ReP USP - Resultado da busca

Filtros : " IQ011" "Reino Unido" Removidos: "Direito do Estado" "Universidade Federal do Rio Grande do Norte (UFRN)" "Ferraz, José Bento Sterman" "CURI, RUI" "Financiado pelo FEDER" 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: 19 nov. 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 nov. 19 ] 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 nov. 19 ] 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: 19 nov. 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 nov. 19 ] 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 nov. 19 ] Available from: https://doi.org/10.1039/c5ra06469d

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