Thematische Bibliographien / N - Aryl Y - Lactam

Inhaltsverzeichnis

  1. Zeitschriftenartikel
  2. Dissertationen
  3. Bücher
  4. Buchteile
  5. Konferenzberichte

Auswahl der wissenschaftlichen Literatur zum Thema „N - Aryl Y - Lactam“

Autor: Grafiati
Veröffentlicht am 18. Mai 2024

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Machen Sie sich mit den Listen der aktuellen Artikel, Bücher, Dissertationen, Berichten und anderer wissenschaftlichen Quellen zum Thema "N - Aryl Y - Lactam" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Zeitschriftenartikel zum Thema "N - Aryl Y - Lactam"

1

Tsang, Wing Y., Naveed Ahmed, Karl Hemming und Michael I. Page. „Competitive endo- and exo-cyclic C–N fission in the hydrolysis of N-aroyl β-lactams“. Canadian Journal of Chemistry 83, Nr. 9 (01.09.2005): 1432–39. http://dx.doi.org/10.1139/v05-153.

Der volle Inhalt der Quelle
Annotation:
The balance between endo- and exo-cyclic C–N fission in the hydrolysis of N-aroyl β-lactams shows that the difference in reactivity between strained β-lactams and their acyclic analogues is minimal. Attack of hydroxide ion occurs preferentially at the exocyclic acyl centre rather than that of the β-lactam during the hydrolysis of N-p-nitrobenzoyl β-lactam. In general, both endo- and exo-cyclic C–N bond fission occurs in the alkaline hydrolysis of N-aroyl β-lactams, the ratio of which varies with the aryl substituent. Hence, the Brønsted β-values differ for the two processes: –0.55 for the ring-opening reaction and –1.54 for the exocyclic C–N bond fission reaction. For the pH-independent and acid-catalysed hydrolysis of N-benzoyl β-lactam, less than 3% of products are derived from exocyclic C–N bond fission. Key words: β-lactams, hydrolysis, linear free energy relationships, strain.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
2

Barba, Victor, Cecilia Hernández, Susana Rojas-Lima, Norberto Farfán und Rosa Santillan. „Preparation of N-aryl-substituted spiro-β-lactams via Staudinger cycloaddition“. Canadian Journal of Chemistry 77, Nr. 12 (05.12.1999): 2025–32. http://dx.doi.org/10.1139/v99-212.

Der volle Inhalt der Quelle
Annotation:
The interest in the study of β-lactams continues due to their therapeutic importance as antibiotics. In this work, six spiro-β-lactams (7a-7c, 8a-8c) have been prepared using the [2+2] cycloaddition of isomaleimides to acid chlorides. The heterobicyclic structures obtained have been characterized by mass spectrometry, IR, NMR spectroscopy, and for compounds 7a, 7b, and 8b the X-ray crystallographic study showed a nearly planar arrangement for the β-lactam ring.Key words: β-lactams, azetidinone, isomaleimides, ketenes, X-ray crystallography.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
3

Möhrle, H., und M. Jeandrée. „Chinazolinderivate durch Cyclodehydrierung von N-(2-substituierten Aryl)-Piperidinen / Quinazoline Derivatives by Cyclodehydrogenation of N-(2-Substituted Aryl)-Piperidines“. Zeitschrift für Naturforschung B 54, Nr. 12 (01.12.1999): 1577–88. http://dx.doi.org/10.1515/znb-1999-1217.

