Paulo Roberto Ribeiro Costa
Instituição:
Universidade Federal do Rio de Janeiro
Centro:
Centro de Ciências da Saúde
Unidade:
Instituto de Pesquisas de Produtos Naturais
Departamento:
Programa de Produtos Naturais/IPPN
Formação:
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Université Pierre et Marie Curie
| Pós-Doutorado | 1988 - 1988
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Université Joseph Fourier - Grenoble I
| Pós-Doutorado | 1988 - 1988
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Université Joseph Fourier - Grenoble I
| Pós-Doutorado | 1984 - 1984
-
Universidade Federal do Rio de Janeiro
Química | Doutorado | 1978 - 1983
-
Universidade Federal do Rio de Janeiro
Química de Produtos Naturais | Mestrado | 1972 - 1975
-
Universidade Federal do Rio de Janeiro
Faculdade de Farmácia | Graduação | 1969 - 1972
Laboratórios:
Nuvens de Palavras:
Artigos:
(85.00% artigos com DOI)
Titulo | DOI | Ano |
---|---|---|
Microarray data analysis of antileukemic action of Cinnamoylated benzaldehyde LQB-461 in Jurkat cell line | 10.1007/s11033-023-09030-y | 2024 |
Advances in the synthesis of rearranged homoisoflavonoids | 10.1039/d4ob00627e | 2024 |
Flavonoids as Inspiration for the Design and Synthesis of New Antiproliferative, Antiparasitic and Antiviral Compounds: An Account | 10.21577/0103-5053.20240056 | 2024 |
Flavonoids as Inspiration for the Design and Synthesis of New Antiproliferative, Antiparasitic and Antiviral Compounds: An Account | 10.21577/0103-5053.20240056 | 2024 |
Advances in the synthesis of rearranged homoisoflavonoids | 10.1039/D4OB00627E | 2024 |
Low doses of 3-phenyl-lawsone or meglumine antimoniate delivery by tattooing route are successful in reducing parasite load in cutaneous lesions of Leishmania (Viannia) braziliensis-infected hamsters | 10.3389/fcimb.2023.1025359 | 2023 |
Aurones: A Promising Scaffold to Inhibit SARS-CoV-2 Replication | 10.1021/acs.jnatprod.3c00249 | 2023 |
Deacylative Allylation Reaction: A promising Approach for the Synthesis of Compounds Containing the Allyl Group at Quaternary Centers | 10.21577/1984-6835.20230025 | 2023 |
LQB-118 Suppresses Migration and Invasion of Prostate Cancer Cells by Modulating the Akt/GSK3β Pathway and MMP-9/Reck Gene Expression | 10.21873/anticanres.16171 | 2023 |
Aurones: A Promising Scaffold to Inhibit SARS-CoV-2 Replication | 10.1021/acs.jnatprod.3c00249 | 2023 |
Low doses of 3-phenyl-lawsone or meglumine antimoniate delivery by tattooing route are successful in reducing parasite load in cutaneous lesions of Leishmania (Viannia) braziliensis-infected hamsters | 10.3389/fcimb.2023.1025359 | 2023 |
Asymmetric hydrogenation and transfer hydrogenation in the enantioselective synthesis of flavonoids | 10.1039/d1qo01503f | 2022 |
The Isoflavanoid (+)-PTC Regulates Cell-Cycle Progression and Mitotic Spindle Assembly in a Prostate Cancer Cell Line | 10.1002/cbdv.202200102 | 2022 |
Ru(II)-Catalyzed Asymmetric Transfer Hydrogenation of Chalcones in Water: Application to the Enantioselective Synthesis of Flavans BW683C and Tephrowatsin E | 10.1021/acs.joc.2c01733 | 2022 |
Effects of |
10.1002/ps.6900 | 2022 |
New 5-carba-pterocarpans: Synthesis and preliminary antiproliferative activity on a panel of human cancer cells | 10.1016/j.bioorg.2020.104584 | 2021 |
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 | 10.1016/j.bioorg.2021.104790 | 2021 |
The pterocarpanquinone LQB-118 compound induces apoptosis of cytarabine-resistant acute myeloid leukemia cells | 10.3892/ijo.2021.5204 | 2021 |
N - tert -Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles | 10.3762/bjoc.17.86 | 2021 |
The Potent Trypanocidal Effect of LQB303, a Novel Redox-Active Phenyl-Tert-Butyl-Nitrone Derivate That Causes Mitochondrial Collapse in Trypanosoma cruzi | 10.3389/fmicb.2021.617504 | 2021 |
