Gotowa bibliografia na temat „Aza-lignans”
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Artykuły w czasopismach na temat "Aza-lignans"
Florent, Jean-Claude, Emmanuel Bertounesque, Matthieu Dorbec, Claude Monneret i Marie-Noëlle Rager. "Synthesis of γ-Lactam Lignans via Aza-Michael Addition". Synlett, nr 4 (2006): 0591–94. http://dx.doi.org/10.1055/s-2006-932485.
Pełny tekst źródłaBarker, David, Benjamin Dickson, Nora Dittrich i Claire E. Rye. "An acyl-Claisen approach to the synthesis of lignans and substituted pyrroles". Pure and Applied Chemistry 84, nr 7 (25.03.2012): 1557–65. http://dx.doi.org/10.1351/pac-con-11-09-27.
Pełny tekst źródłaOurhzif, El‐Mahdi, Arnaud Pâris, Isabelle Abrunhosa‐Thomas, El Mostafa Ketatni, Pierre Chalard, Mostafa Khouili, Richard Daniellou, Yves Troin i Mohamed Akssira. "Design, synthesis, and evaluation of cytotoxic activities of arylnaphthalene lignans and aza‐analogs". Archiv der Pharmazie 354, nr 6 (15.02.2021): 2000479. http://dx.doi.org/10.1002/ardp.202000479.
Pełny tekst źródłaHitotsuyanagi, Yukio, Masatsugu Kobayashi, Masamoto Fukuyo, Koichi Takeya i Hideji Itokawa. "A facile synthesis of the 4-aza-analogs of 1-arylnaphthalene lignans chinensin, justicidin B, and Taiwanin C". Tetrahedron Letters 38, nr 48 (grudzień 1997): 8295–96. http://dx.doi.org/10.1016/s0040-4039(97)10204-0.
Pełny tekst źródłaHITOTSUYANAGI, Y., M. KOBAYASHI, M. FUKUYO, K. TAKEYA i H. ITOKAWA. "ChemInform Abstract: A Facile Synthesis of the 4-Aza-Analogues of 1-Arylnaphthalene Lignans Chinensin, Justicidin B, and Taiwanin C." ChemInform 29, nr 7 (24.06.2010): no. http://dx.doi.org/10.1002/chin.199807171.
Pełny tekst źródłaDorbec, Matthieu, Jean-Claude Florent, Claude Monneret, Marie-Noelle Rager i Emmanuel Bertounesque. "Synthesis of γ-Lactam Lignans via Aza-Michael Addition." ChemInform 37, nr 28 (11.07.2006). http://dx.doi.org/10.1002/chin.200628207.
Pełny tekst źródłaXiang, Jia-Chen, Cédric Fung, Qian Wang i Jieping Zhu. "Taming the radical cation intermediate enabled one-step access to structurally diverse lignans". Nature Communications 13, nr 1 (16.06.2022). http://dx.doi.org/10.1038/s41467-022-31000-4.
Pełny tekst źródłaRozprawy doktorskie na temat "Aza-lignans"
Ourhzif, El-Mahdi. "Synthèse et évaluation pharmacologique de composés originaux de la famille des méthoxynaphtalènes et lignanes arylnaphtalènes à visée antitumorale". Electronic Thesis or Diss., Université Clermont Auvergne (2021-...), 2022. http://www.theses.fr/2022UCFAC016.
Pełny tekst źródłaBreast cancer is the most common malignant tumor in women, and the first in terms of incidence (2.1 million new cases worldwide in 2018). An increasing problem is the resistance of some cancer cells to different treatments. Due to its major impact on the population, this disease represents a critical public health problem that requires additional research at the molecular level in order to define specific therapies. The plant kingdom remains an essential source for many researchers in order to find new biologically active molecules, which can lead to the discovery of active ingredients. It is in this approach that the work carried out by our research group, in the field of the extraction and synthesis of analgesic and anticancer substances from plants used in traditional pharmacopoeia, led us to consider serial pharmacomodulations on analogues of « Guieranone A », a natural molecule isolated from the leaves of the Guiera senegalensis plant which is widely used in traditional African medicine for its therapeutic properties and which has remarkable antiproliferative activities on various tumor lines and in particular on breast cancer (MCF-7 hormone-dependent line, IC50 = 3.42 ± 0.090 µM). We have therefore developed a synthetic approach using 3,4-dimethoxy benzaldehyde as a starting material and involving Stobbe and Wittig-Horner-Emmons reactions. The synthetic reactions developed on this basis, as well as the molecules prepared, have opened a synthetic route to lignans and aza-lignans, compounds of biological and / or pharmacological interest well represented in many aromatic and medicinal plants (AMP), of the genus Justicia and Vitex. By this way, Justicidin C, Cilinaphthalide B, and Methoxy-vitedoamine A were prepared via a chloroformylation reaction followed by a Suzuki-Miyaura coupling reaction