Enzymatic kinetic resolution of tert-butyl 2-(1-hydroxyethyl)phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes (2011)
- Authors:
- Autor USP: ANDRADE, LEANDRO HELGUEIRA DE - IQ
- Unidade: IQ
- DOI: 10.3390/molecules16098098
- Subjects: ÁLCOOL; LIPASE
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
PIOVAN, Leandro e PASQUINI, Mônica D´Arcadia e ANDRADE, Leandro Helgueira. Enzymatic kinetic resolution of tert-butyl 2-(1-hydroxyethyl)phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes. Molecules, v. 16, n. 9, p. 8098-8109, 2011Tradução . . Disponível em: https://doi.org/10.3390/molecules16098098. Acesso em: 18 abr. 2024. -
APA
Piovan, L., Pasquini, M. D. ´A., & Andrade, L. H. (2011). Enzymatic kinetic resolution of tert-butyl 2-(1-hydroxyethyl)phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes. Molecules, 16( 9), 8098-8109. doi:10.3390/molecules16098098 -
NLM
Piovan L, Pasquini MD´A, Andrade LH. Enzymatic kinetic resolution of tert-butyl 2-(1-hydroxyethyl)phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes [Internet]. Molecules. 2011 ; 16( 9): 8098-8109.[citado 2024 abr. 18 ] Available from: https://doi.org/10.3390/molecules16098098 -
Vancouver
Piovan L, Pasquini MD´A, Andrade LH. Enzymatic kinetic resolution of tert-butyl 2-(1-hydroxyethyl)phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes [Internet]. Molecules. 2011 ; 16( 9): 8098-8109.[citado 2024 abr. 18 ] Available from: https://doi.org/10.3390/molecules16098098 - Magnetic bio-nanocomposite catalysts of 'CO''FE IND. 2''O IND. 4'/hydroxyapatite-lipase for enantioselective synthesis provide a framework for enzyme recovery and reuse
- Enzymatic reactions involving the heteroatoms from organic substrates
- Studies on terrein as a new class of proteasome inhibitors
- Síntese assimétrica de organoseleno aminas
- Hidrólise enantiosseletiva de 'beta'-boril-ésteres mediada por lipases
- Oxidation of organoselenium compounds: a study of chemoselectivity of phenylacetone monooxygenase
- Exploiting the enantioselectivity of Baeyer-Villiger monooxygenases via boron oxidation
- Synthesis of chiral organic selenium and tellurium compounds. The role of biocatalysis
- The 20s proteasome as target for antitumoral compounds: screenning for selective and reversible inhibitors among fungi-derived metabolites
- Resolução cinética de alcoóis primários através de reação de transesterificação catalisada por lipases
Informações sobre o DOI: 10.3390/molecules16098098 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
