Martins, Rodrigo S; Ahmad, Anees; Silva Junior, Luiz Fernando da; Andrade, Leandro Helgueira 
Fonte: RSC Advances. Unidade: IQ
Assuntos: LIPASE, SÍNTESE ORGÂNICA
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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: 06 ago. 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/c5ra06469dNLM
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 ago. 06 ] Available from: https://doi.org/10.1039/c5ra06469dVancouver
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 ago. 06 ] Available from: https://doi.org/10.1039/c5ra06469d