Monocyclic Nitro-heteroaryl Nitrones with Dual Mechanism of Activation: Synthesis and Antileishmanial Activity | 10.1021/acsmedchemlett.1c00193 | 2021 |
Enantioselective synthesis of isoflavanones and pterocarpans through a RuII¿catalyzed ATH¿DKR of isoflavones | 10.1002/cctc.202101252 | 2021 |
Synthesis and Biological Evaluation of Cyclic Analogues from Nitrone LQB-278: A New Potential Antileukemia Compound | 10.21873/anticanres.15306 | 2021 |
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 | 10.1021/acs.joc.0c02981 | 2021 |
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 | 10.1016/j.bioorg.2021.104790 | 2021 |
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 | 10.1021/acs.joc.0c02981 | 2021 |
The Potent Trypanocidal Effect of LQB303, a Novel Redox-Active Phenyl-Tert-Butyl-Nitrone Derivate That Causes Mitochondrial Collapse in Trypanosoma cruzi | 10.3389/fmicb.2021.617504 | 2021 |
LQB-118 compound inhibits migration and induces cell death in glioblastoma cells | 10.3892/or.2019.7402 | 2020 |
The pterocarpanquinone LQB 118 inhibits inflammation triggered by zymosan in vivo and in vitro | 10.1016/j.intimp.2020.106399 | 2020 |
Theoretical studies and NMR assay of coumarins and neoflavanones derivatives as potential inhibitors of acetylcholinesterase | 10.1016/j.compbiolchem.2020.107293 | 2020 |
Synthesis of pterocarpans through palladium-catalyzed oxyarylation of alkoxy-2H-chromenes with o-iodophenols | 10.1016/j.tet.2020.131638 | 2020 |
Insights into the Biological Evaluation of Pterocarpanquinones and Carbapterocarpans with Anti-Tumor Activity against MDR Leukemias | 10.2174/1871520618666180420165128 | 2019 |
Enantioselective Synthesis, DFT Calculations, and Preliminary Antineoplastic Activity of Dibenzo 1-Azaspiro[4.5]decanes on Drug-Resistant Leukemias | 10.1021/acs.joc.8b03203 | 2019 |
Lapachol and synthetic derivatives: in vitro and in vivo activities against Bothrops snake venoms | 10.1371/journal.pone.0211229 | 2019 |
Enantioselective electrophilic fluorination of α-aryl-tetralones using a preparation of N-fluoroammonium salts of cinchonine | 10.1016/j.jfluchem.2018.11.007 | 2019 |
Switching Diastereoselectivity in Catalytic Enantioselective (3+2) Cycloadditions of Azomethine Ylides Promoted by Metal Salts and Privileged Segphos-Derived Ligands | 10.1021/acs.joc.9b00267 | 2019 |
The LQB-223 Compound Modulates Antiapoptotic Proteins and Impairs Breast Cancer Cell Growth and Migration | 10.3390/ijms20205063 | 2019 |
Snake venom activities as a tool to develop new metalloproteinase inhibitors from synthetic derivatives of lapachol | 10.1016/j.toxicon.2019.06.133 | 2019 |
Medicinal Electrochemistry of Halogenated and Nitrated Pterocarpanquinones | 10.21577/0103-5053.20190161 | 2019 |
Insights into the Biological Evaluation of Pterocarpanquinones and Carbapterocarpans with Anti-tumor Activity against MDR Leukemias | 10.2174/1871520618666180420165128 | 2019 |
The orally active pterocarpanquinone LQB-118 exhibits cytotoxicity in prostate cancer cell and tumor models through cellular redox stress | 10.1002/pros.23455 | 2018 |
New Palladacycle-Derived Acylhydrazones as Pre-catalysts in Mirozoki-Heck Coupling and Oxyarylations | 10.1590/0001-3765201820170858 | 2018 |
Second-generation pterocarpanquinones: synthesis and antileishmanial activity | 10.1186/s40409-018-0174-7 | 2018 |
11a- N -tosyl-5-carbapterocarpans: synthesis, antineoplastic evaluation and in silico prediction of ADMETox properties | 10.1016/j.bioorg.2018.07.004 | 2018 |
Interaction between bioactive compound 11a-N-tosyl-5-deoxi-pterocarpan (LQB-223) and Calf thymus DNA: Spectroscopic approach, electrophoresis and theoretical studies | 10.1016/j.ijbiomac.2016.12.044 | 2017 |
