Gotowa bibliografia na temat „Mitsunobu”
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Artykuły w czasopismach na temat "Mitsunobu"
Panday, Sharad Kumar. "Advances in the Mitsunobu Reaction: An Excellent Organic Protocol with Versatile Applications". Mini-Reviews in Organic Chemistry 16, nr 2 (4.01.2019): 127–40. http://dx.doi.org/10.2174/1570193x15666180612090313.
Pełny tekst źródłaHain, Julia, Patrick Rollin, Werner Klaffke i Thisbe K. Lindhorst. "Anomeric modification of carbohydrates using the Mitsunobu reaction". Beilstein Journal of Organic Chemistry 14 (29.06.2018): 1619–36. http://dx.doi.org/10.3762/bjoc.14.138.
Pełny tekst źródłaBianchi, Darío A., i Teodoro S. Kaufman. "A tosyliminium ion-based total synthesis of (±)-schefferine". Canadian Journal of Chemistry 78, nr 9 (1.09.2000): 1165–69. http://dx.doi.org/10.1139/v00-120.
Pełny tekst źródłaBut, Tracy Yuen Sze, i Patrick H. Toy. "Organocatalytic Mitsunobu Reactions". Journal of the American Chemical Society 128, nr 30 (sierpień 2006): 9636–37. http://dx.doi.org/10.1021/ja063141v.
Pełny tekst źródłaToy, P., i T. But. "Catalytic Mitsunobu Reaction". Synfacts 2006, nr 9 (wrzesień 2006): 0947. http://dx.doi.org/10.1055/s-2006-949230.
Pełny tekst źródłaDavey, Stephen. "Mitsunobu minus waste". Nature Chemistry 5, nr 5 (23.04.2013): 358. http://dx.doi.org/10.1038/nchem.1639.
Pełny tekst źródłaMunawar, Saba, Ameer Fawad Zahoor, Shafaqat Ali, Sadia Javed, Muhammad Irfan, Ali Irfan, Katarzyna Kotwica-Mojzych i Mariusz Mojzych. "Mitsunobu Reaction: A Powerful Tool for the Synthesis of Natural Products: A Review". Molecules 27, nr 20 (17.10.2022): 6953. http://dx.doi.org/10.3390/molecules27206953.
Pełny tekst źródłaCisneros Pérez, Pablo A., i Bernardo A. Fontana Uribe. "Síntesis de Sistemas bis-tiofénicos con puente α,α’-dioxi-m-xileno". Química Central 3, nr 2 (27.09.2017): 11–18. http://dx.doi.org/10.29166/quimica.v3i2.1208.
Pełny tekst źródłaHuang, Yangen, Roger W. Read i Xiaobei Wang. "Efficient Alkylation Methods for the Synthesis of Hybrid Fluorocarbon - Hydrocarbon Tetrazoles as Potential Fluorinated Surfactants". Australian Journal of Chemistry 63, nr 5 (2010): 802. http://dx.doi.org/10.1071/ch10005.
Pełny tekst źródłaKasama, Kengo. "Redox-neutral Mitsunobu Reaction". Journal of Synthetic Organic Chemistry, Japan 79, nr 4 (1.04.2021): 344–45. http://dx.doi.org/10.5059/yukigoseikyokaishi.79.344.
Pełny tekst źródłaRozprawy doktorskie na temat "Mitsunobu"
But, Yuen-sze Tracy, i 畢婉詩. "Organocatalytic alcohol oxidation and Mitsunobu reactions". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B42182578.
Pełny tekst źródłaBut, Yuen-sze Tracy. "Organocatalytic alcohol oxidation and Mitsunobu reactions". Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B42182578.
Pełny tekst źródłaCamp, David. "Some Aspects of the Mitsunobu Reaction". Thesis, Griffith University, 1990. http://hdl.handle.net/10072/366203.
Pełny tekst źródłaThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
Division of Science and Technology
Science, Environment, Engineering and Technology
Full Text
Shannon-Little, Andrew Laurence. "Studies towards a phosphorus(V)-catalysed Mitsunobu reaction". Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/33038/.
Pełny tekst źródłaLe, Foll Alexandra. "Polymères à empreintes moléculaires : nouveaux outils prometteurs pour la synthèse organique". Thesis, Rouen, INSA, 2010. http://www.theses.fr/2010ISAM0006.
Pełny tekst źródłaThis work deals with the use of molecular imprinting technology for the design of new tools in organic sythesis. First, we studied the potential of MIPs in organocatalysis through activation in the imprints. For this purpose, several thiourea-cinchona alkaloid derivatives have been prepared so as to be introduced in the polymer cavities. The use of different MIPs synthesised with these polymerisable catalysts in Henry reaction did not show any advantageous effect on reaction rate or enantioselectivity. Secondly, we have prformed the development of a strategy for separation and recovery of a wide range of compounds by relating tag technology with molecular imprinting. Efficiency and selectivity of MIP-Tag for in triazole series have been demonstrated. Tagged tyrosine has been selectively extracted from an amino-acid mixture. Then, the application of this Tag technology for the recovery of pybox and proline catalyst was investigated. Finally, we have demonstrated the efficiency of our process for the removal of triphenylphosphine oxide formed during a Mitsunobu reaction. The removal of 99% of tagged phosphine oxide was perforrmed by the purification of a reaction medium in SPE by means of MIP-Tag
Thompson, Stephen. "The synthesis of novel DNA-interactive pyrrolo-(2,1-c)[1,4]-benzodiazepin-5-ones". Thesis, University of Liverpool, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367072.
