Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins (2018)
- Autores:
- Autor USP: BRAGA, ATAUALPA ALBERT CARMO - IQ
- Unidade: IQ
- DOI: 10.1002/chem.201801910
- Assuntos: CATÁLISE; PALÁDIO
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Chemistry European Journal
- ISSN: 0947-6539
- Volume/Número/Paginação/Ano: v. 24, n. 45, p.11738-11747, 2018
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
OLIVEIRA, Juliana Manso de et al. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins. Chemistry European Journal, v. 24, n. 45, p. 11738-11747, 2018Tradução . . Disponível em: https://doi.org/10.1002/chem.201801910. Acesso em: 16 abr. 2024. -
APA
Oliveira, J. M. de, Angnes, R. A., Khan, I. U., Polo, E. C., Heerdt, G., Servilha, B. M., et al. (2018). Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins. Chemistry European Journal, 24( 45), 11738-11747. doi:10.1002/chem.201801910 -
NLM
Oliveira JM de, Angnes RA, Khan IU, Polo EC, Heerdt G, Servilha BM, Silva VHM da, Braga AAC, Correia CRD. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins [Internet]. Chemistry European Journal. 2018 ; 24( 45): 11738-11747.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1002/chem.201801910 -
Vancouver
Oliveira JM de, Angnes RA, Khan IU, Polo EC, Heerdt G, Servilha BM, Silva VHM da, Braga AAC, Correia CRD. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins [Internet]. Chemistry European Journal. 2018 ; 24( 45): 11738-11747.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1002/chem.201801910 - Synthesis, single crystal analysis and DFT based computational studies of 2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrim idin-1-ium 3,4,5- trihydroxybenzoate -methanol (DETM)
- Estudo computacional do mecanismo de reação da formação de aril alquil éteres catalisada por complexos de paládio
- O-4-Acetylamino-benzenesulfonylated pyrimidine derivatives: synthesis, SC-XRD, DFT analysis and electronic behaviour investigation
- Exploration of chromone-based thiosemicarbazone derivatives: SC-XRD/DFT, spectral (IR, UV–Vis) characterization, and quantum chemical analysis
- Highly efficient one pot palladium-catalyzed synthesis of 3,5-bis (arylated) pyridines: Comparative experimental and DFT studies
- Synthetic, XRD, non-covalent interactions and solvent dependent nonlinear optical studies of Sulfadiazine-Ortho-Vanillin Schiff base: (E)-4-((2-hydroxy-3-methoxy- benzylidene) amino)-N-(pyrimidin-2-yl)benzene-sulfonamide
- Homogeneous computational catalysis: The mechanism for cross-coupling and other C-C bond formation processes
- Investigação teórica sobre a etapa de adição oxidativa dos ciclos catalíticos das reações de Heck-Matsuda e Heck-Mizoroki
- Synthesis of novel (N-heterocyclic carbene) palladate complexes and their catalytic activity
- The role of cyclobutenes in gold(I)-catalysed skeletal rearrangement of 1,6-enynes
Informações sobre o DOI: 10.1002/chem.201801910 (Fonte: oaDOI API)
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas