Gotowa bibliografia na temat „Mitsunobu reaction”
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Artykuły w czasopismach na temat "Mitsunobu reaction"
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 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 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 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 źródłaLongwitz, Lars, i Thomas Werner. "The Mitsunobu reaction, reimagined". Science 365, nr 6456 (29.08.2019): 866–67. http://dx.doi.org/10.1126/science.aay6635.
Pełny tekst źródłaBoyle, Benjamin T., Kyle G. Nottingham i Andrew McNally. "An Organocatalytic Mitsunobu Reaction". Trends in Chemistry 2, nr 2 (luty 2020): 174–75. http://dx.doi.org/10.1016/j.trechm.2019.11.001.
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 źródłaJia, Zhaozhong J., Sandra Kelberlau, Lars Olsson, G. Anilkumar i Bert Fraser-Reid. "The Mitsunobu Reaction of Tetrachlorophthalimide". Synlett 1999, nr 5 (maj 1999): 565–66. http://dx.doi.org/10.1055/s-1999-2680.
Pełny tekst źródłaMarkowicz, Marcin W., i Roman Dembinski. "Fluorous, Chromatography-Free Mitsunobu Reaction". Organic Letters 4, nr 22 (październik 2002): 3785–87. http://dx.doi.org/10.1021/ol0264511.
Pełny tekst źródłaHUGHES, D. L. "ChemInform Abstract: The Mitsunobu Reaction". ChemInform 25, nr 44 (18.08.2010): no. http://dx.doi.org/10.1002/chin.199444253.
Pełny tekst źródłaRozprawy doktorskie na temat "Mitsunobu reaction"
Camp, 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 źródłaFu, 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 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
Fairfull-Smith, Kathryn Elizabeth, i 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.
Pełny tekst źródłaFairfull-Smith, Kathryn Elizabeth. "Synthetic and Mechanistic Investigations of Some Novel Organophosphorus Reagents". Thesis, Griffith University, 2004. http://hdl.handle.net/10072/367534.
Pełny tekst źródłaThesis (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.
Pełny tekst źródłaAzzouz, 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.
Pełny tekst źródłaFang, Fang. "Synthesis of Bicyclic and Tricyclic Analogues of Oxazolidinone". Ohio University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1357312054.
Pełny tekst źródłaCzęści książek na temat "Mitsunobu reaction"
Li, 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 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 źródłaMalkinson, John P., i Robert A. Falconer. "Solid-Phase Synthesis of Thio-Linked C-Terminal Glycopeptides via a Mitsunobu Reaction". W Peptides: The Wave of the Future, 506–7. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_234.
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 źródłaGriesbeck, A. G., i T. Sokolova. "Mitsunobu Reaction". W Ethers, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-037-00252.
Pełny tekst źródła"61. Mitsunobu Reaction". W Organic Chemistry: 100 Must-Know Mechanisms, 136–37. De Gruyter, 2020. http://dx.doi.org/10.1515/9783110608373-061.
Pełny tekst źródłaStreszczenia konferencji na temat "Mitsunobu reaction"
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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