Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones (2013)
- Authors:
- Autor USP: EMERY, FLAVIO DA SILVA - FCFRP
- Unidade: FCFRP
- DOI: 10.1016/j.ejmech.2013.07.057
- Subjects: DOENÇA DE CHAGAS; LEISHMANIA
- Language: Inglês
- Imprenta:
- Publisher place: Issy les Moulineaux
- Date published: 2013
- Source:
- Título: European Journal of Medicinal Chemistry
- ISSN: 0223-5234
- Volume/Número/Paginação/Ano: v. 69, p. 678-700, 2013
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
CASTRO, Solange L. de e EMERY, Flavio da Silva e SILVA JÚNIOR, Eufrânio N. da. Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones. European Journal of Medicinal Chemistry, v. 69, p. 678-700, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2013.07.057. Acesso em: 14 fev. 2026. -
APA
Castro, S. L. de, Emery, F. da S., & Silva Júnior, E. N. da. (2013). Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones. European Journal of Medicinal Chemistry, 69, 678-700. doi:10.1016/j.ejmech.2013.07.057 -
NLM
Castro SL de, Emery F da S, Silva Júnior EN da. Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones [Internet]. European Journal of Medicinal Chemistry. 2013 ; 69 678-700.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2013.07.057 -
Vancouver
Castro SL de, Emery F da S, Silva Júnior EN da. Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones [Internet]. European Journal of Medicinal Chemistry. 2013 ; 69 678-700.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2013.07.057 - A review of the synthetic strategies for the development of BODIPY dyes for conjugation with proteins
- On the search for potential anti-Trypanosoma cruzi drugs: synthesis and biological evaluation of 2-hydroxy-3-methylamino and 1,2,3-triazolic naphthoquinoidal compounds obtained by clik chemistry reactions
- On the synthesis of quinone-based BODIPY hybrids: New insights on antitumor activity and mechanism of action in cancer cells
- Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes
- Naftotiazóis inibidores de dihidroorotato desidrogenase potenciais agentes leishmanicidas
- Síntese de análogos heterocíclicos do aripiprazol
- Oral administration of peptide-based drugs: beyond Lipinski's rule
- Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives
- Claisen rearrangement of hydroxynaphthoquinones: selectivity toward naphthofuran or α-xiloidone using copper salts and iodine
- Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine
Informações sobre o DOI: 10.1016/j.ejmech.2013.07.057 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas