Jorge L. O. Domingos

Author

Universidade Federal do Rio de Janeiro ORCID

Also Known As

Jorge Domingos, Jorge L. O. Domingos, Jorge L. de O. Domingos, Jorge L. de Oliveira Domingos, Jorge L.O Domingos, Jorge L.O. Domingos, Jorge Luiz O. Domingos, Jorge Luiz de Oliveira Domingos

Publications

205

Citations

H-Index

Concepts

All Affiliations

Universidade Federal do Rio de Janeiro Universidade do Estado do Rio de Janeiro University of Alicante

About

Jorge L. O. Domingos is an author at Universidade Federal do Rio de Janeiro specializing in pharmacology, organic chemistry, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	72
2	Engineering	2	2	22
3	Natural Sciences	2	2	29
4	Biochemistry	1	1	21
5	Biomolecular Engineering	1	1	10

Jorge L. O. Domingos

Publications

173

Citations

H-Index

Page 1

	Year	Citations
New hydrazides derivatives of isoniazid against Mycobacterium tuberculosis: Higher potency and lower hepatocytotoxicity Frederico Silva Castelo Branco, E.C.D. Lima, Jorge L. O. Domingos, European Journal of Medicinal Chemistry Pulmonary TuberculosisPharmaceutical ScienceHigher PotencyMedicineMycobacterium Tuberculosis	2018	41
Asymmetric Transfer Hydrogenation of Arylidene-Substituted Chromanones and Tetralones Catalyzed by Noyori–Ikariya Ru(II) Complexes: One-Pot Reduction of C═C and C═O bonds Guilherme S. Caleffi, Juliana de Oliveira Carneiro Brum, Angela T. Costa, The Journal of Organic Chemistry	2021	41
Synthesis and biological evaluation of α-aryl-α-tetralone derivatives as hepatitis C virus inhibitors Dinesh Manvar, Talita de A. Fernandes, Jorge L. O. Domingos, European Journal of Medicinal Chemistry BiochemistryMedicineAntiviral Drug DevelopmentAntiviral TherapyPharmacotherapy	2015	21
Stereoselective preparation of pyrrolidin-2-ones from a Z-enoate derived from d-(+)-mannitol Jorge L. O. Domingos, E.C.D. Lima, Ayres G. Dias, Tetrahedron Asymmetry Bioorganic ChemistryNatural SciencesOrganic ChemistryStereoselective PreparationStereoselective Synthesis	2004	18
Synthesis of 5‐Carbapterocarpens by α‐Arylation of Tetralones Followed by One‐Pot Demethylation/Cyclization with BBr<sub>3</sub> Talita de A. Fernandes, Jorge L. O. Domingos, Luiza I. A. da Rocha, European Journal of Organic Chemistry Cyclization SequenceEstrogenic ActivityDerivativesEngineeringNatural Sciences	2013	11
Enantioselective electrophilic fluorination of α-aryl-tetralones using a preparation of N-fluoroammonium salts of cinchonine Luana G. de Souza, Jorge L. O. Domingos, Talita de A. Fernandes, Journal of Fluorine Chemistry Chemical EngineeringEngineeringN-fluoroammonium SaltsFluorous SynthesisOrganic Chemistry	2018	11
Crude<i>D</i>‐(+)‐Glyceraldehyde Obtained from<i>D</i>‐Mannitol‐Diacetonide by Oxidative Cleavage with Sodium Periodate: Its Reactions with Nucleophilic Species Jorge L. O. Domingos, Guilherme V. M. de A. Vilela, Paulo R. R. Costa, Synthetic Communications	2004	10
Palladium-Catalyzed Oxyarylation, Azaarylation and &#945;-Arylation Reactions in the Synthesis of Bioactive Isoflavonoid Analogues Camilla D. Buarque, Jorge L. O. Domingos, Chaquip D. Netto, Current Organic Synthesis	2015	10
Synthesis of new α-Aryl-α-tetralones and α-Fluoro-α-aryl-α-tetralones, preliminary antiproliferative evaluation on drug resistant cell lines and in silico prediction of ADMETox properties Luana G. de Souza, Eduardo J. Salustiano, Kelli Monteiro da Costa, Bioorganic Chemistry Silico PredictionMedicinal ChemistryNatural Product SynthesisNew α-Aryl-α-tetralonesDrug Discovery	2021	10

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