Photoacidity as a tool to rationalize excited state intramolecular proton transfer reactivity in flavonols-Reference-Cited by-同舟云学术

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Photoacidity as a tool to rationalize excited state intramolecular proton transfer reactivity in flavonols

Published:2018 Issue:2 Volume:17 Page:231-238
ISSN:1474-905X
Container-title:Photochemical & Photobiological Sciences
language:en
Short-container-title:Photochem. Photobiol. Sci.

Author:

Duarte Luís Gustavo Teixeira Alves¹²³⁴⁵^ORCID,Germino José Carlos⁶⁷⁸⁵^ORCID,Braga Cláudia de Ávila¹²³⁴⁵^ORCID,Barboza Cristina Aparecida⁹¹⁰¹¹¹²^ORCID,Atvars Teresa Dib Zambon⁶⁷⁸⁵,Santos Fabiano da Silveira¹²³⁴⁵^ORCID,Rodembusch Fabiano Severo¹²³⁴⁵^ORCID

Affiliation:

1. Grupo de Pesquisa em Fotoquímica Orgânica Aplicada

2. Universidade Federal do Rio Grande do Sul

3. Instituto de Química

4. Porto Alegre

5. Brazil

6. Chemistry Institute

7. University of Campinas

8. Campinas

9. Institute of Physics

10. Polish Academy of Sciences

11. Warsaw

12. Poland

Abstract

Determination of acidic strengths at the electronic ground and excited states of flavonol derivatives.

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/PP/C7PP00334J

Reference69 articles.

1. Total Synthesis of Hapalindole-Type Natural Products

2. Effect of acetylation on the properties of microfibrillated cellulose-LDPE composites

3. Copper-Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis

4. Natural Products as Sources of New Drugs over the Last 25 Years

5. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

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