Gotowa bibliografia na temat „Electrophilic nitrogens”
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Artykuły w czasopismach na temat "Electrophilic nitrogens"
Aeyad, Tahani, Jason Williams, Anthony Meijer i Iain Coldham. "Lithiation–Substitution of N-Boc-2-phenylazepane". Synlett 28, nr 20 (17.08.2017): 2765–68. http://dx.doi.org/10.1055/s-0036-1590857.
Pełny tekst źródłaLEVONEN, Anna-Liisa, Aimee LANDAR, Anup RAMACHANDRAN, Erin K. CEASER, Dale A. DICKINSON, Giuseppe ZANONI, Jason D. MORROW i Victor M. DARLEY-USMAR. "Cellular mechanisms of redox cell signalling: role of cysteine modification in controlling antioxidant defences in response to electrophilic lipid oxidation products". Biochemical Journal 378, nr 2 (1.03.2004): 373–82. http://dx.doi.org/10.1042/bj20031049.
Pełny tekst źródłaCeaser, E. K., D. R. Moellering, S. Shiva, A. Ramachandran, A. Landar, A. Venkartraman, J. Crawford i in. "Mechanisms of signal transduction mediated by oxidized lipids: the role of the electrophile-responsive proteome". Biochemical Society Transactions 32, nr 1 (1.02.2004): 151–55. http://dx.doi.org/10.1042/bst0320151.
Pełny tekst źródłaPalillero-Cisneros, Angel, Paola G. Gordillo-Guerra, Fernando García-Alvarez, Olivier Jackowski, Franck Ferreira, Fabrice Chemla, Joel L. Terán i Alejandro Perez-Luna. "α-(Aminomethyl)acrylates as acceptors in radical–polar crossover 1,4-additions of dialkylzincs: insights into enolate formation and trapping". Beilstein Journal of Organic Chemistry 19 (21.09.2023): 1443–51. http://dx.doi.org/10.3762/bjoc.19.103.
Pełny tekst źródłaCao, Chengyao, Jinyu Sheng i Chao Chen. "Cu-Catalyzed Cascade Annulation of Diaryliodonium Salts and Nitriles: Synthesis of Nitrogen-Containing Heterocycles". Synthesis 49, nr 23 (11.10.2017): 5081–92. http://dx.doi.org/10.1055/s-0036-1589515.
Pełny tekst źródłaSlivka, Mikhailo, i Mikhailo Onysko. "The Use of Electrophilic Cyclization for the Preparation of Condensed Heterocycles". Synthesis 53, nr 19 (19.05.2021): 3497–512. http://dx.doi.org/10.1055/s-0040-1706036.
Pełny tekst źródłaChandra, Swaroop, B. Suryaprasad, N. Ramanathan i K. Sundararajan. "Nitrogen as a pnicogen?: evidence for π-hole driven novel pnicogen bonding interactions in nitromethane–ammonia aggregates using matrix isolation infrared spectroscopy and ab initio computations". Physical Chemistry Chemical Physics 23, nr 10 (2021): 6286–97. http://dx.doi.org/10.1039/d0cp06273a.
Pełny tekst źródłaBhadra, Biswa Nath, Yong Su Baek, Cheol Ho Choi i Sung Hwa Jhung. "How neutral nitrogen-containing compounds are oxidized in oxidative-denitrogenation of liquid fuel with TiO2@carbon". Physical Chemistry Chemical Physics 23, nr 14 (2021): 8368–74. http://dx.doi.org/10.1039/d1cp00633a.
Pełny tekst źródłaAgeshina, Alexandra A., Gleb A. Chesnokov, Maxim A. Topchiy, Igor V. Alabugin, Mikhail S. Nechaev i Andrey F. Asachenko. "Making endo-cyclizations favorable again: a conceptually new synthetic approach to benzotriazoles via azide group directed lithiation/cyclization of 2-azidoaryl bromides". Organic & Biomolecular Chemistry 17, nr 18 (2019): 4523–34. http://dx.doi.org/10.1039/c9ob00615j.
Pełny tekst źródłaShen, Kun, i Qiu Wang. "Copper-catalyzed diamination of unactivated alkenes with hydroxylamines". Chemical Science 6, nr 7 (2015): 4279–83. http://dx.doi.org/10.1039/c5sc00897b.
Pełny tekst źródłaRozprawy doktorskie na temat "Electrophilic nitrogens"
Blanc, Sylvain. "New reagents for asymmetric electrophilic nitrogen transfer". Thesis, Loughborough University, 2004. https://dspace.lboro.ac.uk/2134/34126.
Pełny tekst źródłaDaniel, Matthieu. "Nouvelles stratégies de synthèse d’hétérocycles polyazotés pour la conception de molécules énergétiques dérivées d’(aza)indazoles et de 1,3a,6a-triazapentalènes". Electronic Thesis or Diss., Orléans, 2019. http://www.theses.fr/2019ORLE3210.
