Literatura científica selecionada sobre o tema "Metallotropic rearrangement"
Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos
Consulte a lista de atuais artigos, livros, teses, anais de congressos e outras fontes científicas relevantes para o tema "Metallotropic rearrangement".
Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.
Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.
Artigos de revistas sobre o assunto "Metallotropic rearrangement"
Zambon, Alfonso, Giuseppe Borsato, Stefania Brussolo, Pietrogiulio Frascella e Vittorio Lucchini. "Efficient access to 5-substituted thiazoles by a novel metallotropic rearrangement". Tetrahedron Letters 49, n.º 1 (janeiro de 2008): 66–69. http://dx.doi.org/10.1016/j.tetlet.2007.11.029.
Texto completo da fonteYezernitskaya, M. G., B. V. Lokshin, V. I. Zdanovich, I. A. Lobanova e N. E. Kolobova. "Metallotropic η5 → η6 rearrangement in indenyltricarbonyl complexes of manganese and rhenium in an acid medium". Journal of Organometallic Chemistry 282, n.º 3 (março de 1985): 363–68. http://dx.doi.org/10.1016/0022-328x(85)87195-3.
Texto completo da fonteSèbe, Gilles, e Bernard De Jéso. "The Dimensional Stabilisation of Maritime Pine Sapwood (Pinus pinaster) by Chemical Reaction with Organosilicon Compounds". Holzforschung 54, n.º 5 (6 de setembro de 2000): 474–80. http://dx.doi.org/10.1515/hf.2000.080.
Texto completo da fonteOprunenko, Yu F., I. A. Shaposhnikova, Yu A. Ustynyuk, N. A. Ustynyuk e D. N. Kravtsov. "Metallotropic rearrangements in biphenylchromium tricarbonyl complexes". Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, n.º 3 (março de 1987): 644. http://dx.doi.org/10.1007/bf00955875.
Texto completo da fonteOprunenko, Yuri, Svetlana Malyugina, Pavel Nesterenko, Dmitry Mityuk e Oleg Malyshev. "Intramolecular versus intermolecular mechanism of metallotropic rearrangements of chiral chromium tricarbonyl complexes of substituted naphthalenes and other polyaromatic compounds investigated by chiral HPLC of its racemic mixtures". Journal of Organometallic Chemistry 597, n.º 1-2 (março de 2000): 42–47. http://dx.doi.org/10.1016/s0022-328x(99)00573-2.
Texto completo da fonteZambon, Alfonso, Giuseppe Borsato, Stefania Brussolo, Pietrogiulio Frascella e Vittorio Lucchini. "ChemInform Abstract: Efficient Access to 5-Substituted Thiazoles by a Novel Metallotropic Rearrangement." ChemInform 39, n.º 15 (8 de abril de 2008). http://dx.doi.org/10.1002/chin.200815126.
Texto completo da fonteOPRUNENKO, YU F., I. A. SHAPOSHNIKOVA, YU A. USTYNYUK, N. A. USTYNYUK e D. N. KRAVTSOV. "ChemInform Abstract: Metallotropic Rearrangements in Biphenylchromium Tricarbonyl Complexes." ChemInform 18, n.º 42 (20 de outubro de 1987). http://dx.doi.org/10.1002/chin.198742279.
Texto completo da fonteTeses / dissertações sobre o assunto "Metallotropic rearrangement"
Pierret, Alexandre. "Fonctionnalisation à distance par métallotropie de dérivés benzyliques". Electronic Thesis or Diss., Université de Lorraine, 2023. https://docnum.univ-lorraine.fr/ulprive/DDOC_T_2023_0032_PIERRET.pdf.
Texto completo da fonteThis thesis presents a development of the remote functionalization reaction by metallotropic rearrangement on benzyl derivatives. The work is based on the use of a single metal reagent, a lithium triorganozincate, which allows the formation of two bonds C(sp3)-C(sp2) and C(sp3)-C(sp3) on sites 5 atoms apart in a single operation. The first chapter focuses on benzyl derivatives with an iodine in position 4 of the aromatic ring. Novel reaction conditions based on the use of a bio-based solvent are proposed. They allow to reach an unprecedented synthetic scope for such a reaction from these substrates. The influence of the solvent is also discussed. The second chapter is devoted to the mechanistic study by DFT of each step composing the reaction sequence studied previously. Thus, the halogen/metal exchange, the 1,2-migration of ligand or the metallotropic rearrangement are investigated with careful consideration of the solvent of the reaction. An experimental contribution completes this study. Finally, the extension of this transformation to benzylic heteroaromatic derivatives, in particular thiophenes, is the subject of the last chapter of this thesis. The reported work defines an approach of remote functionalization where a same toolbox, composed of a unique platform (halogenated thiophene bearing a benzyl phosphate) and an organometallic reagent of the same nature (lithium organozincate), offers several synthetic opportunities according to the experimenter's desires