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Artykuły w czasopismach na temat "Indoles"
Sharma, Upendra, Inder Kumar i Rakesh Kumar. "Recent Advances in the Regioselective Synthesis of Indoles via C–H Activation/Functionalization". Synthesis 50, nr 14 (28.05.2018): 2655–77. http://dx.doi.org/10.1055/s-0037-1609733.
Pełny tekst źródłaVincent, Guillaume, Hussein Abou-Hamdan i Cyrille Kouklovsky. "Dearomatization Reactions of Indoles to Access 3D Indoline Structures". Synlett 31, nr 18 (24.06.2020): 1775–88. http://dx.doi.org/10.1055/s-0040-1707152.
Pełny tekst źródłaKumar, Anil, i Ganesh Shelke. "Sc(OTf)3-Catalyzed Oligomerization of Indole: One-Pot Synthesis of 2-[2,2-Bis(indol-3-yl)ethyl]anilines and 3-(Indolin-2-yl)indoles". Synthesis 49, nr 18 (1.08.2017): 4321–26. http://dx.doi.org/10.1055/s-0036-1588181.
Pełny tekst źródłaTrubitsõn, Dmitri, i Tõnis Kanger. "Enantioselective Catalytic Synthesis of N-alkylated Indoles". Symmetry 12, nr 7 (17.07.2020): 1184. http://dx.doi.org/10.3390/sym12071184.
Pełny tekst źródłaFang, Xinxin, Shang Gao, Zijun Wu, Hequan Yao i Aijun Lin. "Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones". Organic Chemistry Frontiers 4, nr 2 (2017): 292–96. http://dx.doi.org/10.1039/c6qo00698a.
Pełny tekst źródłaLi, Jiao, i Chun-Lin Zhuang. "Natural Indole Alkaloids from Marine Fungi: Chemical Diversity and Biological Activities". Pharmaceutical Fronts 03, nr 04 (grudzień 2021): e139-e163. http://dx.doi.org/10.1055/s-0041-1740050.
Pełny tekst źródłaAshram, Muhammad, Ahmed Al-Mustafa, Wael A. Al-Zereini, Firas F. Awwadi i Islam Ashram. "A convenient one-pot approach to the synthesis of novel pyrazino[1,2-a]indoles fused to heterocyclic systems and evaluation of their biological activity as acetylcholinesterase inhibitors". Zeitschrift für Naturforschung B 76, nr 5 (1.05.2021): 303–12. http://dx.doi.org/10.1515/znb-2020-0205.
Pełny tekst źródłaYan, Jianwei, Guangjie He, Fulin Yan, Jixia Zhang i Guisheng Zhang. "The dicarbonylation of indoles via Friedel–Crafts reaction with dicarbonyl nitrile generated in situ and retro-cyanohydrination". RSC Advances 6, nr 50 (2016): 44029–33. http://dx.doi.org/10.1039/c6ra04016k.
Pełny tekst źródłaSharapov, Ainur D., Ramil F. Fatykhov, Igor A. Khalymbadzha, Maria I. Valieva, Igor L. Nikonov, Olga S. Taniya, Dmitry S. Kopchuk i in. "Fluorescent Pyranoindole Congeners: Synthesis and Photophysical Properties of Pyrano[3,2-f], [2,3-g], [2,3-f], and [2,3-e]Indoles". Molecules 27, nr 24 (13.12.2022): 8867. http://dx.doi.org/10.3390/molecules27248867.
Pełny tekst źródłaHazra, Somjit, Biplab Mondal, Rajendra Narayan De i Brindaban Roy. "Pd-catalyzed dehydrogenative C–H activation of iminyl hydrogen with the indole C3–H and C2–H bond: an elegant synthesis of indeno[1,2-b]indoles and indolo[1,2-a]indoles". RSC Advances 5, nr 29 (2015): 22480–89. http://dx.doi.org/10.1039/c4ra16661b.
Pełny tekst źródłaRozprawy doktorskie na temat "Indoles"
Scott, Karen Ann. "Synthetic studies related to the synthesis of vincristine". Thesis, University of Strathclyde, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367067.
Pełny tekst źródłaMartin, Tracey. "Claisen rearragements in indoles". Thesis, Imperial College London, 1986. http://hdl.handle.net/10044/1/38097.
Pełny tekst źródłaStempel, Erik [Verfasser]. "Construction of cyclohepta[b]indoles in the total synthesis of indole alkaloids / Erik Stempel". Hannover : Technische Informationsbibliothek (TIB), 2017. http://d-nb.info/1137165995/34.
Pełny tekst źródłaKeech, Peter George. "Electrochemical oxidation of simple indoles". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ61917.pdf.
Pełny tekst źródłaMascal, Mark James. "Synthesis of 3,4-bridged indoles". Thesis, Imperial College London, 1989. http://hdl.handle.net/10044/1/47561.
Pełny tekst źródłaJennings, Peter. "Photophysical study of electropolymerised indoles". Thesis, University of Edinburgh, 1999. http://hdl.handle.net/1842/12295.
Pełny tekst źródłaHarrison, Carrie-Ann. "Synthetic approaches to tremorgenic indoles". Thesis, Loughborough University, 1994. https://dspace.lboro.ac.uk/2134/32532.
Pełny tekst źródłaEl, Marrouki Dalel. "Contribution à l’étude de la réactivité de quelques accepteurs de Michael cycliques et applications". Electronic Thesis or Diss., Université de Lorraine, 2020. http://www.theses.fr/2020LORR0197.
Pełny tekst źródłaThis thesis focuses on the synthesis of some nitrogenous heterocycles from the same family of precursors: 1,4-diketones. These 1,4-diketones have been obtained either by a Nef reaction through the conversion of nitro compounds into ketones or by a Wittig reaction using various Wittig ylides and cyclohexanedione. These reaction intermediates were subsequently used for the synthesis of indole derivatives via a 1,2-addition reaction. We were also able to turn the selectivity of the reaction towards the synthesis of indolones from a 1,4-addition reaction. With hydrazine monohydrate, 1,4-diketones have also provided access to cinnolines in excellent yields
Hammoud, Sokaina. "Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation". Thesis, Tours, 2015. http://www.theses.fr/2015TOUR4034.
Pełny tekst źródłaA new access pathway to the original tricyclic structures "di-iodinated oxazino-indole" was developed from the commercial 1H-indole-2-carboxylic acids or functionalized 1H-indole-2-carboxylic acid obtained by Hemetsberger-Knittel reaction. The last step in this sequence is an iodocyclisation reaction that is proved to be completely regio- and stereoselective via 6-exo-dig process. This methodology was then extended to isoindolic series allowing access to original "di-iodinated oxazino-isoindole" motifs. To further extend this methodology, new"di-iodinated oxazepino-indoles" were prepared using the same synthetic approach from the 1H-indole-7-carboxylic acid. The reactivity of the di-iodinated tri-cyclic structures has been studied via Cross-Coupling reactions (Stille, Sonogashira and Suzuki) by the use of palladium salts allowing a regioselective functionalization of the exocyclic iodine
Westermaier, Martin. "Electrophilic Substitutions of Indoles and Pyrroles:". Diss., lmu, 2007. http://nbn-resolving.de/urn:nbn:de:bvb:19-77431.
Pełny tekst źródłaKsiążki na temat "Indoles"
1927-, Saxton J. Edwin, red. Indoles. Chichester: Wiley, 1994.
Znajdź pełny tekst źródłaservice), SpringerLink (Online, red. Heterocyclic Scaffolds II: Reactions and Applications of Indoles. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2011.
Znajdź pełny tekst źródłaVoro, Tevita N. Synthesis of potentially biologically active indoles and pyrroles. Norwich: Universityof East Anglia, 1990.
Znajdź pełny tekst źródłaMurray, Paul Edward. [ Beta]-nucleophilic substitution in indoles: The synthesis of Chartellamide A. Manchester: University of Manchester, 1994.
Znajdź pełny tekst źródłaBenzies, David W. M. Some aspects of the synthesis and reactions of substituted indoles. Norwich: University of East Anglia, 1989.
Znajdź pełny tekst źródłaservice), SpringerLink (Online, red. Functional Phthalocyanine Molecular Materials. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.
Znajdź pełny tekst źródła1927-, Saxton J. Edwin, red. Monoterpenoid indole alkaloids. Chichester [England]: Wiley, 1994.
Znajdź pełny tekst źródłaGribble, Gordon W. Indole Ring Synthesis. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118695692.
Pełny tekst źródłaRoffey, Maureen. Indoors. Martinez, CA: Discovery Books, 1989.
Znajdź pełny tekst źródłaIndoors. London: Collins Educational, 1992.
Znajdź pełny tekst źródłaCzęści książek na temat "Indoles"
Brown, E. G. "Indoles". W Ring Nitrogen and Key Biomolecules, 192–207. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4906-8_9.
Pełny tekst źródłaLi, Jie Jack, i Minmin Yang. "Indoles". W Drug Discovery with Privileged Building Blocks, 143–51. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003190806-17.
Pełny tekst źródłaBronner, Sarah M., G. Yoon J. Im i Neil K. Garg. "Indoles and Indolizidines". W Heterocycles in Natural Product Synthesis, 221–65. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634880.ch7.
Pełny tekst źródłaMenendez-Pelaez, Armando, i Gerald R. Buzzell. "Harderian Gland Indoles". W Harderian Glands, 219–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76685-5_13.
Pełny tekst źródłaJoule, J. A., K. Mills i G. F. Smith. "Indoles: reactions and synthesis". W Heterocyclic Chemistry, 305–49. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_17.
Pełny tekst źródłaJuwarker, Hemraj, Jae-min Suk i Kyu-Sung Jeong. "Indoles and Related Heterocycles". W Topics in Heterocyclic Chemistry, 177–204. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/7081_2010_31.
Pełny tekst źródłaWeedon, Alan. "The Photochemistry of Indoles". W Advances in Photochemistry, 229–77. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470133538.ch4.
Pełny tekst źródłaMuzalevskiy, Vasiliy M., Olga V. Serdyuk i Valentine G. Nenajdenko. "Chemistry of Fluorinated Indoles". W Fluorine in Heterocyclic Chemistry Volume 1, 117–56. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04346-3_3.
Pełny tekst źródłaSundberg, Richard J. "Electrophilic Substitution Reactions of Indoles". W Topics in Heterocyclic Chemistry, 47–115. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/7081_2010_52.
Pełny tekst źródłaSmith, Lowell R. "Alkyl, Alkenyl and Alkynyl Indoles". W Chemistry of Heterocyclic Compounds: A Series Of Monographs, 65–126. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186930.ch2.
Pełny tekst źródłaStreszczenia konferencji na temat "Indoles"
Wipf, Peter, i Filip Petronijevic. "New Approaches to Indoles and Indole Alkaloids". W 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0388-1.
Pełny tekst źródłaSchauerte, Joseph A., i Ari Gafni. "Time Resolved Fluorescence Of Substituted Indoles". W OE/LASE '89, redaktorzy Robert R. Birge i Henry H. Mantsch. SPIE, 1989. http://dx.doi.org/10.1117/12.951649.
Pełny tekst źródłaDemchenko, Alexander P., Jacques Gallay i Michel Vincent. "Photophysics of indoles in polar environments". W Laser Applications in Life Sciences: 5th International Conference, redaktorzy Pavel A. Apanasevich, Nikolai I. Koroteev, Sergei G. Kruglik i Victor N. Zadkov. SPIE, 1995. http://dx.doi.org/10.1117/12.197412.
Pełny tekst źródłaFeu, Karla S., Anna M. Deobald, Arlene G. Corrêa i Marcio W. Paixão. "Tandem Organocatalytic Functionalization and Fisher Indole Synthesis: A Greener Approach for the Synthesis of Indoles". W 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0342-1.
Pełny tekst źródłaSeijas, Julio, M. Vázquez-Tato, José Crecente-Campo, M. Gómez-Doval i Lorena Núñez-Álvarez. "Microwave assisted synthesis of indoles: Madelung's Reaction". W The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01258.
Pełny tekst źródłaCiprian-Ollivier, J., i M. G. Cetkovich-Bakmas. "METHYLATED INDOLES IN OBSESSIVE-COMPULSIVE AND PHOBIC DISORDERS". W IX World Congress of Psychiatry. WORLD SCIENTIFIC, 1994. http://dx.doi.org/10.1142/9789814440912_0009.
Pełny tekst źródłaWestbrook, John D., Ronald M. Levy i Karsten Krogh-Jespersen. "Simulation of photophysical processes of indoles in solution". W OE/LASE '92, redaktor Joseph R. Lakowicz. SPIE, 1992. http://dx.doi.org/10.1117/12.58196.
Pełny tekst źródłaBagnoli, Luana, Katja Berettoni, Francesca Marini i Claudio Santi. "An efficient cascade reaction for the synthesis of oxazino[4,3-a]indoles and pyrano[3,4-b]indoles from vinyl selenones". W The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a037.
Pełny tekst źródłaMuino, Pedro L., i Patrik R. Callis. "Simulations of solvent effects on fluorescence spectra and dynamics of indoles". W OE/LASE '94, redaktor Joseph R. Lakowicz. SPIE, 1994. http://dx.doi.org/10.1117/12.182745.
Pełny tekst źródłaLapa, G., i O. Tolkachev. "A Novel Approach to the Synthesis of Substututed Indoles via Nitrilic Condensation." W The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01748.
Pełny tekst źródłaRaporty organizacyjne na temat "Indoles"
Bjeldanes, Leonard. Control of Breast Tumor Cell Growth by Dietary Indoles. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1998. http://dx.doi.org/10.21236/adb240497.
Pełny tekst źródłaChamovitz, A. Daniel, i Georg Jander. Genetic and biochemical analysis of glucosinolate breakdown: The effects of indole-3-carbinol on plant physiology and development. United States Department of Agriculture, styczeń 2012. http://dx.doi.org/10.32747/2012.7597917.bard.
Pełny tekst źródłaLuo, Jun. Molecular Characterization of Indolent Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, październik 2014. http://dx.doi.org/10.21236/ada613287.
Pełny tekst źródłaLuo, Jun. Molecular Characterization of Indolent Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, październik 2013. http://dx.doi.org/10.21236/ada590674.
Pełny tekst źródłaJerry D. Cohen. Metabolic regulation of the plant hormone indole-3-acetic acid. Office of Scientific and Technical Information (OSTI), listopad 2009. http://dx.doi.org/10.2172/966706.
Pełny tekst źródłaCohen, Jerry D., Ephraim Epstein, Mark Roh i Joseph Riov. Indole-3-Acetic Acid Metabolism in Relation to Root Initiation. United States Department of Agriculture, październik 1985. http://dx.doi.org/10.32747/1985.7566592.bard.
Pełny tekst źródłaFricker, Jon, Menna Noureldin, Timothy Stroshine i Wayne Richardson. Cost‐Effective Data Collection to Support INDOT’s Mission. Purdue University, grudzień 2012. http://dx.doi.org/10.5703/1288284315040.
Pełny tekst źródłaKe, Yue, Lisa Lorena Losada-Rojas, Davis Chacon-Hurtado, Konstantina Gkritza i Jon D. Fricker. Incorporating Economic Resilience Metrics into INDOT’s Transportation Decision-Making. Purdue University, 2020. http://dx.doi.org/10.5703/1288284317115.
Pełny tekst źródłaArboleda, Carlos, Hyung Jeong i Dulcy Abraham. Evaluation, Analysis, and Enhancement of INDOT's Utility Accommodation Policy. West Lafayette, IN: Purdue University, 2004. http://dx.doi.org/10.5703/1288284313220.
Pełny tekst źródłaAdsit, Sarah E., Theodora Konstantinou, Konstantina Gkritza i Jon D. Fricker. Public Acceptance of INDOT’s Traffic Engineering Treatments and Services. Purdue University, 2021. http://dx.doi.org/10.5703/1288284317280.
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