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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A palladium/chiral amine co-catalyzed enantioselective dynamic cascade reaction: synthesis of polysubstituted carbocycles with a quaternary carbon stereocenter.
Guang-Ning Ma,Samson Afewerki,Luca Deiana,Carlos Palo-Nieto,Leifeng Liu,Junliang Sun,Ismail Ibrahem,Armando Córdova,Armando Córdova +8 more
TL;DR: Polysubstituted 5- and 6-membered carbocycles were synthesized by the title reaction by using a simple combination of palladium and chiral amine co-catalysts.
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Direct enantioselective synthesis of bicyclic Diels–Alder products
TL;DR: In this paper, a simple diamine catalyzes the asymmetric Diels-Alder reaction with high stereoselectivity and furnishes the corresponding Diels−Alder adducts in good to high yields with >25:1 dr and up to 86% ee.
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Combined heterogeneous metal/chiral amine: multiple relay catalysis for versatile eco-friendly synthesis.
Luca Deiana,Yan Jiang,Carlos Palo-Nieto,Samson Afewerki,Celia A. Incerti-Pradillos,Oscar Verho,Cheuk-Wai Tai,Eric V. Johnston,Armando Córdova +8 more
TL;DR: A versatile and broad synergistic strategy for expansion of chemical space and the synthesis of valuable molecules (e.g. carbocycles and heterocycles) using integrated heterogeneous metal/chiral amine multiple relay catalysis and air/O₂ as the terminal oxidant is described.
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Highly enantioselective organocatalytic addition of unmodified aldehydes to N-Boc protected imines: one-pot asymmetric synthesis of β-amino acids
TL;DR: Highly enantioselective catalytic routes to Boc protected?-amino aldehydes, amino acids and amino alcohols are presented in this paper.
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Organocatalytic asymmetric 5-hydroxypyrrolidine synthesis: a highly enantioselective route to 3-substituted proline derivatives
TL;DR: Organocatalytic asymmetric 5-hydroxypyrrolidine synthesis: a highly enantioselective route to 3-substituted proline derivatives.