Pełny tekst źródłaDue to their wide range of applications, the elaboration of original energetic materials represents an important part of research in organic chemistry. Besides, the stability and the high explosive performances of azaheterocycles, provided by their compact and nitrogen rich structures, make them promising candidates for energetic applications. Thus, the development of innovative methodologies is essential and remains very challenging. In this context, we aimed at developing new methodologies to access functionalized nitrogen rich heterocycles. For this purpose, we first investigated a recent strategy giving access to polynitrated (aza)indazoles via a Staudinger/aza-Wittig tandem reaction. A second part was dedicated to the development of an original way to synthesize tricyclic triazapentalene derivatives from non-hazardous and readily available precursors. The generation of electrophilic nitrogen, essential to achieve this transformation, was ensured by various heteroaryl amines in presence of hypervalent iodine in mild conditions.The last part of this work focused on the application of these strategies to access new energetic materials
Cino, Silvia <1985>. "Coupling Reactions Between Aromatic Carbon - and Nitrogen - Nucleophiles and Electrophiles: Reaction Intermediates, Products and their Properties". Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amsdottorato.unibo.it/7566/1/TESI_DOTTORATO_CinoSilvia.pdf.
Pełny tekst źródłaCino, Silvia <1985>. "Coupling Reactions Between Aromatic Carbon - and Nitrogen - Nucleophiles and Electrophiles: Reaction Intermediates, Products and their Properties". Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amsdottorato.unibo.it/7566/.
Pełny tekst źródłaEichman, Chad. "Development of Electrophilic Amination with Oximes for the Synthesis of Nitrogen-Containing Heterocycles; Transition Metal Catalysts for Carbon-Sulfur and Carbon-Carbon Bond Formation and Selective C-H Activation". The Ohio State University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=osu1275430570.
Pełny tekst źródłaEL, ALAMI NAJAT. "Isolement et reactivite du derive zincique de (bromomethyl-2) acrylate d'ethyle : synthese de methylene-3 pyrrolidinone-3 potentiellement antineoplasique". Nantes, 1987. http://www.theses.fr/1987NANT2016.
Pełny tekst źródłaBerkaoui, M'hamed. "Réactivité énaminique de β-aminothiophènes vis-à-vis de divers électrophiles. Accès à des hétérocycles thiophéniques azotés". Rouen, 1998. http://www.theses.fr/1998ROUES015.
Pełny tekst źródłaCouture, Karine. "Etude de la métallation en série diazinique 1) premier échange iode-lithium avec les alkylamidures de lithium 2) amination électrophile 3) première métallation sans groupe directeur". Rouen, 1995. http://www.theses.fr/1995ROUES020.
Pełny tekst źródłaDebleds, François. "Complexation d'électrophiles aromatiques par des bases hétérocycliques ambidentes : structure et réactivité d'adduits carbones et azotes pyrroliques indoliques et imidazoliques". Paris 6, 1987. http://www.theses.fr/1987PA066330.
Pełny tekst źródłaJacquelin, Jean-Marie. "Fonctionnalisation par métallation d'amino et d'hydroxy quinoléines : applications à la synthèse de furo quinoléines". Rouen, 1987. http://www.theses.fr/1987ROUES033.
Pełny tekst źródłaCzęści książek na temat "Electrophilic nitrogens"
Beak, Peter, Timothy A. Johnson, Dwight D. Kim i Sung H. Lim. "Enantioselective Synthesis by Lithiation Adjacent to Nitrogen and Electrophile Incorporation". W Organolithiums in Enantioselective Synthesis, 139–76. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/3-540-36117-0_5.
Pełny tekst źródłaBeaulieu, Pierre l., i robert dáziel. "Addition of electrophilic organoselenium reagents to carbon-carbon double bonds". W Organoselenium Chemistry, 35–66. Oxford University PressOxford, 1999. http://dx.doi.org/10.1093/oso/9780198501411.003.0003.
Pełny tekst źródłaXiong, T., i Y. Li. "1.2 Copper(I) Hydride Catalyzed Transformations". W Base-Metal Catalysis 1. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-238-00029.
Pełny tekst źródłaDavies, David T. "Indoles". W Aromatic Heterocyclic Chemistry. Oxford University Press, 1992. http://dx.doi.org/10.1093/hesc/9780198556602.003.0007.
Pełny tekst źródłaGrimmett, M. R. "Electrophilic Displacement". W Five-Membered Hetarenes with Two Nitrogen or Phosphorus Atoms, 1. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-012-00750.
Pełny tekst źródłaHajos, G., i Z. Riedl. "Electrophilic Substitution". W Five-Membered Hetarenes with Two Nitrogen or Phosphorus Atoms, 1. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-012-00854.
Pełny tekst źródłaLarsen, R. D., i D. Cai. "Electrophilic Acylation". W Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00816.
Pełny tekst źródłalvarez, M., i J. A. Joule. "Electrophilic Acylation". W Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01287.
Pełny tekst źródłalvarez, M., i J. A. Joule. "Electrophilic Substitution". W Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01296.
Pełny tekst źródłalvarez, M., i J. A. Joule. "Electrophilic Alkylation". W Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01469.
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