53. 2019: Seminário no Departamento de Química da Universidade Federal de Minas Gerais (UFMG), Brasil.

Exploring different facets of catalysis towards bioactive quinoidal compounds: The complexity of simple and powerful molecules.

52. 2019: The Brazilian Symposium on Medicinal Chemistry (BrazMedChem), Pirenopolis, Goiás, Brazil.

Exploring different facets of catalysis towards bioactive quinoidal compounds: The complexity of simple and powerful molecules.

51. 2019: Annual Göttinger Chemistry Forum, Göttingen, Germany.

Exploring different facets of catalysis and quinoidal systems: A new frontier for potent trypanocidal quinones.

50. 2019: 14th International Conference on the Chemistry of Selenium and Tellurium (ICCST-14), Sardinia, Italy.

Strategies towards bioactive quinoidal molecules: Synthesis and antitumor activity of selenium-containing quinones.

49. 2019: University of Bristol, Bristol, UK.

Exploring different facets of catalysis and quinoidal systems: A new frontier for potent trypanocidal quinones.

48. 2019: National University of Ireland Galway, Galway, Ireland.

Exploring different facets of catalysis and quinoidal systems: A new frontier for potent trypanocidal quinones.

 

47. 2019: UCD School of Chemistry - University College Dublin, Dublin, Ireland.

Exploring different facets of catalysis and quinoidal systems: A new frontier for potent trypanocidal quinones.

46. 2018: CiQUS - Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares, Santiago de Compostela, Spain.

Metal-catalyzed C‒H Bond Activation and Oxidation Reactions towards Quinoidal Systems: The Special Case of A-ring Functionalization.

45. 2018: Nicolaus Copernicus University, Torun, Poland.

Metal-catalyzed C‒H Bond Activation and Oxidation Reactions towards Quinoidal Systems: The Special Case of A-ring Functionalization.

44. 2018: Centre of Molecular and Macromolecular Studies, Lodz, Poland.

Metal-catalyzed C‒H Bond Activation and Oxidation Reactions towards Quinoidal Systems: The Special Case of A-ring Functionalization.

43. 2018: Network Meeting of the Alexander von Humboldt Foundation - Rheinische Friedrich-Wilhelms-Universität Bonn, Germany.

On the Synthesis of Bioactive Quinoidal Molecules via C-H Functionalization Logic: A new frontier for potent trypanocidal quinones.

42. 2018: The University of Warwick, Warwick, United Kingdom.

Metal-catalyzed C‒H Bond Activation and Oxidation Reactions towards Quinoidal Systems: The Special Case of A-ring Functionalization.

41. 2018: Universität Göttingen - Georg-August-Universität Göttingen, Gottingen, Germany.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

40. 2018: 6th Brazil-Spain Workshop in Organic Chemistry - Oviedo, Spain.

Metal-catalyzed C‒H Bond Activation and Oxidation Reactions towards Quinoidal Systems: The Special Case of A-ring Functionalization

39. 2018: 22st International Conference on Organic Synthesis - ICOS 22, Italy.

Direct sequential C-H iodination/organoyl-thiolation for quinoidal deactivated systems: A new protocol for potent trypanocidal quinones.

38. 2018: Saarland University - Saarbrücken, Germany.

On the synthesis of bioactive quinoidal molecules via C-H functionalization logic. A new frontier for potent trypanocidal quinones.

37. 2018: Commissariat à l'Énergie Atomique et aux Énergies Alternatives (CEA-Saclay), Saclay, France.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

36. 2018: Université de Lorraine, Metz, France.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

35. 2018: Sessão Coordenada de Química Orgânica II, 41º Reunião anual da SBQ, Brazil.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

34. 2017: II Workshop do Programa de Pós-Graduação em Química da UFG, Goiânia, Brazil.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

33. 2017: Institute of Pharmaceutical and Medicinal Chemistry - Westfälische Wilhelms - Universität Münster - Münster, Germany.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

32. 2017: 6th Workshop of SeS Redox and Catalysis (WSeS-6) - Wrocław, Poland.

Strategies towards Bioactive Quinoidal Molecules: Synthesis and antitumor activity of Selenium- and Sulfur-containing Quinones.

31. 2017: Saarland University - Saarbrücken, Germany.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

30. 2017: Leibniz Institute of Plant Biochemistry - Halle, Germany.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

29. 2017: Biomedical Research Center, Slovak Academy of Sciences, Slovakia.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges in Quinone-Based Chemistry.

28. 2017: Programa de Pós-Graduação em Química - Universidade Federal do Ceará, Brazil.

Overcoming Challenges in Quinone-Based Chemistry.

27. 2017: Programa de Pós-Graduação em Química - Universidade Federal de Santa Catarina, Brazil.

Overcoming Challenges in Quinone-Based Chemistry.

26. 2017: Programa de Pós-Graduação em Química - Universidade Federal do Mato Grosso do Sul, Brazil.

Overcoming Challenges in Quinone-Based Chemistry.

25. 2017: Programa de Pós-Graduação em Química - Universidade Federal de Grande Dourados, Brazil.

Overcoming Challenges in Quinone-Based Chemistry.

24. 2016: School of Pharmacy, Saarland University, Germany.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges by using Rhodium-catalyzed C-H activation, Click and Asymmetric Reactions.

23. 2016: Frank Warren Conference, South Africa.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges by using Rhodium-catalyzed C-H activation, Click and Asymmetric Reactions.

22. 2016: 21st International Conference on Organic Synthesis - ICOS 21, India.

Rhodium-Catalyzed Reactions of 1,4-Benzoquinones with Electrophiles.


21. 2016: Institute of Chemistry, Indian Institute of Technology Bombay, IIT Bombay, India.

Overcoming Naphthoquinone Deactivation for the Synthesis of Quinoidal Molecules by Transition Metal-Catalyzed Reactions: Strategies towards Bioactive Compounds.

20. 2016: Programa de Pós-Graduação em Química - Universidade Estadual de Campinas, Brazil.

Strategies towards Bioactive Quinoidal Molecules: Overcoming Challenges by using Rhodium-catalyzed C-H activation, Click and Asymmetric Reactions.


19. 2016: 39º Reunião da SBQ - Italo-Brazilian Symposium on Organic Chemistry, Brazil.

Synthesis of Quinoidal Molecules by using Organocatalysis and Transition Metal-Catalyzed Reactions: Strategies towards Bioactive Compounds.


18. 2016: VI ESeTe - Encontro sobre Selênio e Telúrio, Brazil.

Estratégias para Modificações Estruturais em Protótipos Naftoquinoidais: Síntese e atividade antitumoral de Quinonas contendo Selênio e Enxofre.


17. 2016Programa de Pós-Graduação em Ciências Farmacêuticas - Universidade Federal de São João del Rei, Brazil. 

Synthesis of Quinoidal Molecules by using Organocatalysis and Transition Metal Catalyzed Reactions: Strategies towards Bioactive Compounds.

16. 2015: Sessão Coordenada de Química Medicinal da 38º Reunião da Sociedade Brasileira de Química, Brazil.

Um método rápido, verde e eficiente para a obtenção de naftoquinonas contendo calcogênios: Potente atividade antitumoral e estudos de mecanismos de ação.

15. 2015: The 25th International Society of Heterocyclic Chemistry Congress, California, United States of America.

Structural Modifications of Quinoidal Molecules towards Bioactive and Fluorescent Heterocycles.

14. 2015: Department of Pharmacy and Biotechnology (FaBit), Alma Mater Studiorum, University of Bologna, Italy.

Synthesis of Quinoidal Molecules: Strategies towards Potent Antitumor Compounds and Fluorescent Probes.

13. 2015: 10th International Congress of Pharmaceutical Sciences, Ribeirão Preto (SP), Brazil.

Strategies for Chemical Synthesis of Antitumor Molecules inspired by Redox Centre and Ring Modifications.

12. 2015: Programa de Pós-Graduação em Química - Universidade Federal de São Carlos, Brazil.

Strategies for Chemical Synthesis of Bioactive Quinoidal Molecules and Related Compounds inspired by Redox Centre and Ring Modifications.

11. 2015: Programa de Pós-Graduação em Química - Universidade Federal do Rio Grande do Sul, Brazil.

Synthesis of Hybrid Quinoidal Compounds as Promising Antitumor Agents.

10. 2015: 16th BMOS - Brazilian Meeting on Organic Synthesis, Brazil.

Strategies for Chemical Synthesis of Bioactive Quinoidal Molecules and Related Compounds inspired by Redox Centre and Ring Modifications.

9. 2014: Sessão Coordenada de Química Orgânica da 37º Reunião da Sociedade Brasileira de Química, Brazil.

Estratégias para Modificações Estruturais em Protótipos Naftoquinoidais: Síntese, Avaliação do Potencial Biológico e Estudos de Localização Subcelular.

8. 2013: Programa de Pós-Graduação em Química - Universidade Federal de Santa Maria, Brazil.

Estratégias para Modificações Estruturais em Protótipos Bioativos, Marcadores e Sondas Luminescentes.

7. 2013: Programa de Pós-Graduação em Química - Universidade Federal de Santa Catarina, Brazil.

Estruturas Naftoquinoidais e Heterocíclicas Versáteis: Síntese de Moléculas Bioativas, Marcadores e Sondas Luminescentes.

6. 2012: Programa de Pós-Graduação em Ciências Farmacêuticas - Universidade de São Paulo, Brazil.

Heterocíclicos Quinoidais Privilegiados: Estratégias Sintéticas para a obtenção de Substâncias relacionadas à Quimioterapia de Doenças Negligenciadas.

5. 2011: Programa de Pós-Graduação em Química da UFMG, Brazil.

Síntese de substâncias naftoquinoidais e heterocíclicas voltadas à obtenção de protótipos com potente bioatividade.

4. 2010: Programa de Pós-Graduação em Física e Química Aplicadas, UFSJ, Brazil.

Reatividade Química de Produtos Naturais voltados à Obtenção de Protótipos Quinoidais Bioativos.

3. 2008: Programa de Educação Tutorial do Instituto de Química da Universidade de Brasília, Brazil.

Heterocíclicos Bioativos: 'Click Reactions' para a obtenção de compostos nitrogenados.

2. 2008: Programa de Educação Tutorial do Instituto de Química da Universidade de Brasília, Brazil.

Nor-lapachonas substituídas em C-3: potente atividade tripanocida e antitumoral.

1. 2007: Seminários de Graduação em Química, Universidade de Brasília, Brazil.

Quinonas-protótipo para a doença de Chagas e o Câncer: síntese de lapachonas e nor-lapachonas ativas

Laboratory of Synthetic and Heterocyclic Chemistry,

Institute of Exact Sciences, Department of Chemistry,
Federal University of Minas Gerais, Belo Horizonte, Brazil

Adress : Av. Pres. Antônio Carlos, 6627 - Pampulha,

Belo Horizonte - MG

E-mail: eufranio@ufmg.br

Phone Number: +55 31 34095696