Preparative chiral separation and absolute configuration of the synthetic pterocarpanquinone LQB-118 | 10.1002/chir.22696 | 2017 |
Solvent-Free Synthesis of Salen Ligands and Pd(II)- and Cu(II)-Salen Complexes: Their Use in the Oxidation of α-Tetralones to α-Naphthols | 10.1055/s-0036-1588446 | 2017 |
Palladium-Catalyzed α-Arylation of Dimethyl Malonate and Ethyl Cyanoacetate with o-Alkoxybromobenzenes for the Synthesis of Phenylacetic Acid, Esters and Phenylacetonitriles | 10.1055/s-0036-1588550 | 2017 |
Mutagenic and Cytotoxicity LQB 123 Profile: Safety and Tripanocidal Effect of a Phenyl-t-Butylnitrone Derivative | 10.1155/2017/2483652 | 2017 |
Bifunctional primary amine 2-aminobenzimidazole organocatalyst anchored to trans-cyclohexane-1,2-diamine in enantioselective conjugate additions of aldehydes | 10.1016/j.tetasy.2015.12.004 | 2016 |
5-Carba-pterocarpens: A New Scaffold with Anti-HCV Activity | 10.1016/j.ejmech.2016.02.010 | 2016 |
Preclinical Studies Evaluating Subacute Toxicity and Therapeutic Efficacy of LQB-118 in Experimental Visceral Leishmaniasis | 10.1128/aac.01787-15 | 2016 |
Antileishmanial Activity of Ezetimibe: Inhibition of Sterol Biosynthesis, In Vitro Synergy with Azoles, and Efficacy in Experimental Cutaneous Leishmaniasis | 10.1128/aac.01545-16 | 2016 |
In vitro and in vivo antineoplastic and immunological effects of pterocarpanquinone LQB-118 | 10.1007/s10637-016-0359-2 | 2016 |
Reactive Oxygen Species Release, Alkylating Ability, and DNA Interactions of a Pterocarpanquinone: A Test Case for Electrochemistry | 10.1002/celc.201600504 | 2016 |
Anti-inflammatory properties of pterocarpanquinone LQB-118 in mice | 10.1016/j.bmc.2016.07.046 | 2016 |
The syn-selective conjugate addition of amines to enoates derived from d-mannitol | 10.1016/j.tetasy.2016.06.017 | 2016 |
Copper-versus palladium-catalyzed aromatization of 2-(methoxycarbonyl) tetralones: synthesis of methyl 1-hydroxy-2-naphthoates | 10.1016/j.tet.2016.01.057 | 2016 |
Non-competitive inhibitor of nucleoside hydrolase from Leishmania donovani identified by fragment-based drug discovery | 10.1039/c6ra15143d | 2016 |
Suzuki-Miyaura Coupling between 3-Iodolawsone and Arylboronic Acids. Synthesis of Lapachol Analogues with Antineoplastic and Antileishmanial Activities | 10.21577/0103-5053.20160326 | 2016 |
Synthesis and biological evaluation of α-aryl-α-tetralone derivatives as hepatitis C virus inhibitors | 10.1016/j.ejmech.2015.01.057 | 2015 |
NFκB Pathway and microRNA-9 and -21 are Involved in Sensitivity to the Pterocarpanquinone LQB-118 in Different CML Cell Lines | 10.2174/18715206113139990108 | 2015 |
Palladium-Catalyzed Oxyarylation, Azaarylation and α-Arylation Reactions in the Synthesis of Bioactive Isoflavonoid Analogues | 10.2174/157017941206150828112502 | 2015 |
Abstract A51: Antineoplastic activity of novel synthetic compound pterocarpanquinone LQB-118 in lung cancer cells | 10.1158/1557-3265.PMS14-A51 | 2015 |
Abstract A49: Efficiency of 11a-N-tosyl-5-deoxi-pterocarpan (LQB-223) in a panel of myeloid leukemia cell lines with different chemoresistance backgrounds | 10.1158/1557-3265.PMS14-A49 | 2015 |
Synthesis of N-methylarylnitrones derived from alkyloxybenzaldehydes and antineoplastic effect on human cancer cell lines | 10.1016/j.bmc.2015.03.014 | 2015 |
Synthesis of Chromen[4,3- b ]pyrrolidines by Intramolecular 1,3-Dipolar Cycloadditions of Azomethine Ylides: An Experimental and Computational Assessment of the Origin of Stereocontrol | 10.1002/ejoc.201500434 | 2015 |
Synthesis of 11a-N-Arylsulfonyl-5-carbapterocarpans (Tetrahydro-5H-benzo[a]carbazoles) by Azaarylation of Dihydronaphthalenes with o-Iodo-N-(Arylsulfonyl)anilines in Poly(ethylene glycol) | 10.1055/s-0034-1380757 | 2015 |
Ligand-Free Palladium-Catalyzed Oxyarylation of Dihydronaphthalenes and Chromenequinone with o-Iodophenols and 3-Iodolawsone in PEG-400: An Efficient Synthesis of 5-Carbapterocarpans and Pterocarpanquinones | 10.1055/s-0034-1378745 | 2015 |
Further evidence that naphthoquinone inhibits Toxoplasma gondii growth in vitro | 10.1016/j.parint.2015.08.010 | 2015 |
Synthesis of 5-Carbapterocarpens by α-Arylation of Tetralones Followed by One-Pot Demethylation/Cyclization with BBr 3 | 10.1002/ejoc.201301505 | 2014 |
The pterocarpanquinone LQB-118 induces apoptosis in acute myeloid leukemia cells of distinct molecular subtypes and targets FoxO3a and FoxM1 transcription factors | 10.3892/ijo.2014.2615 | 2014 |
Pterocarpanquinone LQB-118 Induces Apoptosis in Leishmania (Viannia) braziliensis and Controls Lesions in Infected Hamsters | 10.1371/journal.pone.0109672 | 2014 |
Theoretical and Experimental Studies of New Modified Isoflavonoids as Potential Inhibitors of Topoisomerase I from Plasmodium falciparum | 10.1371/journal.pone.0091191 | 2014 |
The pterocarpanquinone LQB-118 inhibits tumor cell proliferation by downregulation of c-Myc and cyclins D1 and B1 mRNA and upregulation of p21 cell cycle inhibitor expression | 10.1016/j.bmc.2014.04.025 | 2014 |
The pterocarpanquinone LQB 118 induces apoptosis in tumor cells through the intrinsic pathway and the endoplasmic reticulum stress pathway | 10.1097/cad.0b013e3283592da8 | 2013 |
Evaluation of Coumarin and Neoflavone Derivatives as HCV NS5B Polymerase Inhibitors | 10.1111/cbdd.12105 | 2013 |
Palladium-Catalyzed Arylation of Enoates with Iodobenzene: Stereoselective Synthesis of Trisubstituted Olefins | 10.5935/0103-5053.20130067 | 2013 |
The Therapeutical Potential of a Novel Pterocarpanquinone LQB-118 to Target Inhibitor of Apoptosis Proteins in Acute Myeloid Leukemia Cells | 10.2174/1871520611313020019 | 2013 |
LQB-118, an orally active pterocarpanquinone, induces selective oxidative stress and apoptosis in Leishmania amazonensis | 10.1093/jac/dks498 | 2013 |
Purification of a synthetic pterocarpanquinone by countercurrent chromatography | 10.1590/s0103-50532012000600016 | 2012 |
A new type of pterocarpanquinone that affects Toxoplasma gondii tachyzoites in vitro | 10.1016/j.vetpar.2011.11.008 | 2012 |
Binap-silver salts as chiral catalysts for the enantioselective 1,3-dipolar cycloaddition of azomethine ylides and alkenes | 10.1016/j.tetasy.2012.10.015 | 2012 |
214. Evaluation of the Antiophidic Activity of Lapachol and Synthetic Analogues | 10.1016/j.toxicon.2012.04.215 | 2012 |
Microwave-Promoted Palladium-Catalysed Oxyarylation of Dihydronaphthalene and Chromenes by o-Iodophenols and Its Acetates | 10.1002/ejoc.201100365 | 2011 |
LQB-118, a pterocarpanquinone structurally related to lapachol [2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone]: a novel class of agent with high apoptotic effect in chronic myeloid leukemia cells | 10.1007/s10637-010-9453-z | 2011 |
Effectiveness of the local or oral delivery of the novel naphthopterocarpanquinone LQB-118 against cutaneous leishmaniasis | 10.1093/jac/dkr158 | 2011 |
DBU as a catalyst for the synthesis of amides via aminolysis of methyl esters | 10.1590/s0103-50532011001100023 | 2011 |
Synthesis of Coumarins and Neoflavones through Zinc Chloride Catalyzed Hydroarylation of Acetylenic Esters with Phenols | 10.1055/s-0031-1289576 | 2011 |
Pterocarpanquinones, Aza-pterocarpanquinone and Derivatives: Synthesis, Antineoplasic Activity on Human Malignant Cell Lines and Antileishmanial Activity on Leishmania amazonensis | 10.1016/j.bmc.2011.09.025 | 2011 |
1213 POSTER The New Synthetic Compound Pterocarpanquinone LQB-118 Induces Apoptosis in Acute Myeloid Leukemia Cells Through Survivin and XIAP Downregulation | 10.1016/S0959-8049(11)70825-5 | 2011 |
