oxyaldehydes
Ismail Ibrahem,Armando Córdova +1 more
TL;DR: The first direct amino acid-catalyzed asymmetric syntheses of α-oxy-β-aminoaldehydes are presented and the corresponding α-aldehyde adducts were isolated in high yield with excellent chemo- and enantioselectivity.
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A simple one-pot, three-component, catalytic, highly enantioselective isoxazolidine synthesis
TL;DR: In this article, the highly chemo-and enanti-lective organocatalytic three-component reaction between N-arylhydroxylamines, aldehydes and?,?-unsaturated aldehyde is presented; the reaction gives access to isoxazolidines in high yields with >25:1 dr and 91-99% ee.
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Highly diastereo- and enantioselective catalytic domino thia-Michael/aldol reactions: synthesis of benzothiopyrans with three contiguous stereocenters
TL;DR: Highly diastereo and enantioselective catalytic domino thia-Michael/aldol reactions: Synthesis of benzothiopyrans with three contiguous stereocenters.