Gotowa bibliografia na temat „Absolute asymmetric catalysis”
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Artykuły w czasopismach na temat "Absolute asymmetric catalysis"
Kaupp, Gerd, i Michael Haak. "Absolute Asymmetric Synthesis by Irradiation of Chiral Crystals". Angewandte Chemie International Edition in English 32, nr 5 (maj 1993): 694–95. http://dx.doi.org/10.1002/anie.199306941.
Pełny tekst źródłaLin, Yun-Ming, Zhongtao Li i Julie Boucau. "Predicting the R/S absolute configuration in asymmetric bifunctional catalysis (ABC)". Tetrahedron Letters 48, nr 30 (lipiec 2007): 5275–78. http://dx.doi.org/10.1016/j.tetlet.2007.05.131.
Pełny tekst źródłaBuchcic-Szychowska, Aleksandra, Anna Zawisza, Stanisław Leśniak i Michał Rachwalski. "Highly Efficient Asymmetric Morita–Baylis–Hillman Reaction Promoted by Chiral Aziridine-Phosphines". Catalysts 12, nr 4 (31.03.2022): 394. http://dx.doi.org/10.3390/catal12040394.
Pełny tekst źródłaFeringa, Ben L., i Richard A. van Delden. "Absolute Asymmetric Synthesis: The Origin, Control, and Amplification of Chirality". Angewandte Chemie International Edition 38, nr 23 (7.12.1999): 3418–38. http://dx.doi.org/10.1002/(sici)1521-3773(19991203)38:23<3418::aid-anie3418>3.0.co;2-v.
Pełny tekst źródłaBarron, L. D. "True and false chirality and absolute asymmetric synthesis". Journal of the American Chemical Society 108, nr 18 (wrzesień 1986): 5539–42. http://dx.doi.org/10.1021/ja00278a029.
Pełny tekst źródłaYamamoto, Satoshi, Kenji Matsuda i Masahiro Irie. "Absolute Asymmetric Photocyclization of a Photochromic Diarylethene Derivative in Single Crystals". Angewandte Chemie International Edition 42, nr 14 (11.04.2003): 1636–39. http://dx.doi.org/10.1002/anie.200250417.
Pełny tekst źródłaKuhn, Alexander, i Peer Fischer. "Absolute Asymmetric Reduction Based on the Relative Orientation of Achiral Reactants". Angewandte Chemie International Edition 48, nr 37 (1.09.2009): 6857–60. http://dx.doi.org/10.1002/anie.200902841.
Pełny tekst źródłaWu, Yusheng, Lothar Esser i Jef K. De Brabander. "Revision of the Absolute Configuration of Salicylihalamide A through Asymmetric Total Synthesis". Angewandte Chemie 39, nr 23 (1.12.2000): 4308–10. http://dx.doi.org/10.1002/1521-3773(20001201)39:23<4308::aid-anie4308>3.0.co;2-4.
Pełny tekst źródłaBielski, Roman, i Michal Tencer. "Macroscopically chiral system of three independent orientational effects as a condition for absolute asymmetric synthesis". Canadian Journal of Chemistry 81, nr 9 (1.09.2003): 1029–37. http://dx.doi.org/10.1139/v03-128.
Pełny tekst źródłaKaimori, Yoshiyasu, Yui Hiyoshi, Tsuneomi Kawasaki, Arimasa Matsumoto i Kenso Soai. "Formation of enantioenriched alkanol with stochastic distribution of enantiomers in the absolute asymmetric synthesis under heterogeneous solid–vapor phase conditions". Chemical Communications 55, nr 36 (2019): 5223–26. http://dx.doi.org/10.1039/c9cc01875a.
Pełny tekst źródłaRozprawy doktorskie na temat "Absolute asymmetric catalysis"
Sallembien, Quentin. "Controlling handedness of triarylamine trisamide assemblies by means of circularly polarized light or chiral additives". Electronic Thesis or Diss., Sorbonne université, 2021. http://www.theses.fr/2021SORUS499.