A new and concise strategy to the enantioselective synthesis of (S)-2-amino-4-oxo-4-(pyridine-2-yl) butanoic acid from aspartic acid | 10.1590/s0103-50532010000500002 | 2010 |
BINAP-AgSbF6 vs. BINAP-AgClO4 Complexes as Catalysts for the Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides and Alkenes | 10.1055/s-0029-1219534 | 2010 |
Ability of a synthetic coumestan to antagonize Bothrops snake venom activities | 10.1016/j.toxicon.2009.09.021 | 2010 |
Palladium-catalyzed oxyarylation of olefins using silver carbonate as the base. Probing the mechanism by electrospray ionization mass spectrometry | 10.1016/j.jorganchem.2010.05.014 | 2010 |
New pterocarpanquinones: Synthesis, antineoplasic activity on cultured human malignant cell lines and TNF-α modulation in human PBMC cells | 10.1016/j.bmc.2009.12.073 | 2010 |
Palladium-Catalyzed Tandem Heck-Lactonization from o -Iodophenols and Enoates: Synthesis of Coumarins and the Study of the Mechanism by Electrospray Ionization Mass Spectrometry | 10.1021/jo1010922 | 2010 |
Comparison of the cytotoxic effect of lapachol, α-lapachone and pentacyclic 1,4-naphthoquinones on human leukemic cells | 10.1007/s10637-009-9231-y | 2010 |
Antitumoral, Antileishmanial and Antimalarial Activity of Pentacyclic 1,4-Naphthoquinone Derivatives | 10.1590/S0103-50532009000100026 | 2009 |
(±)-3,4-Dihydroxy-8,9-methylenedioxypterocarpan and derivatives: Cytotoxic effect on human leukemia cell lines | 10.1016/j.ejmech.2008.01.027 | 2009 |
N-tert-Butyl and N-Methyl Nitrones Derived from Aromatic Aldehydes Inhibit Macromolecular Permeability Increase Induced by Ischemia/Reperfusion in Hamsters | 10.1016/j.bmc.2009.04.004 | 2009 |
Inhibition of the a1b1 Isoform of the Na, K-ATPase by 8-Methoxycoumestrol without Positive Inotropic Effect in Human Myocardium - Novel Aspects of Cardiac Glycoside Pharmacology | 10.1097/FJC.0b013e3181a95ab2 | 2009 |
Iodination of Phenols in Water Using Easy to Hanle Amine-Iodine Complexes | 10.1590/s0103-50532009001000021 | 2009 |
Synthesis of 5-Deoxypterocarpens,Pterocarpens and Coumestans by Intramolecular Heck Reaction. | 10.1016/j.tetlet.2009.01.004 | 2009 |
Natural products as starting point for the discovery of new bioactive compounds: Drug candidates with antiophidic, anticancer and antiparasitic properties | 10.5935/1984-6835.20090008 | 2009 |
Identification and characterization of coumestans as novel HCV NS5B polymerase inhibitors | 10.1093/nar/gkm1178 | 2008 |
First stereoselective synthesis and assignment of the absolute configuration of the nebracetam eutomer and derivatives | 10.1016/j.tetasy.2008.04.012 | 2008 |
Reação entre Nitrofenilmetanos e Enoato Derivado do D-manitol na Presença de TBAF ou DBU. Adição Conjugada Sin-Seletiva e Reação de Nef Consecutiva. | 10.1590/S0100-40422008000400024 | 2008 |
Insights into the mechanism of Na+,K+-ATPase inhibition by 2-methoxy-3,8,9-trihydroxy coumestan | 10.1016/j.bmc.2008.09.007 | 2008 |
A tandem palladium-catalyzed Heck-lactonizationthrough the reaction of ortho-iodophenols with beta-substituted acrylates: synthesis of 4,6-substituted coumarins. | 10.1016/j.tetlet.2008.03.037 | 2008 |
Synergistic interaction between ouabain and 8-methoxy-3,9-dihydroxy coumestan, a non-steroidal synthetic inhibitor of Na+,K+-ATPase | 10.1016/j.lfs.2007.08.021 | 2007 |
Alfa-Phenyl-N-ter-butyl nitrone (PBN) derivatives:Synthesis and protective action against microvascular damages induced by ischemia/reperfusion | 10.1016/j.bmc.2007.02.033 | 2007 |
Configuration assignment of stereogenic centers in a beta-pinene derivative by 1H NMR and molecular modeling. | 10.1016/j.molstruc.2005.09.001 | 2006 |
Structure- activity relationship of wedelolactone analogues: Structural requirements for inhibition of Na+,K+-ATPase and binding to the central benzodiazepine receptor. | 10.1016/j.bmc.2006.07.053 | 2006 |
