An experimental and theoretical study into the facile, homogenous (N-heterocyclic carbene)2- Pd(0) catalyzed diboration of internal and terminal alkynes (2016)
- Authors:
- Autor USP: BRAGA, ATAUALPA ALBERT CARMO - IQ
- Unidade: IQ
- DOI: 10.1039/c6cy01266c
- Subjects: CATÁLISE; QUÍMICA QUÂNTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Catalysis Science and Technology
- ISSN: 2044-4753
- Volume/Número/Paginação/Ano: p. 1-7, 2016
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
ANSELL, Melvyn B et al. An experimental and theoretical study into the facile, homogenous (N-heterocyclic carbene)2- Pd(0) catalyzed diboration of internal and terminal alkynes. Catalysis Science and Technology, p. 1-7, 2016Tradução . . Disponível em: https://doi.org/10.1039/c6cy01266c. Acesso em: 23 jan. 2026. -
APA
Ansell, M. B., Silva, V. H. M. da, Heerdt, G., Braga, A. A. C., Spencer, J., & Navarro, O. (2016). An experimental and theoretical study into the facile, homogenous (N-heterocyclic carbene)2- Pd(0) catalyzed diboration of internal and terminal alkynes. Catalysis Science and Technology, 1-7. doi:10.1039/c6cy01266c -
NLM
Ansell MB, Silva VHM da, Heerdt G, Braga AAC, Spencer J, Navarro O. An experimental and theoretical study into the facile, homogenous (N-heterocyclic carbene)2- Pd(0) catalyzed diboration of internal and terminal alkynes [Internet]. Catalysis Science and Technology. 2016 ; 1-7.[citado 2026 jan. 23 ] Available from: https://doi.org/10.1039/c6cy01266c -
Vancouver
Ansell MB, Silva VHM da, Heerdt G, Braga AAC, Spencer J, Navarro O. An experimental and theoretical study into the facile, homogenous (N-heterocyclic carbene)2- Pd(0) catalyzed diboration of internal and terminal alkynes [Internet]. Catalysis Science and Technology. 2016 ; 1-7.[citado 2026 jan. 23 ] Available from: https://doi.org/10.1039/c6cy01266c - Experimental and quantum chemical approaches for Hydrazide-based crystalline organic chromophores: synthesis, SC-XRD, spectroscopic and nonlinear optical properties
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Informações sobre o DOI: 10.1039/c6cy01266c (Fonte: oaDOI API)
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