Der volle Inhalt der Quelle
Annotation:
Dehydrogenation of the N-[2-(aminocarbonyl)phenyl]piperidines 1 -5 using Hg(II)-EDTA, generated the quinazolinones 6 -9 . Increasing size of the 4-substituent in the piperidine decreased the oxidation rate and the product yield.N-[2-(Hydroxyiminomethyl)phenyl]piperidines 18-22 showed a different behaviour. While 18 with H g(II)-EDTA in water produced the oxime lactam 24 in quantitative yield, the 4- substituted piperidines 19-21 caused not only a lower reaction rate but also an altered product pattern. The double dehydrogenation to lactams was reduced and the cyclic nitrones, formed by two electron withdrawal, became dominant. From the spiro compounds 21 and 22, solely the quinazoline-N-oxides 29 and 30 resulted. The mechanism of the reactions is discussed.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
4

Fang, Zeguo, Lin Xie, Liang Wang, Qian Zhang und Dong Li. „Silver-catalyzed cascade cyclization and functionalization of N-aryl-4-pentenamides: an efficient route to γ-lactam-substituted quinone derivatives“. RSC Advances 12, Nr. 41 (2022): 26776–80. http://dx.doi.org/10.1039/d2ra05283k.

Der volle Inhalt der Quelle
Annotation:
The synthesis of γ-lactam and related 2-oxazolidinone substituted quinone derivatives through a Ag2O-catalyzed cascade cyclization and functionalization of N-ary-4-pentenamides and N-aryl allyl carbamates has been developed.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
5

Saliu, Francesco, Marco Orlandi und Maurizio Bruschi. „N-Aryl Lactams by Regioselective Ozonation of N-Aryl Cyclic Amines“. ISRN Organic Chemistry 2012 (15.10.2012): 1–5. http://dx.doi.org/10.5402/2012/281642.

Der volle Inhalt der Quelle
Annotation:
Ozonation of N-aryl-cyclic amines in organic solvents gave N-aryl-lactams regioselectively. In particular, 4-(4-aminophenyl)-morpolin-3-one, a key intermediate in the preparation of factor Xa inhibitors, was obtained in fair yields. The method represents an alternative approach for the lactamization of tertiary N-arylic substrates and is based on a “metal-free” introduction of the carbonyl function into the heterocyclic ring.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
6

Haldar, Pranab, und Jayanta K. Ray. „CAN mediated decarboxylative hydroxylation/alkoxylation of N-aryl-γ-lactam-carboxylic acids at room temperature: an easy access to N-aryl-α-hydroxy/alkoxy-γ-lactams“. Tetrahedron Letters 49, Nr. 22 (Mai 2008): 3659–62. http://dx.doi.org/10.1016/j.tetlet.2008.03.147.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
7

Yurino, Taiga, Takeshi Ohkuma, Hamdiye Ece und Yuji Tange. „Silyl Cyanopalladate-Catalyzed Friedel–Crafts-Type Cyclization Affording 3-Aryloxindole Derivatives“. Synlett 32, Nr. 09 (26.01.2021): 935–39. http://dx.doi.org/10.1055/a-1373-7017.

Der volle Inhalt der Quelle
Annotation:
Abstract3-Aryloxindole derivatives were synthesized through a Friedel–Crafts-type cyclization. The reaction was catalyzed by a trimethylsilyl tricyanopalladate complex generated in situ from trimethylsilyl cyanide and Pd(OAc)2. Wide varieties of diethyl phosphates derived from N-arylmandelamides were converted almost quantitatively into oxindoles. When N,N-dibenzylamide was used instead of an anilide substrate, a benzo-fused δ-lactam was obtained. An oxindole product was subjected to substitution reactions to afford 3,3-diaryloxindoles with two different aryl groups.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
8

Patra, Prasanta, Gandhi K. Kar, Aparna Sarkar, Jayanta K. Ray, Tista Dasgupta, Mahua Ghosh und Sugata Bhattacharya. „N-Aryl Modification in γ-Lactam: Design and Synthesis of Novel Monocyclic γ-Lactam Derivatives as Inhibitor for Bacterial Propagation“. Synthetic Communications 42, Nr. 20 (21.06.2012): 3031–41. http://dx.doi.org/10.1080/00397911.2011.574807.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
9

Dorbec, Matthieu, Jean-Claude Florent, Claude Monneret, Marie-Noëlle Rager und Emmanuel Bertounesque. „1-Aryltetralin privileged structure-based libraries: parallel synthesis of N-aryl and N-biaryl γ-lactam lignans“. Tetrahedron 62, Nr. 50 (Dezember 2006): 11766–81. http://dx.doi.org/10.1016/j.tet.2006.09.026.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
10