Pełny tekst źródłaSallas, Florence. "Méthodologies de fonctionnalisation directe, étude structurale et physico-chimique de nouveaux dérivés de cyclodextrines". Nancy 1, 1996. http://docnum.univ-lorraine.fr/public/SCD_T_1996_0398_SALLAS.pdf.
Pełny tekst źródłaFelten, Anne-Sophie. "Synthèse de N-aminopeptides. Application à la synthèse de nouveaux foldamères". Thesis, Vandoeuvre-les-Nancy, INPL, 2007. http://www.theses.fr/2007INPL095N/document.
Pełny tekst źródłaThis work describes the synthesis, the oligomerization and the structural study of N-aminopeptides. By extrapolating an original strategy of hydrazinoacids synthesis developed in the LCPM we were able to obtain N-aminodipeptides in high optical purity in a satisfactory way. These compounds were the indispensable precursors in order to continue the project. We were able to show that the activation of the acidic partner involved in the key reaction of Mitsunobu usually obtained by the use of the phtalimide group, could be advantageously realized by the introduction of a hydrazone moiety with strong electron-withdrawing character. An extension of this method on solid support is a result which constitutes an effective application of a Mitsunobu protocol in Solid Phase Organic Chemistry. The Naminodipeptides thus obtained were studied in reactions of oligomérisation. A preliminary study in liquid phase allowed to demonstrate that a classic peptidic coupling reaction could occur between two pseudopeptidic units. The continuation of the study was made on solid phase and allowed us to obtain the first [alpha-N-amino]peptides never synthesized to this day. Finally, in the third chapter, these oligomers were studied by molecular modelling and various spectroscopic methods (NMR, IR) who allowed to suggest a folding by the establishment of intramolecular hydrogen bonds
Fu, Jiasheng. "Investigation of stereoselection by the Mitsunobu reaction and modification of the Hendrickson reaction". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0009/NQ59960.pdf.
Pełny tekst źródłaBell, Kathryn Emma. "Advances in the retro-Cope elimination". Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307744.
Pełny tekst źródłaKsiążki na temat "Mitsunobu"
Kanō Mitsunobu no jidai. Tōkyō: Chūō Kōron Bijutsu Shuppan, 2007.
Znajdź pełny tekst źródłaTosa Mitsunobu and the small scroll in medieval Japan. Seattle: University of Washington Press, 2009.
Znajdź pełny tekst źródłaKenkyūkai, Ōsaka Shakai Jigyōshi, Ōsaka Jikyōkan i Yao Rinpokan, red. Yumi wa orezu: Nakamura Mitsunori to Ōsaka no shakai jigyō. Ōsaka-shi: Ōsaka Shakai Jigyōshi Kenkyūkai, 1985.
Znajdź pełny tekst źródłaCzęści książek na temat "Mitsunobu"
Laue, Thomas, i Andreas Plagens. "Mitsunobu-Reaktion". W Teubner Studienbücher Chemie, 227–30. Wiesbaden: Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-94015-5_72.
Pełny tekst źródłaLaue, Thomas, i Andreas Plagens. "Mitsunobu-Reaktion". W Teubner Studienbücher Chemie, 228–31. Wiesbaden: Vieweg+Teubner Verlag, 1998. http://dx.doi.org/10.1007/978-3-322-94077-3_73.
Pełny tekst źródłaLi, Jie Jack. "Mitsunobu reaction". W Name Reactions, 265. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_198.
Pełny tekst źródłaLaue, Thomas, i Andreas Plagens. "Mitsunobu-Reaktion". W Teubner Studienbücher Chemie, 227–30. Wiesbaden: Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-94726-0_72.
Pełny tekst źródłaLi, Jie Jack. "Mitsunobu reaction". W Name Reactions, 407–8. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_178.
Pełny tekst źródłaLi, Jie Jack. "Mitsunobu reaction". W Name Reactions, 238. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_187.
Pełny tekst źródłaLi, Jie Jack. "Mitsunobu reaction". W Name Reactions, 365–67. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_165.
Pełny tekst źródłaLi, Jie Jack. "Mitsunobu Reaction". W Name Reactions, 358–61. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_96.
Pełny tekst źródłaWang, Fengjiang, i James R. Hauske. "Solid-Phase Synthesis of Benzoxazoles via Mitsunobu Reaction". W Solid-Phase Organic Syntheses, 73–84. New York, USA: John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.ch7.
Pełny tekst źródłaTaniguchi, Tsuyoshi. "Mitsunobu Reactions in Medicinal Chemistry and Development of Practical Modifications". W Methods in Pharmacology and Toxicology, 97–122. New York, NY: Springer New York, 2021. http://dx.doi.org/10.1007/978-1-0716-1579-9_3.
Pełny tekst źródłaStreszczenia konferencji na temat "Mitsunobu"
Kozłowska, Mariola, i Zygmunt Kazimierczuk. "Synthesis of 2'-deoxyribonucleosides by the Mitsunobu reaction". W XIIIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2005. http://dx.doi.org/10.1135/css200507405.
Pełny tekst źródłaJulien Poupart, Julien Poupart, i William D. Lubell William D. Lubell. "Mitsunobu Reaction on Solid Support for Peptide N-terminal Farnesylation". W The 24th American Peptide Symposium. Prompt Scientific Publishing, 2015. http://dx.doi.org/10.17952/24aps.2015.094.
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