Synthesis and pharmacological evaluation of prenylated and benzylated pterocarpans against snake venom | 10.1016/j.bmcl.2003.10.044 | 2004 |
The First Synthesis of (+/-)-3,4-dihydroxy-8,9-methylenedioxypterocarpan, an Antitumoral Agente and its Cumestan Derivative | 10.1590/S0103-50532004000600029 | 2004 |
Stereoselective preparation of pyrrolidin-2-ones from a Z-enoate derived from -(+)-mannitol | 10.1016/j.tetasy.2004.06.013 | 2004 |
Stereoselective synthesis and preliminary evaluation of new d-3-heteroarylcarbonylalanines as ligands of the NMDA receptor | 10.1016/j.bmcl.2004.06.062 | 2004 |
Characterization of a new synthetic isoflavonoid with inverse agonist activity at the central benzodiazepine receptor | 10.1016/j.ejphar.2004.05.026 | 2004 |
Crude D-( )-Glyceraldehyde Obtained from D-mannitol-diacetonide by Oxidative Cleavage with Sodium Periodate :Its Reactions with Nucleophilic Species. | 10.1081/SCC-120027706 | 2004 |
Stereoselective conjugate addition of benzyl phenylsulfonyl carbanions to enoates derived from D-mannitol | 10.1021/jo035427d | 2004 |
Highly Stereocontrolled Synthesis of Natural Barbacenic Acid, Novel Bisnorditerpene From Barbacenia flava | 10.1021/jo0340049 | 2003 |
2-Methoxy-3,8,9-trihydroxy coumestan: a new synthetic inhibitor of Na+,K+-ATPase with an original mechanism of action | 10.1016/j.bcp.2003.08.005 | 2003 |
Stereoselective Mannich Reaction of Camphor Titanium Enolate | 10.1016/S0957-4166(02)00260-4 | 2002 |
Selective Conjugate Addition of Nitromethane to Enoates Derived from D-Mannitol and L-tartaric acid | 10.1016/S0957-4166(02)00230-6 | 2002 |
Synthesis and Preliminary Pharmacological Evaluation of new (+/-) 1,4-Naphthoquinones Structurally Related to Lapachol | 10.1016/S0968-0896(02)00100-1 | 2002 |
NaBH4-MnCll2 for Improved Reduction of Beta-keto Esters Attached to a Chiral Auxiliary. Comparison with Zn(BH4)(2) | 10.1080/00304940209355768 | 2002 |
4-Chromenesulphones: Synthesis and Transformation to Isoflavonoid Models | 10.1016/S0040-4039(02)01653-2 | 2002 |
25 anos de Reações, Estratégias e Metodologias em Química Orgânica | 10.1590/S0100-40422002000800012 | 2002 |
The 1,4-addition of organometallic reagents to enoates derived from pinanediol | 10.1016/s0957-4166(02)00688-2 | 2002 |
The reaction of safrole derivatives with aluminum chloride improved procedures for preparation of catechols or their mono-o-methylated derivatives and a mechanistic interpretation. | 10.1590/S0103-50532001000300005 | 2001 |
Synthesis and Preliminary Pharmacological Evaluation of Coumestans with Different Patterns of Oxygenation | 10.1016/S0960-894X(00)00621-1 | 2001 |
Synthesis of beta -Amino Arylketones Through the Addition of ArLi Derivatives to beta-Aminoester | 10.1016/S0040-4039(01)00358-6 | 2001 |
A Practical and Efficient Preparation of (-)-(4aS,5R)-4,4a,5,6,7,8-hexahydro-4a,5-dimethyl- 2(3H)-naphthalenone: A Key Intermediate in the Synthesis of (-)-Dehydrofukinone, | 10.1016/S0957-4166(01)00089-1 | 2001 |
Regioselective lithiations of a Pterocarpan Skeleton: The First Synthesis of (+/-)-4 '-Dehydroxycabenegrin A-I | 10.1016/S0040-4039(01)00682-7 | 2001 |
Safrol e Eugenol: Estudo da ReatividadeQuímica e uso em Síntese de Produtos Naturais Biológicamente ativos e seus Derivados | 10.1590/S0100-40422000000300013 | 2000 |
The use of Chiral Auxiliaries Prepared From (-)- Beta - Pinene in stereoselective Reduction of Beta -Ketobutyrates | 10.1080/00397910008087342 | 2000 |
Synthesis of Chiral Pyrrolidine and Pyrrole Derivatives Through the Chemoselective Dieckmann | 10.1016/S0957-4166(00)00377-3 | 2000 |
The Regio- and Stereoselective Oxyamination of Pinenes and Camphene | 10.1016/S0957-4166(00)00382-7 | 2000 |