Patra, Prasanta, Gandhi K. Kar, Aparna Sarkar, Jayanta K. Ray, Tista Dasgupta, Mahua Ghosh und Sugata Bhattacharya. „ChemInform Abstract: N-Aryl Modification in γ-Lactam: Design and Synthesis of Novel Monocyclic γ-Lactam Derivatives as Inhibitor for Bacterial Propagation.“ ChemInform 44, Nr. 1 (01.01.2013): no. http://dx.doi.org/10.1002/chin.201301160.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
Mehr Quellen

Dissertationen zum Thema "N - Aryl Y - Lactam"

1

Barman, Gopa. „Synthetic studies on N - Aryl Y - Lactam & N - Aryl Y - Thio - Lactam : chemoselective Transformation to N-Aryl-Pyrrolidine, N-Aryl Succinimide and Other Bioactive Compounds“. Thesis, University of North Bengal, 2009. http://hdl.handle.net/123456789/1379.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
2

Bhattacharya, Biplob. „Synthesis and Anti-MRSA Activity of Hydrophilic C3-Acylated N-Thiolated β-Lactams and N-Acyl Ciprofloxacin-N-Thiolated β-Lactam Hybrids“. Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4289.

Der volle Inhalt der Quelle
Annotation:
The Turos laboratory has been working with N-thiolated β-lactams for years trying to understand the mode of action and structural features it needs to have biological activity. Over the years new data has shown promising inhibitory activity against various microbes. In this dissertation, a review of the vast amount of work carried out on N-thiolated β-lactams in Turos laboratory has been done and their novelty, in terms of structure and mechanism has been discussed. A complete outline of our work in the discovery and ongoing development of these compounds, starting from our initial, unexpected finding of antimicrobial activity for one of the lead compounds, to a more complete understanding of their chemical and biological mode of action and potential utility as antibacterial compounds, has been provided. Previous researches by graduate students in the Turos laboratory have shown that N-thiolated β-lactams targets Type II Fatty Acid Synthesis (FAS). In process of understanding this further, other FAS inhibiting antibiotics like Triclosan were compared to our lactams by adding excess of exogenous fatty acids. Results revealed vast differences in the MIC value of triclosan and N-thiolated β-lactams, giving an idea that there might be a different mode of action or a different target altogether. The third chapter discusses the study of attaching hydrophilic C3 side chains like amino acids and carbohydrates on N-thiolated β-lactams while studying the influence of microbiological activity. From the study it was found that the lengthening of the side chain halts the inhibitory activity regardless of whether the side chain contains unsaturation or branching. Results showed that polar groups were not well tolerated and the inhibitory activity goes down regardless of polarity. Finally, research on dual-action antibiotics was discussed. Antibiotics cause continuous bacterial resistance and in this aspect use of two drugs with different mode of action can call for reduction of the resistance. Herein, N-acyl ciprofloxacin and N-thiolated β-lactams were connected together via an ester linkage. Six new hybrid compounds have been synthesized successfully and tested against E. faecium, K. pneumoniae, A. baumannii, P. aeruginosa, and E. cloacae.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
3

Bekdemir, Yunus. „The mechanisms of hydrolysis and protonation behaviour of N-aryl sultams“. Thesis, University of Essex, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387004.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
4

Dyke, Alan. „Novel Câ‚‚-symmetric N,N-donor ligands and the anionic thia-Fries rearrangement of aryl triflates“. Thesis, University of Bristol, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.404435.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
5

Yasui, Hiroto. „Studies on Addition to 1-Aryl-1-alkynes and N-Alkynyl Amides“. 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/57271.

