Setembro 2013 vol. 1 num. 1 - Brazilian Meeting on Organic Synthesis 2011
Abstract - Open Access.
A New Method to Prepare 3-Alkyl-2-hydroxy-1,4- naphthoquinones. Synthesis of Lapachol and Phthiocol.
Rocha, David R. da ; Ferreira, Sabrina B. ; Carneiro, José Walkimar M. ; Santos, Wilson C. ; Ferreira, Vitor F. ;
Abstract:
Alkyl-1,4-naphthoquinones constitute an important group of compounds that present some types of biological activity. 3-Substituted-2-hydroxy-1,4- naphthoquinones such as lapachol (1) exhibit a broad spectrum of activities. Lapachol (1) is also widely used by the scientific community as a raw material for the synthesis of various bioactive derivatives and analogues, with _-lapachone (2) being one of the main lapachol derivatives. For this reason, the isolation, structure elucidation and synthesis of 2-hydroxy-3-alkyl-1,4- naphthoquinones, especially lapachol, has attracted a lot of attention.
Abstract:
Palavras-chave: Quinones, Alkylation, Lapachol synthesis,
Palavras-chave: ,
DOI: 10.5151/chempro-14bmos-R0061-1
Referências bibliográficas
- [1] 1 Santos, A. F.; Ferraz, P. A. L.; Pinto, A. V.; Pinto, M. C. F. R.; Goulart, M. O. F.; Sant'Ana, A. E. G. Int. J. Parasitol. 2000, 30, 1199.
 
- [2] 2 Hussain, H.; Krohn, K.; Ahmad, V. U.; Miana, G. A.; Greend, I. R. Arkivoc 2007, Part II, 145.
 
Como citar:
                                                                    Rocha, David R. da;                                     Ferreira, Sabrina B.;                                     Carneiro, José Walkimar M.;                                     Santos, Wilson C.;                                     Ferreira, Vitor F.;                                 "A New Method to Prepare 3-Alkyl-2-hydroxy-1,4- naphthoquinones. Synthesis of Lapachol and Phthiocol.",                                     p. 61                                                                . In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013.
                                                                    São Paulo: Blucher,
                                
                                2013. 
                                ISSN 2318-4043,
                                
                                
                                                                            DOI 10.5151/chempro-14bmos-R0061-1                                                                                                
últimos 30 dias | último ano | desde a publicação
downloads
visualizações
indexações
