Mild and selective transformations of amines and alcohols through bioinspired oxidation with nitrous oxide or oxygen (2024)
- Authors:
- Autor USP: ANDRADE, LEANDRO HELGUEIRA DE - IQ
- Unidade: IQ
- DOI: 10.1039/d3cy01635h
- Subjects: OXIGÊNIO; AMINAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Catalysis Science and Technology
- ISSN: 2044-4753
- Volume/Número/Paginação/Ano: v., 14, p. 1512-1523, 2024
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by-nc
-
ABNT
SACCHELLI, Bruce Alan Lobo et al. Mild and selective transformations of amines and alcohols through bioinspired oxidation with nitrous oxide or oxygen. Catalysis Science and Technology, p. 1512-1523, 2024Tradução . . Disponível em: https://dx.doi.org/10.1039/d3cy01635h. Acesso em: 27 abr. 2024. -
APA
Sacchelli, B. A. L., Almeida, R. S. M., Mahmoud, A. G., Nesterov, D. S., Andrade, L. H., Phillips, A. M. M. F., et al. (2024). Mild and selective transformations of amines and alcohols through bioinspired oxidation with nitrous oxide or oxygen. Catalysis Science and Technology, 1512-1523. doi:10.1039/d3cy01635h -
NLM
Sacchelli BAL, Almeida RSM, Mahmoud AG, Nesterov DS, Andrade LH, Phillips AMMF, Alegria ECBA, Prechtl MHG. Mild and selective transformations of amines and alcohols through bioinspired oxidation with nitrous oxide or oxygen [Internet]. Catalysis Science and Technology. 2024 ; 1512-1523.[citado 2024 abr. 27 ] Available from: https://dx.doi.org/10.1039/d3cy01635h -
Vancouver
Sacchelli BAL, Almeida RSM, Mahmoud AG, Nesterov DS, Andrade LH, Phillips AMMF, Alegria ECBA, Prechtl MHG. Mild and selective transformations of amines and alcohols through bioinspired oxidation with nitrous oxide or oxygen [Internet]. Catalysis Science and Technology. 2024 ; 1512-1523.[citado 2024 abr. 27 ] Available from: https://dx.doi.org/10.1039/d3cy01635h - 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
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Informações sobre o DOI: 10.1039/d3cy01635h (Fonte: oaDOI API)
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