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Filtros : " IQ011" "Reino Unido" Removidos: "IFSC006" "Costa, Luciano da Fontoura" "Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)" Limpar

Filtros

Artigo de periodico
Catalytic oxidation of cinnamyl alcohol using 'AU'-'AG' nanotubes investigated by surface-enhanced Raman spectroscopy (2015)
Costa, Jean Claudio Santos; Corio, Paola ; Rossi, Liane Marcia
Source: Nanoscale. Unidade: IQ
Subjects: ESPECTROSCOPIA RAMAN, NANOTECNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Jean Claudio Santos e CORIO, Paola e ROSSI, Liane Marcia. Catalytic oxidation of cinnamyl alcohol using 'AU'-'AG' nanotubes investigated by surface-enhanced Raman spectroscopy. Nanoscale, v. 7, n. 18, p. 8536-8543, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5nr01064k. Acesso em: 04 out. 2024.
APA
Costa, J. C. S., Corio, P., & Rossi, L. M. (2015). Catalytic oxidation of cinnamyl alcohol using 'AU'-'AG' nanotubes investigated by surface-enhanced Raman spectroscopy. Nanoscale, 7( 18), 8536-8543. doi:10.1039/c5nr01064k
NLM
Costa JCS, Corio P, Rossi LM. Catalytic oxidation of cinnamyl alcohol using 'AU'-'AG' nanotubes investigated by surface-enhanced Raman spectroscopy [Internet]. Nanoscale. 2015 ; 7( 18): 8536-8543.[citado 2024 out. 04 ] Available from: https://doi.org/10.1039/c5nr01064k
Vancouver
Costa JCS, Corio P, Rossi LM. Catalytic oxidation of cinnamyl alcohol using 'AU'-'AG' nanotubes investigated by surface-enhanced Raman spectroscopy [Internet]. Nanoscale. 2015 ; 7( 18): 8536-8543.[citado 2024 out. 04 ] Available from: https://doi.org/10.1039/c5nr01064k
Artigo de periodico
Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols (2015)
Martins, Rodrigo S; Ahmad, Anees; Silva Junior, Luiz Fernando da; Andrade, Leandro Helgueira
Source: RSC Advances. Unidade: IQ
Subjects: LIPASE, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTINS, Rodrigo S et al. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols. RSC Advances, v. 5, n. 70, p. 56599-56605, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5ra06469d. Acesso em: 04 out. 2024.
APA
Martins, R. S., Ahmad, A., Silva Junior, L. F. da, & Andrade, L. H. (2015). Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols. RSC Advances, 5( 70), 56599-56605. doi:10.1039/c5ra06469d
NLM
Martins RS, Ahmad A, Silva Junior LF da, Andrade LH. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols [Internet]. RSC Advances. 2015 ; 5( 70): 56599-56605.[citado 2024 out. 04 ] Available from: https://doi.org/10.1039/c5ra06469d
Vancouver
Martins RS, Ahmad A, Silva Junior LF da, Andrade LH. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols [Internet]. RSC Advances. 2015 ; 5( 70): 56599-56605.[citado 2024 out. 04 ] Available from: https://doi.org/10.1039/c5ra06469d

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