Literatura académica sobre el tema "Mitsunobu reaction"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte las listas temáticas de artículos, libros, tesis, actas de conferencias y otras fuentes académicas sobre el tema "Mitsunobu reaction".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Artículos de revistas sobre el tema "Mitsunobu reaction"
Panday, Sharad Kumar. "Advances in the Mitsunobu Reaction: An Excellent Organic Protocol with Versatile Applications". Mini-Reviews in Organic Chemistry 16, n.º 2 (4 de enero de 2019): 127–40. http://dx.doi.org/10.2174/1570193x15666180612090313.
Texto completoToy, P. y T. But. "Catalytic Mitsunobu Reaction". Synfacts 2006, n.º 9 (septiembre de 2006): 0947. http://dx.doi.org/10.1055/s-2006-949230.
Texto completoHain, Julia, Patrick Rollin, Werner Klaffke y Thisbe K. Lindhorst. "Anomeric modification of carbohydrates using the Mitsunobu reaction". Beilstein Journal of Organic Chemistry 14 (29 de junio de 2018): 1619–36. http://dx.doi.org/10.3762/bjoc.14.138.
Texto completoKasama, Kengo. "Redox-neutral Mitsunobu Reaction". Journal of Synthetic Organic Chemistry, Japan 79, n.º 4 (1 de abril de 2021): 344–45. http://dx.doi.org/10.5059/yukigoseikyokaishi.79.344.
Texto completoLongwitz, Lars y Thomas Werner. "The Mitsunobu reaction, reimagined". Science 365, n.º 6456 (29 de agosto de 2019): 866–67. http://dx.doi.org/10.1126/science.aay6635.
Texto completoBoyle, Benjamin T., Kyle G. Nottingham y Andrew McNally. "An Organocatalytic Mitsunobu Reaction". Trends in Chemistry 2, n.º 2 (febrero de 2020): 174–75. http://dx.doi.org/10.1016/j.trechm.2019.11.001.
Texto completoMunawar, Saba, Ameer Fawad Zahoor, Shafaqat Ali, Sadia Javed, Muhammad Irfan, Ali Irfan, Katarzyna Kotwica-Mojzych y Mariusz Mojzych. "Mitsunobu Reaction: A Powerful Tool for the Synthesis of Natural Products: A Review". Molecules 27, n.º 20 (17 de octubre de 2022): 6953. http://dx.doi.org/10.3390/molecules27206953.
Texto completoJia, Zhaozhong J., Sandra Kelberlau, Lars Olsson, G. Anilkumar y Bert Fraser-Reid. "The Mitsunobu Reaction of Tetrachlorophthalimide". Synlett 1999, n.º 5 (mayo de 1999): 565–66. http://dx.doi.org/10.1055/s-1999-2680.
Texto completoMarkowicz, Marcin W. y Roman Dembinski. "Fluorous, Chromatography-Free Mitsunobu Reaction". Organic Letters 4, n.º 22 (octubre de 2002): 3785–87. http://dx.doi.org/10.1021/ol0264511.
Texto completoHUGHES, D. L. "ChemInform Abstract: The Mitsunobu Reaction". ChemInform 25, n.º 44 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199444253.
Texto completoTesis sobre el tema "Mitsunobu reaction"
Camp, David. "Some Aspects of the Mitsunobu Reaction". Thesis, Griffith University, 1990. http://hdl.handle.net/10072/366203.
Texto completoThesis (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/.
Texto completoFu, 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.
Texto completoBell, Kathryn Emma. "Advances in the retro-Cope elimination". Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307744.
Texto completoFelten, 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.
Texto completoThis 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
Fairfull-Smith, Kathryn Elizabeth y n/a. "Synthetic and Mechanistic Investigations of Some Novel Organophosphorus Reagents". Griffith University. School of Science, 2004. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20040917.081950.
Texto completoFairfull-Smith, Kathryn Elizabeth. "Synthetic and Mechanistic Investigations of Some Novel Organophosphorus Reagents". Thesis, Griffith University, 2004. http://hdl.handle.net/10072/367534.
Texto completoThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Science
Full Text
Woods, Timothy E. "Elucidating the degree of selectivity for NLO surrogate attachment to model compounds and a co-polyimide using the Mitsunobu reaction /". Online version of thesis, 2008. http://hdl.handle.net/1850/7725.
Texto completoAzzouz, Rabah. "Pyridinols protégés et leur utilisation en métallation. Synthèse d'indolizidines à partir de la pyridine : synthèse d'indolizidines à partir de la pyridine". Phd thesis, INSA de Rouen, 2008. http://tel.archives-ouvertes.fr/tel-00559656.
Texto completoFang, Fang. "Synthesis of Bicyclic and Tricyclic Analogues of Oxazolidinone". Ohio University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1357312054.
Texto completoCapítulos de libros sobre el tema "Mitsunobu reaction"
Li, Jie Jack. "Mitsunobu reaction". En Name Reactions, 265. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_198.
Texto completoLi, Jie Jack. "Mitsunobu reaction". En Name Reactions, 407–8. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_178.
Texto completoLi, Jie Jack. "Mitsunobu reaction". En Name Reactions, 238. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_187.
Texto completoLi, Jie Jack. "Mitsunobu reaction". En Name Reactions, 365–67. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_165.
Texto completoLi, Jie Jack. "Mitsunobu Reaction". En Name Reactions, 358–61. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_96.
Texto completoWang, Fengjiang y James R. Hauske. "Solid-Phase Synthesis of Benzoxazoles via Mitsunobu Reaction". En Solid-Phase Organic Syntheses, 73–84. New York, USA: John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.ch7.
Texto completoMalkinson, John P. y Robert A. Falconer. "Solid-Phase Synthesis of Thio-Linked C-Terminal Glycopeptides via a Mitsunobu Reaction". En Peptides: The Wave of the Future, 506–7. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_234.
Texto completoTaniguchi, Tsuyoshi. "Mitsunobu Reactions in Medicinal Chemistry and Development of Practical Modifications". En 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.
Texto completoGriesbeck, A. G. y T. Sokolova. "Mitsunobu Reaction". En Ethers, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-037-00252.
Texto completo"61. Mitsunobu Reaction". En Organic Chemistry: 100 Must-Know Mechanisms, 136–37. De Gruyter, 2020. http://dx.doi.org/10.1515/9783110608373-061.
Texto completoActas de conferencias sobre el tema "Mitsunobu reaction"
Kozłowska, Mariola y Zygmunt Kazimierczuk. "Synthesis of 2'-deoxyribonucleosides by the Mitsunobu reaction". En 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.
Texto completoJulien Poupart, Julien Poupart y William D. Lubell William D. Lubell. "Mitsunobu Reaction on Solid Support for Peptide N-terminal Farnesylation". En The 24th American Peptide Symposium. Prompt Scientific Publishing, 2015. http://dx.doi.org/10.17952/24aps.2015.094.
Texto completo