Relevant bibliographies by topics / (dihydro-2,5)

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic '(dihydro-2,5)'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "(dihydro-2,5)"

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Herberich, Gerhard E., Trixie Wagner, and Hans-W. Marx. "Borole derivatives XXI, 2,5-diphenyl-2,5,-dihydro-1H-boroles; strctures of tert-butyl-2,5,-diphenyl-2,5-dihydro-1H-borole and of bis(tmeda) lithium 2,5-diphenyl-2,5-dihydro-1H-borolediide." Journal of Organometallic Chemistry 502, no. 1-2 (1995): 67–74. http://dx.doi.org/10.1016/0022-328x(95)05818-a.

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Bröring, Martin, Frédérique Brégier, and Christian Kleeberg. "3,4-Diethyl-2,5-dihydro-1H-pyrrole-2,5-dione." Acta Crystallographica Section C Crystal Structure Communications 63, no. 4 (2007): o225—o227. http://dx.doi.org/10.1107/s0108270107006737.

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HERBERICH, G. E., T. WAGNER, and H. W. MARX. "ChemInform Abstract: Borole Derivatives. Part 21. 2,5-Diphenyl-2,5-dihydro-1H-boroles; Structures of tert-Butyl-2,5-diphenyl-2,5-dihydro-1H-borole and of Bis( tmeda)lithium 2,5-Diphenyl-2,5-dihydro-1H-borolediide." ChemInform 27, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199608183.

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Karpyak, Natalya, Galyna Marshalok, Yaroslav Kovalskyi, and Maria Fedevych. "Joint obtaining of 2,5-diethyl-3,4-dihydro-2H-pyran-2-methanol and sodium salt of 2,5-diethyl-3,4-dihydro-2H-pyran-2-carboxylic acid via CanniZZaro reaction." Chemistry & Chemical Technology 3, no. 2 (2009): 91–94. http://dx.doi.org/10.23939/chcht03.02.091.

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Kinetic regularities of joint obtaining of 2,5-diethyl-3,4-dihydro-2H-pyran-2-methanol and sodium salt of 2,5-diethyl-3,4-dihydro-2H-pyran-2-carboxylic acid have been investigated. Optimal synthesis conditions have been established and physico-chemical characteristics of the main products have been determined.
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Dölling, Karin. "Reaction of iodomethyltin(IV) compounds with (2s)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine." Journal of the Serbian Chemical Society 77, no. 7 (2012): 873–77. http://dx.doi.org/10.2298/jsc111215007d.

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Following the Sch?llkopf methodology the reaction of (2S)-2,5- dihydro-3,6-dimethoxy-2-isopropylpyrazine 1 with iodomethyl trimethylstannane gives (2S,5S)-2,5-dihydro-3,6-dimethoxy-5-trimethylstannylmethyl-2- isopropylpyrazine 2 in good yields. The obtained compound was characterized with elemental analysis and multinuclear (1H, 13C and 119Sn) NMR spectroscopy.
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Salbeck, Josef, and Erhard Günther. "Elektrochemische und spektroelektrochemische Untersuchungen neuer S-heterochinoider Elektronenakzeptoren, N-Cyanimin-substituierte Thieno[3,2-b]thiophen-2,5-dione / Electrochemical and Spectroelectrochemical Investigations of New S-Heteroquinoid Electron Acceptors, N-Cyanimine Substituted Thieno[3,2-b]thiophene-2,5-diones." Zeitschrift für Naturforschung B 46, no. 3 (1991): 353–60. http://dx.doi.org/10.1515/znb-1991-0315.

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Huang, Liangzhu, Youqiang Li, Dongmei Gao, and Zhenting Du. "3,4-Bis(4-methoxyphenyl)-2,5-dihydro-1H-pyrrole-2,5-dione." Acta Crystallographica Section E Structure Reports Online 68, no. 5 (2012): o1328. http://dx.doi.org/10.1107/s1600536812014158.