Synthesis of new chiral auxiliares from carbohydrates for Et2AlCl-promoted Diels-Alder Reactions | 10.1590/S0103-50532000000300012 | 2000 |
Formal Enantioselective Synthesis of (+)-Vincamine. The First Enantioselective Route to (+)-3,14-Epivincamine and Its Enantiomer, | 10.1016/S0957-4166(98)00489-3 | 1999 |
Improved Method for the Esterification of Sugar Acetals With Dicyclocarbodiimide | 10.1080/00304949909355350 | 1999 |
Syn or Anti Selective Michael Addition of Allyl Phenyl Sulphone and Phenyl Prenyl Sulphone to Enoates Derived From D-Mannitol, | 10.1016/S0040-4039(98)01073-9 | 1998 |
New Carbohydrate-Based Chiral Auxiliaries in Diels-Alder Reaction | 10.1016/S0957-4166(98)00286-9 | 1998 |
Carboxyl-Terminal Sequencing: New C-Terminal Peptidyl-ThioHydantoins Formation Conditions | 1998 | |
Synthesis and structural determination of new chiral auxiliaries derived from (-)-b-pinene | 10.1016/S0957-4166(96)00523-X | 1997 |
Stereocontrolled Elaboration of Quaternary Carbon Centers Involving the Asymmetric Michael-type Alkylation of Chiral Imines: an Efficient Enantioselective Access to (+)-Vincamine | 10.1016/S0957-4166(97)00210-3 | 1997 |
Syn-selective Michael Addition of nitromethane derivatives to enoates derived from (R)-(+)-glyceraldehyde acetonide | 10.1021/jo960788x | 1997 |
Substâncias Enantiomericamente Puras (SEP): A questão dos fármacos quirais | 10.1590/S0100-40421997000600014 | 1997 |
Asymmetric Friedel-Crafts Reactio Mediated by New Chiral Auxiliaries Derived From (1S)-(-)-(b)-Pinene: Enantioselective Synthesis of (-)-8-Norethyl, 1'-Normethyl Etodolac | 10.1016/S0040-4039(97)01658-4 | 1997 |
One Pot Large Scale Procedure for the Production of 2-Ethyl and 2-Butyl-2-Carboethoxycyclopentanone frm Ethyl Adipate, | 10.1080/00397919708005062 | 1997 |
Carbohydrates and Terpenes as Chiral Auxiliaries: the Stereoselective Synthesis of (+) or (-)-b-Piperonyl-g-butirolactone | 1996 | |
2,3;4,5-Bis-O-(1-methylethyledene)-b-D-fructopiranose as chiral auxiliary in asymmetric a-alkylation of ester enolates | 10.1080/07328309608005685 | 1996 |
Asymmetric Friedel - Crafts Reaction: An Application to the Synthesis of an Etodolac Analogue | 10.1080/00397919608003781 | 1996 |
Orthobromodiphenylmethane derivatives as starting material for the total synthesis of anthraquinones | 10.1080/00397919608003853 | 1996 |
Snthesis of (-)-6,6-(ethylenedioxy)-1,10-dimethyl-1(9)-octal-2-one | 1996 | |
Variable Chemo-selective Electrophilic Attack on Silylated Aromatic Aldehydes | 10.1055/s-1996-5530 | 1996 |
Total synthesis of pterocarpan: (?)-neorautenane | 10.1039/P19950000949 | 1995 |
Stereoselective conjugate addition of Nitromethane to enolates derived from Glyceraldehyde acetonide | 1994 | |
Stereoselectivity of enolate formations: the effect of the substituent in the g-position of butirates | 1994 | |
Enantioselective synthesis of (R)-(+)-b-piperonil-Y-butirolactone | 10.1016/0957-4166(94)80161-4 | 1994 |
Enantioselective synthesis of substituted octalones | 10.1016/0957-4166(94)80104-5 | 1994 |
On the asymmetric induction involving lithium enolates of l-menthylpropionate | 10.1016/S0957-4166(00)86253-9 | 1994 |
On the enantioselective formal synthesis of (+)-Vallesamidine, an Aspidospermae alkaloid, | 1993 | |
A convenient synthesis of (±)-4-prenylpterocarpin, | 1992 | |
Trans-2-arylcyclohexanols: use as auxiliaries in the Mukaiyama aldol-type condensation between silyl enol esters and aldehydes | 10.1016/S0040-4039(00)61234-0 | 1992 |
Piperonal as starting material for the regioespecific and stereoselective synthesis of E and Z isomers of 3-methyl-2-hexenedioic acid-1-methyl ester, | 10.1080/00397919108020839 | 1991 |
Synthesis of 6,7-methylenedioxylapachol | 10.1080/00397919108020840 | 1991 |