Pełny tekst źródłaTo pave the way for the absolute asymmetric catalysis, triarylamine trisamide (TATA) supramolecular helical polymers were investigated under the influence of circularly polarized light (CPL) and chiral additives/solvents. The association properties of TATA molecules with saturated or diacetylenic side chains were probed in presence and absence of CPL, by SANS, UV–Vis–NIR, FT–IR, NMR and EPR. The two types of self-assembly formed by these TATA molecules, non-specific aggregates and hydrogen-bonded helical stacks, are in competition and the majority assembly depends on conditions (concentration, temperature, solution/gel/solid). Light and the resulting radical cationic species do not strongly affect the structure of these assemblies, while the co-assembly between neutral and radical cationic species is demonstrated. In these co-assemblies, the unpaired electrons are either slowly delocalized in solution, because of the disorder in assemblies, or rapidly delocalized within long aligned fibers of thin films. Our CD study discards the possibility of using CPL to direct the handedness of TATA-SDA assemblies in the conditions stated in the literature. Finally, the synthesis of TATA ligands bearing a triphenylphosphine unit was achieved. Their study in toluene, dichloromethane and decalin showed the thermoreversible formation of long hydrogen-bonded stacks. Despite the use of a library of enantiopure small molecules as chiral additives or solvents, no biased supramolecular helices were detected. The in-depth characterization of assemblies carried out in this thesis paves the way towards a better control of the structure of functionalized helical assemblies
Gruner, Konstanze K., Thomas Hopfmann, Kazuhiro Matsumoto, Anne Jäger, Tsutomu Katsuki i Hans-Joachim Knölker. "Efficient iron-mediated approach to pyrano[3,2-a]carbazole alkaloids - first total syntheses of O-methylmurrayamine A and 7-methoxymurrayacine, first asymmetric synthesis and assignment of the absolute configuration of (−)-trans-dihydroxygirinimbine". Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-138748.
Pełny tekst źródłaDieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich
Gruner, Konstanze K., Thomas Hopfmann, Kazuhiro Matsumoto, Anne Jäger, Tsutomu Katsuki i Hans-Joachim Knölker. "Efficient iron-mediated approach to pyrano[3,2-a]carbazole alkaloids - first total syntheses of O-methylmurrayamine A and 7-methoxymurrayacine, first asymmetric synthesis and assignment of the absolute configuration of (−)-trans-dihydroxygirinimbine". Royal Society of Chemistry, 2011. https://tud.qucosa.de/id/qucosa%3A27777.
Pełny tekst źródłaDieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
Części książek na temat "Absolute asymmetric catalysis"
Taber, Douglass F. "The Li Synthesis of (–)-Fusarisetin A". W Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0097.
Pełny tekst źródłaTaber, Douglass F. "C–H Functionalization: The Maimone Synthesis of Podophyllotoxin". W Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0021.
Pełny tekst źródła"α-Substitution in Carbonyl Compounds and Derivatives". W The Chemistry of Carbonyl Compounds and Derivatives, 201–73. The Royal Society of Chemistry, 2022. http://dx.doi.org/10.1039/9781837670888-00201.
Pełny tekst źródłaTaber, Douglass. "Stereocontrolled Construction of C-N Rings: The Vanderwal Synthesis of Norfluorocurarine". W Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0056.
Pełny tekst źródłaTaber, Douglass F. "Synthesis of Naturally Occurring Cyclic Ethers: Boivivianin B (Murakami), SC- Δ 13 -9-IsoF (Taber), Brevisamide (Panek, Lindsley,Ghosh), Gambierol (Mori)". W Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0050.
Pełny tekst źródłaTaber, Douglass F. "C–O Ring Construction: Sauropus Hexoside (Xie/Wu), (+)-Ipomeamarone (Usuki), Decytospolide A (Fujioka), Cytospolide P (Goswami), (+)-Didemniserinolipid B (Tong), Gymnothelignan N (She)". W Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0051.
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