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Köster, Roland, Günter Seidel, and Roland Boese. "Ethyl-substituierte 2,5-Dihydro-1,2,5-oxadiborole." Chemische Berichte 127, no. 11 (1994): 2159–65. http://dx.doi.org/10.1002/cber.1491271111.

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Shi, Da-Xin, Ya-Qing Feng, Xiao-Fang Li, and Li-Shan Zhou. "2-Benzyl-5-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-2,3-dihydro-1H-isoindole-1,3-dione." Acta Crystallographica Section E Structure Reports Online 59, no. 7 (2003): o1068—o1069. http://dx.doi.org/10.1107/s1600536803014181.

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Yamaguchi, Seiji. "3-Methyl-2,5-dihydro-1-benzoxepins and 3-Methyl-2,5-dihydrooxepins." HETEROCYCLES 79, no. 1 (2009): 243. http://dx.doi.org/10.3987/rev-08-sr(d)9.

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Dissertations / Theses on the topic "(dihydro-2,5)"

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Kapakli, Fadile. "New Strategy For The Synthesis Of Chiral N-substituted-3,4-dialkoxypyrrole From 2,5-dihydro-2,5-dimethoxyfuran." Master's thesis, METU, 2006. http://etd.lib.metu.edu.tr/upload/3/12607334/index.pdf.

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NEW STRATEGY FOR THE SYNTHESIS OF CHIRAL N-SUBSTITUTED-3,4-DIALKOXYPYRROLE FROM 2,5-DIHYDRO-2,5-DIMETHOXYFURAN KAPAKLI, FADiLE M.S., Department of Chemistry Supervisor : Prof. Dr. Cihangir Tanyeli July 2006, 80 pages Pyrroles are very valuable class of substances which have wide usage area in organic synthesis. In this study, chiral 3,4-dialkoxy-N-substituted pyrrole derivatives were synthesized. These compounds are widely used as building blocks for the synthesis of natural compounds that have focused on heterocyclic rings in their structures. In addition, chiral pyrrole derivatives can
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Grenier, Jérôme. "Synthèse et réactivité de sels et ylures de 2,5-dihydro-phospholium. Applications à la synthèse de composés di- et triéniques." Montpellier 2, 1995. http://www.theses.fr/1995MON20219.

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Nous decrivons la synthese de nouveaux sels de la famille des 1,1-diphenyl-2,5-dihydro-phospholium, avec de bons rendements, par l'adaptation des methodes decrites dans la litterature. Nous montrons que la synthese des monoylures depend etroitement des substituants en position 3,4 des sels correspondants. Quant a la synthese des diylures, elle semble s'averer impossible, du fait de l'attaque nucleophile du nbuli sur le cycle avec ouverture de ce dernier. Enfin, nous avons mis en evidence la potentialite de ces sels en tant que precurseurs d'oxydes de phosphine penta-2,4-dieniques et de 1,3,5-t
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Mehmandoust, Maryam. "Synthèse de dihydro-1, 2 pyridines et d'équivalents de sels de dihydro-2, 5 pyridinium à partir d'amines primaires chirales : application à la synthèse énantiosélective de dérivés d'isoquinuclidines et de pipéridines 2-substituées." Paris 11, 1989. http://www.theses.fr/1989PA112254.

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Une méthode générale de synthèse des sels de pyridinium N-substitués par différents auxiliaires chiraux, une application de la réaction de Zincke, à partir des amines primaires chirales correspondantes, est décrite. Par réduction au borohydrure de sodium en milieu alcalin, ces sels de pyridinium conduisent aux dihydro-1,2 pyridines correspondantes dont les réactions de cycloaddition avec l'acrylate de méthyle ont été étudiées. Des composés azabicyclo[2. 2. 2]octane (isoquinuclidines), dont la configuration absolue a été établie, sont obtenus avec des e. D. De 20 à 33% et une bonne pureté optiq
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Peine, Anja Stefanie [Verfasser]. "Auswirkungen des Duftstoffes 2,5-dihydro-2,4,5-trimethylthiazolin auf das räumliche Lernverhalten und die mRNA Expression von cFos und dem Corticotropin Releasing Factor in einem Glutamat-Decarboxylase67-Mausmodell / Anja Stefanie Peine." Magdeburg : Universitätsbibliothek, 2017. http://d-nb.info/1141230429/34.