Asymmetric Michael addition of chiral imines to phenylvinylsulphone: Preparation of key chiral building blocks for the synthesis of Aspidosperma and Hunteria alkaloids | 10.1016/S0957-4166(00)82358-7 | 1991 |
New chiral auxiliaries derived from beta-pinene: their use in the asymmetric reduction of b-keto-esters | 1991 | |
Safrole as starting material for the synthesis of 7-methoxy-3'-4'-methylenedioxy isoflavone | 1990 | |
Vanillin (1) as starting material for the synthesis of isomeric phthalides | 10.1080/00397918808081335 | 1988 |
Synthesis of Dimethoxyfuronaphthoquinones | 10.1080/00397918808081336 | 1988 |
Expeditious, stereocontrolled synthesis of racemic and natural brasilenol through intramolecular symetry transfer. Absolute stereochemistry of brasilenol | 10.1021/jo00382a042 | 1987 |
The synthesis of new hybrid prostanoids from natural safrole | 1987 | |
Eugenol as starting materials for the synthesis of 3-alkyl muconic acid dimethyl esteres and 3-alkyl adipic acid dimethyl ester | 1986 | |
Safrole as starting materials for the synthesis of 3-alkyl muconic acid monomethyl esters an 4,4-dialkylbutenolides | 1986 | |
The chemistry of phthalides. I. Synthesis of 2,3-dimethoxy-phthalide (Meconime) and 2-benzyloxyphthalide, | 1986 | |
A selective synthesis of brasilenol, a novel sesquiterpene from the sea hare Aplysia brasiliana and the red alga Laurencia obtusa | 10.1021/jo00372a027 | 1986 |
Prostaglandin analogue: 2. The synthesis of new prostanoids derivatives from safrole isolated from sassafraz oil | 1985 | |
Eugenol and Safrole as starting materials for the synthesis of 3-alkyl-muconic acids mono and dimethyl ester and 4,4-dialkylbutenolids | 10.1016/S0040-4039(00)98978-0 | 1985 |
The reaction of safrole with brominating agents. Differential trapping of the intermediates by bromide and water | 1984 | |
The nature of solvent effects in the reaction of safrole with bromine | 1984 | |
Efficient synthesis of cytotoxic quinones; 2-acetyl-4H,9H-naphtho [2,3-b] furan-4,9-dione, 6 and (+) 2-(1-hydroxy-ethyl)-4H,9H-naphtho [2,3-b] furan-4,9-dione, 7 | 10.1002/jhet.5570210274 | 1984 |
Prostaglandin analogues: The synthesis of new prostaglandins from natural safrole | 1984 | |
Prostaglandin analogues: the synthesis of new tromboxaxane derivatives from natural safrole | 1984 | |
Interaction of a nitro-group with adjacent cationic species to form nitronic lactones | 1983 | |
Eergia da ponte de hidrogênio entre moléculas S-trans na N-metil-formamida: cálculos pelo método CNDO/ | 1983 | |
A convenient method for the preparation of 6,7-methylenedio-xy-3-alkyl-2-hydroxy-1,4-naphthoquinones from natural safrole and carboxylic acids | 10.1080/00397918308060351 | 1983 |
The Bayer-Villiger reactions in the synthesis of vicinal triphenol derivatives, | 1982 | |
An improved synthesis from natural safrole of indole related to indomethacin | 1982 | |
Preparação de aldeídos fenilacéticos oxigenados pela reação de ozonólise de alilbenzenos naturais - Utilização do homopiperonal como precursor de unidades C6-C2 | 1982 | |
Síntese de derivados do ácido 2,3-indoil-acético a partir do safrol | 1982 | |
Síntese do 2-acetil-4H,9H-nafto[2,3-b]furan-4,9-diona e (+) 2-(1-hidroximetil)-H,9H-nafto[2,3-b]furan-4,9-diona | 1982 | |
Utilização de sintons naturais na preparação de compostos biologicamente ativos. I. Prostanóides | 1981 | |
Utilização de sintons naturais na preparação de compostos biologicamente ativos. II. Antiinflamatórios | 1981 | |
Reações de Bayer-Villiger: aplicação na síntese de trifenóis vicinais e O-derivados | 1981 | |
Síntese de quinolinas a partir do safrol | 1980 | |
Ions carbônio não clássicos em reações de adição eletrofílica ao safrol | 1975 | |
Solvent Effects in the Reaction of Safrole with Bromine | 10.1016/S0040-4039(00)91064-5 | 1975 |
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