Der volle Inhalt der Quelle
Annotation:
Kyoto University (京都大学)
0048
新制・課程博士
博士(工学)
甲第13827号
工博第2931号
新制||工||1433(附属図書館)
26043
UT51-2008-C743
京都大学大学院工学研究科材料化学専攻
(主査)教授 大嶌 幸一郎, 教授 檜山 爲次郎, 教授 松原 誠二郎
学位規則第4条第1項該当
APA, Harvard, Vancouver, ISO und andere Zitierweisen
6

Mori, Shigeki. „Studies on metallation of meso-aryl substituted hexaphyrins and N-fused pentaphyrins“. 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/136922.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
7

Baeza, Mario Ivan. „Synthesis and characterization of acetylenic derivatives of the actinide extractant (aryl)-N,N-di-(alkyl)carbamoylmethylphosphine oxide (CMPO)“. To access this resource online via ProQuest Dissertations and Theses @ UTEP, 2008. http://0-proquest.umi.com.lib.utep.edu/login?COPT=REJTPTU0YmImSU5UPTAmVkVSPTI=&clientId=2515.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
8

Prosen, Katherine Rose. „Investigating the Mode of Action of a Novel N-sec-butylthiolated Beta-lactam Against Staphylococcus aureus“. Scholar Commons, 2010. http://scholarcommons.usf.edu/etd/3609.

Der volle Inhalt der Quelle
Annotation:
N-sec -butylthioloated β-lactam (NsβL) is a novel beta-lactam antimicrobial with a mechanism of action proposed to inhibit 3-oxoacyl-acyl carrier protein synthase (ACP) III (FabH), resulting in the inhibition of fatty acid synthesis. It has been suggested that NsβL inhibits FabH indirectly by inactivating coenzyme-A (CoA). CoA is an essential cofactor for numerous proteins involved in glycolysis, the citric acid cycle (TCA), and pyruvate metabolism, in addition to fatty acid biosynthesis. This study aimed to determine the effects of NsβL on a diverse array of laboratory and clinical Staphylococcus aureus isolates by analyzing the mode of resistance in spontaneous and adaptive mutant NsβL-resistant mutants. Phenotypic analysis of the mutants was performed, as well as sequence analysis of fabH; along with comparative proteomic analysis of intracellular proteomes. Our results indicate that NsβL resistance is mediated by drastic changes in the cell wall, oxidative stress response, virulence regulation, and those pathways associated with CoA. It is our conclusion that Nsβ L has activity towards CoA, resulting in wide-spread effects on metabolism, virulence factor production, stress response, and antimicrobial resistance.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
9

Cui, Xiuhua. „Asymmetric hydrogenations of aryl alkenes using imidazol-2-ylidene iridium complexes“. Texas A&M University, 2005. http://hdl.handle.net/1969.1/2456.

Der volle Inhalt der Quelle
Annotation:
A library of iridium complexes featuring oxazoline and imidazol-2-ylidene ligands were synthesized by reaction of a library of imidazoles with a second library of oxazoline iodides. These complexes were active catalysts for hydrogenations of aryl substituted monoenes. Tri- and 1,1-disubstituted alkenes were hydrogenated quantitatively with ee??s up to 99% at 1 atm hydrogen pressure. Catalyst, substrate, temperature and pressure effects were studied. The iridium complexes were also used for the kinetic study of hydrogenation of 2,3- diphenylbutadiene. This hydrogenation is a stepwise reaction: one double bond was hydrogenated first, then the second one. Both step hydrogenations were zero order in alkene. The consumption of 2,3-diphenylbutadiene was first order in catalyst, and probably first order in hydrogen pressure too. The enantioselectivity for the first step hydrogenation was low. There were match and mismatch catalyst-substrate relationships for the second step hydrogenation, and the enantioselectivities for this step were catalyst controlled. NMR studies indicated that the initiation of the reaction involved both hydrogen and alkene substrate. A competitive experiment was designed to explore the formation of meso-alkane at first step hydrogenation, and the results indicated that the alkane was formed predominantly via an associative mechanism. Four types of conjugate dienes were synthesized and hydrogenated. Different reactivities and selectivities were obtained for each type of dienes. In the best case, a diene was hydrogenated quantitatively with an excellent ent/meso ratio of 20:1.0 and 99% enantioselectivity. The scope, limitation and potential applications of the reactions were discussed. A selection of the dienes was hydrogenated with the Crabtree??s catalyst, for comparison, and the yields, conversions and diastereoselectivities were inferior to those from iridium-oxazoline-imidazol-2-ylidene catalysts.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
10