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Tholé, France. "Étude d'une synthèse totale énantiosélective et convergente des liposidomycines." Paris 6, 2002. http://www.theses.fr/2002PA066352.

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Francese, Catherine. "Reactions du bromotrifluoromethane en presence de zinc : trifluoromethylations dans les conditions de barbier." Paris 6, 1987. http://www.theses.fr/1987PA066381.

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Cheng, Chih-Tien, and 鄭智恬. "Measurements for the Dissociation Conditions ofMethane Hydrate in the Presence of 2,5-Dihydrofuran,3,4-Dihydro-2H-pyran and Isopropylamine." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/93264841547431454674.

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碩士<br>國立臺灣大學<br>化學工程學研究所<br>99<br>This study demonstrated the equilibrium conditions for the formation of methane hydrates in the presence of cyclic ethers and alkyl amine, i.e. 2,5-dihydrofuran, 3,4-dihydro-2H-pyran and isopropylamine. The three-phase (H-Lw-V) and the four-phase (H-Lw-La-V) equilibrium data in methane + water + additives systems were measured by using isochoric method in the range of pressures from 6 to 12 MPa and temperature up to 301 K. When 2,5-dihydrofuran, 3,4-dihydro-2H-pyran and isopropylamine were added into methane hydrates systems respectively, the hydrate equilibri
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Book chapters on the topic "(dihydro-2,5)"

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "97 C4H7N 2,5-Dihydro-1H-pyrrole." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_98.

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Enchev, Dobromir D. "Synthesis and Biological Activity of 2,5-Dihydro-1,2-Oxaphosphole-2-Oxide Derivatives." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/7081_2009_4.

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Winkelmann, Jochen. "Diffusion coefficient of 3-(aminocarbonyl)-2,5-dihydro-2,2,5,5-tetramethyl-1H-pyrrol-1-yloxy in propane-1,2,3-triol." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_854.

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Heydt, H. "Of 2,5-Dihydro-1,3,4-oxadiazoles." In Heteroatom Analogues of Aldehydes and Ketones. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00779.

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"2,5-Dihydro-1,3,5-oxazaarsole to 4,5-Dihydro-1,2,3-thiadiazole." In Substance Index, edited by Backes, Fröhlich, and Pedeken. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-114072.

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"2,5-Dihydro-1,2,4-triazine to 1,4-Dihydro-1,3,5-triazine." In Substance index, edited by Backes, Fröhlich, and Padeken. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-114310.

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Aggarwal, P., and M. W. P. Bebbington. "Synthesis of 2,5-Dihydro-1,2,3-triazines." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00190.

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Grainger, R. S., and P. J. Jervis. "Dienes from 2,5-Dihydro-1-pyrroles." In 1,3-Dienes. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-046-00240.

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"2,5-Dihydro-1,3,5,2-triazaphosphorine to Cycloheptane." In Substance index, edited by Backes, Fröhlich, and Padeken. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-114313.

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"1,3-oxazole to 2,5-Dihydro-1,2-oxatitanole." In Substance Index, edited by Backes, Fröhlich, and Pedeken. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-114056.

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Conference papers on the topic "(dihydro-2,5)"

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Jansa, Petr, Martin Maxmilian Kaiser, Antonín Holý, and Zlatko Janeba. "A novel, highly stereoselective synthetic approach for the preparation of substituted 2,5-dihydro-2,5-dihydroxyfurans." In XVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112339.

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Skolaut, Alexander, and János Rétey. "3-(2,5-Cyclohexadienyl)-L-alanine (1,4-Dihydro-L-phenylalanine) - Its Synthesis and Behaviour in the Phenylalanine Ammonia-Lyase Reaction." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01834.

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You might also be interested in the extended bibliographies on the topic '(dihydro-2,5)' for particular source types:
Journal articles
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