About: Armando Córdova

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researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Armando Córdova (en) Armando Córdova (es) Armando Córdova (nl) Armando Córdova (ast)
skos:prefLabel	Armando Córdova (en) Armando Córdova (es) Armando Córdova (nl) Armando Córdova (ast)
name	Armando Córdova (en) Armando Córdova (es) Armando Córdova (nl) Armando Córdova (ast)
Scopus author ID	wds:Q43897570-E64B669E-B9C6-41D4-A772-458B642A0CD4
Scopus author ID	7006135350
given name	wds:Q43897570-B9D38CB9-2525-4647-A811-43C454C61B85
given name	Armando
instance of	wds:Q43897570-BC28F995-1FB1-434D-B5FB-C3C52EAA3258
instance of	Homo sapiens
IxTheo authority ID	wds:Q43897570-4E6EB156-2A12-4D8D-9B79-D06027D87888
occupation	wds:Q43897570-A613E08D-2FE2-4B5A-B3CE-DCAE3E333EB0
sex or gender	wds:Q43897570-D75C01A8-099A-4D4F-BB24-A081BE35896E
VIAF ID	wds:Q43897570-28067158-F349-4F24-BD7D-26F10C8A295B
GND ID	wds:Q43897570-c1200f95-52cf-491e-9221-34453a81ecbd
family name	wds:Q43897570-1B31AA12-7984-450D-89DE-5D57AFB5E406
WorldCat Identities ID (superseded)	wds:Q43897570-30950775-098A-49D1-A2A3-51EC51FAD412
Kallías ID	wds:Q43897570-D9B705E8-E125-47A9-BAFE-2B6942258F90
VIAF ID	http://viaf.org/viaf/205918277
GND ID	https://d-nb.info/gnd/170537668
IxTheo authority ID	06064141X
occupation	researcher
sex or gender	male
VIAF ID	205918277
GND ID	170537668
family name	Córdova
WorldCat Identities ID (superseded)	viaf-205918277
Kallías ID	PE00454204
ORCID iD	wds:Q43897570-5B6753A6-9CCC-4C20-B8BB-1B23C5BDC22C
ORCID iD	https://orcid.org/0000-0001-9620-8698
ORCID iD	0000-0001-9620-8698
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q43897570
is author of	Direct amino acid catalyzed asymmetric alpha oxidation of ketones with molecular oxygen The direct amino acid-catalyzed asymmetric incorporation of molecular oxygen to organic compounds. Inorganic ammonium salts and carbonate salts are efficient catalysts for aldol condensation in atmospheric aerosols. Direct organocatalytic aldol reactions in buffered aqueous media A highly enantioselective route to either enantiomer of both alpha- and beta-amino acid derivatives The direct catalytic asymmetric mannich reaction. Catalytic enantioselective β-alkylation of α,β-unsaturated aldehydes by combination of transition-metal- and aminocatalysis: total synthesis of bisabolane sesquiterpenes. Proline-catalyzed one-step asymmetric synthesis of 5-hydroxy-(2E)-hexenal from acetaldehyde. Acyclic chiral amines and amino acids as inexpensive and readily tunable catalysts for the direct asymmetric three-component Mannich reaction Plausible origins of homochirality in the amino acid catalyzed neogenesis of carbohydrates Direct catalytic enantioselective aza-Diels-Alder reactions A highly enantioselective amino acid-catalyzed route to functionalized alpha-amino acids The Direct catalytic asymmetric cross-Mannich reaction: a highly enantioselective route to 3-amino alcohols and alpha-amino acid derivatives The direct catalytic asymmetric alpha-aminooxylation reaction: development of stereoselective routes to 1,2-diols and 1,2-amino alcohols and density functional calculations Acyclic amino acid-catalyzed direct asymmetric aldol reactions: alanine, the simplest stereoselective organocatalyst. Small peptides as modular catalysts for the direct asymmetric aldol reaction: ancient peptides with aldolase enzyme activity A concise enantioselective synthesis of iminosugar derivatives. One-Pot Asymmetric Synthesis of β-Cyanohydroxymethyl α-Amino Acid Derivatives: Formation of Three Contiguous Stereogenic Centers Direct organocatalytic enantioselective α-aminomethylation of ketones Direct catalytic enantioselective alpha-aminomethylation of ketones. Direct catalytic enantioselective alpha-aminoxylation of ketones: a stereoselective synthesis of alpha-hydroxy and alpha,alpha'-dihydroxy ketones Direct catalytic enantioselective alpha-aminomethylation of aldehydes Simple highly modular acyclic amine-catalyzed direct enantioselective addition of ketones to nitro-olefins Direct catalytic intermolecular alpha-allylic alkylation of aldehydes by combination of transition-metal and organocatalysis Direct catalytic asymmetric anti-selective Mannich-type reactions Products and kinetics of the liquid-phase reaction of glyoxal catalyzed by ammonium ions (NH4(+)). Organocatalytic enantioselective aminosulfenylation of alpha,beta-unsaturated aldehydes Direct amino acid catalyzed asymmetric synthesis of polyketide sugars Amino acid catalyzed neogenesis of carbohydrates: a plausible ancient transformation The origin of stereoselectivity in primary amino acid catalyzed intermolecular aldol reactions The small peptide-catalyzed direct asymmetric aldol reaction in water Organocatalytic enantioselective aziridination of alpha,beta-unsaturated aldehydes Organocatalytic asymmetric 5-hydroxyisoxazolidine synthesis: a highly enantioselective route to beta-amino acids Dynamic kinetic asymmetric domino oxa-Michael/carbocyclization by combination of transition-metal and amine catalysis: catalytic enantioselective synthesis of dihydrofurans Catalytic asymmetric aziridination of α,β-unsaturated aldehydes Direct regiospecific and highly enantioselective intermolecular α-allylic alkylation of aldehydes by a combination of transition-metal and chiral amine catalysts. One-pot three-component catalytic enantioselective synthesis of homoallylboronates. Catalytic enantioselective domino oxa-michael/aldol condensations: asymmetric synthesis of benzopyran derivatives One-pot catalytic asymmetric cascade synthesis of cycloheptane derivatives. Enantioselective organocatalytic conjugate addition of fluorocarbon nucleophiles to alpha,beta-unsaturated aldehydes. A palladium/chiral amine co-catalyzed enantioselective dynamic cascade reaction: synthesis of polysubstituted carbocycles with a quaternary carbon stereocenter. Highly enantioselective organocatalytic addition of aldehydes to N-(Phenylmethylene)benzamides: asymmetric synthesis of the paclitaxel side chain and its analogues One-pot catalytic enantioselective domino nitro-michael/michael synthesis of cyclopentanes with four stereocenters

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