Jiao, Dezhi. „Alkyl and aryl imidazolium salts in aqueous supramolecular systems with cucurbit[n]uril“. Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610692.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
Mehr Quellen

Bücher zum Thema "N - Aryl Y - Lactam"

1

Henderson, Colin M. Nucleophilic additions to C-aryl, N-arylsulphonyl methyleneimines. [S.l: The Author], 1992.

Den vollen Inhalt der Quelle finden
APA, Harvard, Vancouver, ISO und andere Zitierweisen
2

Ikhlef, Fatima. Routes to 4-aryl-1-N-methylanilinobut-3-en-2-ones and reactions of 2-phenylethylamine. Salford: University of Salford, 1985.

Den vollen Inhalt der Quelle finden
APA, Harvard, Vancouver, ISO und andere Zitierweisen
3

International Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds (3rd 1987 Dearborn, Mich.). Carcinogenic and mutagenic responses to aromatic amines and nitroarenes: Proceedings of the Third International Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds, held April 25-28, 1987, in Dearborn Michigan. Herausgegeben von King Charles M. 1932-, Romano Louis James 1950- und Schuetzle Dennis 1942-. New York: Elsevier, 1988.

Den vollen Inhalt der Quelle finden
APA, Harvard, Vancouver, ISO und andere Zitierweisen
4

Carcinogenic and mutagenic N-substituted aryl compounds. [Research Triangle Park, NC]: National Institutes of Health, National Institute of Environmental Health Sciences, 1994.

Den vollen Inhalt der Quelle finden
APA, Harvard, Vancouver, ISO und andere Zitierweisen
5

Lagerman, Robert K. Metal ion induced decomposition of N-Aryl-O-pivaloylhydroxylamines in aqueous solution. 1989.

Den vollen Inhalt der Quelle finden
APA, Harvard, Vancouver, ISO und andere Zitierweisen

Buchteile zum Thema "N - Aryl Y - Lactam"

1

Atwood, David A. „(IV) into N-C (Aryl) Bonds“. In Inorganic Reactions and Methods, 160. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch145.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
2

Mitchell, Glynn, Nigel J. Barnes, John M. Cox, Ian R. Matthews, David R. Parry, David P. J. Pearson und Stephen C. Smith. „Synthesis and Structure-Activity Relationships in a Novel Class ofN-Aryl Lactam Herbicides“. In ACS Symposium Series, 18–29. Washington, DC: American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2002-0800.ch003.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
3

Monnier, Florian, und Marc Taillefer. „Copper-Catalyzed C(aryl)–N Bond Formation“. In Amination and Formation of sp2 C-N Bonds, 173–204. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/3418_2013_69.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
4

Kawada, Kosuke. „N-Fluoropyridinium Salt Fluorination for Preparing Aryl Fluorides“. In Fluorination, 1–14. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-1855-8_40-1.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
5

Kawada, Kosuke. „N-Fluoropyridinium Salt Fluorination for Preparing Aryl Fluorides“. In Fluorination, 1–14. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-10-1855-8_40-2.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
6

Kawada, Kosuke. „N-Fluoropyridinium Salt Fluorination for Preparing Aryl Fluorides“. In Fluorination, 324–38. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-10-3896-9_40.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
7

Döpp, D., A. A. Hassan, A. M. Nour-el-Din und A. E. Mourad. „A Novel Reaction of Tetracyanoethylene with N-Aryl-Isoindolines“. In Organic Free Radicals, 41–42. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73963-7_21.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
8

Nielsen, David J., und Kingsley J. Cavell. „Pd-NHC Complexes as Catalysts in Telomerization and Aryl Amination Reactions“. In N-Heterocyclic Carbenes in Synthesis, 73–102. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/9783527609451.ch4.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
9

