'A POT. 3'-coupling reaction as a strategy towards the synthesis of alkaloids (2015)
- Authors:
- USP affiliated authors: COMASSETO, JOAO VALDIR - IQ ; SANTOS, ALCINDO APARECIDO DOS - IQ
- Unidade: IQ
- Subjects: ALCALOIDES; ALDEÍDOS; SÍNTESE ORGÂNICA
- Language: Inglês
- Abstract: Uma série de aldeídos, alquinóis e benzilaminas foram submetidos a reação, por catálise mediada por CuCl, na formação de hidróxi-benzilaminas funcionalizadas. O procedimento permite a utilização de aldeídos alquílicos e arílicos. Substratos representativos foram convertidos em alcalóides cíclicos de cinco e seis membros através da reação concomitante de N-debenzilação e redução total da ligação tripla promovida por Pd, seguido de ciclização tipo Mitsunobu
- Imprenta:
- Source:
- Título: Journal of the Brazilian Chemical Society
- ISSN: 0103-5053
- Volume/Número/Paginação/Ano: v. 26, n. 1, p. 117-123, 2015
-
ABNT
CARMONA, Rafaela Costa et al. 'A POT. 3'-coupling reaction as a strategy towards the synthesis of alkaloids. Journal of the Brazilian Chemical Society, v. 26, n. 1, p. 117-123, 2015Tradução . . Disponível em: http://www.scielo.br/pdf/jbchs/v26n1/0103-5053-jbchs-26-01-0117.pdf. Acesso em: 02 out. 2024. -
APA
Carmona, R. C., Wendler, E. P., Sakae, G. H., Comasseto, J. V., & Santos, A. A. dos. (2015). 'A POT. 3'-coupling reaction as a strategy towards the synthesis of alkaloids. Journal of the Brazilian Chemical Society, 26( 1), 117-123. Recuperado de http://www.scielo.br/pdf/jbchs/v26n1/0103-5053-jbchs-26-01-0117.pdf -
NLM
Carmona RC, Wendler EP, Sakae GH, Comasseto JV, Santos AA dos. 'A POT. 3'-coupling reaction as a strategy towards the synthesis of alkaloids [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 1): 117-123.[citado 2024 out. 02 ] Available from: http://www.scielo.br/pdf/jbchs/v26n1/0103-5053-jbchs-26-01-0117.pdf -
Vancouver
Carmona RC, Wendler EP, Sakae GH, Comasseto JV, Santos AA dos. 'A POT. 3'-coupling reaction as a strategy towards the synthesis of alkaloids [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 1): 117-123.[citado 2024 out. 02 ] Available from: http://www.scielo.br/pdf/jbchs/v26n1/0103-5053-jbchs-26-01-0117.pdf - The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction
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