Juliano, Luiz, Maria Helena S. Cezari und Regina S. H. Carvalho. „Studies on lactam formation during the coupling procedures with N α-carbobenzoxy-N G-tosylarginine“. In Peptides 1992, 247–48. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1470-7_99.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
10

Bartsch, Richard A., David A. Babb und Brian E. Knudsen. „Synthesis and Alkali Metal Cation Complexation of N-Aryl [3.2.2] Cryptands“. In Inclusion Phenomena in Inorganic, Organic, and Organometallic Hosts, 407–11. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3987-5_67.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen

Konferenzberichte zum Thema "N - Aryl Y - Lactam"

1

Liu, Chang, Jing Zhu, Wei Huang, Jin Xu, Changgui Lu und Yiping Cui. „Quadratic nonlinear optical properties of N-aryl stilbazolium dyes“. In Nonlinear Optics: Technologies and Applications. SPIE, 2007. http://dx.doi.org/10.1117/12.757577.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
2

Ścianowski, Jacek, Agata Pacuła und Magdalena Obieziurska. „N-aryl benzisoselenazolones – synthesis, transformations and antioxidant activity“. In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a019.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
3

KOIKE, R., J. MOTOYOSHIYA und H. AOYAMA. „THE HIGH ENERGY KEY INTERMEDIATES IN THE PEROXYOXALATE CHEMILUMINESCENCE OF 2,4,6-TRICHLOROPHENYL N-ARYL-N-TOSYLOXAMATES“. In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0037.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
4

Chaves, Humberto T., Ana M. Lobo, Sundaresan Prabhakar und Henry S. Rzepa. „A theoretical mechanistic investigation of asymmetric aziridination by N-Aryl-O-acylhydroxylamines.“ In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47868.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
5

Pindjakova, Dominika, Lucia Vrablova, Tomas Strharsky, Jiri Kos und Josef Jampilek. „Investigation of Interactions of ortho- and para-N-Aryl-Substituted 2-Trifluoromethylcinnamanilides“. In ECSOC-25. Basel Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11651.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
6

Cieślak, Jacek, Jadwiga Jankowska, Michał Sobkowski, Annika Kers, Inger Kers, Jacek Stawinski und Adam Kraszewski. „The reactions of aryl nucleoside H-phosphonates with O-, N-, and S-nucleophiles“. In XIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199902063.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
7

Ridzuan, M. S. M., M. Z. Jaafar und M. M. Zain. „Quantitative structure-activity relationship (QSAR) modelling of N-aryl derivatives as cholinesterase inhibitors“. In 2012 IEEE Symposium on Humanities, Science and Engineering Research (SHUSER). IEEE, 2012. http://dx.doi.org/10.1109/shuser.2012.6269006.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
8

Gonec, Tomas, Lucia Vrablova, Dominika Pindjakova, Tomas Strharsky, Michal Oravec und Josef Jampilek. „Preparation and Hydro-Lipophilic Properties of Monosubstituted N-Aryl-4-hydroxyquinoline-3-carboxanilides“. In International Electronic Conference on Synthetic Organic Chemistry. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13548.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
9

Keung Chui, Wai, Anton Dolzhenko und Hriday Bera. „Synthesis of N-(3(5)-Aryl-1,2,4-triazol-5(3)-yl)-N'-carbethoxythioureas and Their Tautomerism in DMSO Solution“. In The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00187.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
10

Palermo, Mark G., Rohan Beckwith, Christopher S. Straub, Kara Herlihy, Yiping Shen, Xiaolu Zhang, Matthew Clapham und Brian Hurley. „Abstract C54: Aryl-N-(1H-imidazol-2-yl)-acetamides: Nonpeptidic binders of Bir3 cIAP protein.“ In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Oct 19-23, 2013; Boston, MA. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1535-7163.targ-13-c54.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
Die Auswahlen zum Thema "N - Aryl Y - Lactam" für konkrete Quellenarten können Sie auch interessieren:
Zeitschriftenartikel Dissertationen
Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!

Zur Bibliographie