Статті в журналах з теми "Hexane Substitution"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Hexane Substitution".
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Silva, Gabriel Julio da, Julcelly Dayara de Oliveira Henriques, and Patricia Fazzio Martins Martinez. "Sugarcane wax extraction using hexane and limonene mixtures." Revista Engenharia na Agricultura - REVENG 30 (February 21, 2022): 13–18. http://dx.doi.org/10.13083/reveng.v30i1.13241.
Повний текст джерелаCravotto, Christian, Anne-Sylvie Fabiano-Tixier, Ombéline Claux, Maryline Abert-Vian, Silvia Tabasso, Giancarlo Cravotto, and Farid Chemat. "Towards Substitution of Hexane as Extraction Solvent of Food Products and Ingredients with No Regrets." Foods 11, no. 21 (October 28, 2022): 3412. http://dx.doi.org/10.3390/foods11213412.
Повний текст джерелаRapinel, Vincent, Aziadé Chemat, Cyrille Santerre, Justine Belay, Farnaz Hanaei, Nadine Vallet, Laurence Jacques, and Anne-Sylvie Fabiano-Tixier. "2-Methyloxolane as a Bio-Based Solvent for Green Extraction of Aromas from Hops (Humulus lupulus L.)." Molecules 25, no. 7 (April 9, 2020): 1727. http://dx.doi.org/10.3390/molecules25071727.
Повний текст джерелаWalton, John C. "Radical rearrangements of bicyclo[2.2.0]hexane: homolytic substitution of a cyclobutane ring." Journal of the Chemical Society, Chemical Communications, no. 16 (1987): 1252. http://dx.doi.org/10.1039/c39870001252.
Повний текст джерелаKeglevich, György, Attila Kovács, László Tőke, Kálmán Újszászy, Gyula Argay, Mátyás Czugler, and Alajos Kálmán. "P-Substituted 3-phosphabicyclo [3.1.0] hexane 3-oxides from diastereoselective substitution at phosphorus." Heteroatom Chemistry 4, no. 4 (August 1993): 329–35. http://dx.doi.org/10.1002/hc.520040405.
Повний текст джерелаGardecka, A. J., G. K. L. Goh, G. Sankar, and I. P. Parkin. "On the nature of niobium substitution in niobium doped titania thin films by AACVD and its impact on electrical and optical properties." Journal of Materials Chemistry A 3, no. 34 (2015): 17755–62. http://dx.doi.org/10.1039/c5ta03772g.
Повний текст джерелаHung, Nguyen Khanh, Nguyen Tuan Thanh, Nguyen Thi Thuy Luyen, and Nguyen Huy Du. "Evaluating the enantioselective capability of a cellulose tris(3,5‐dimethylphenyl carbamate)‐based stationary phase towards 5,7,2'‐trihydroxyflavanone." Vietnam Journal of Chemistry 61, S2 (November 2023): 149–54. http://dx.doi.org/10.1002/vjch.202300193.
Повний текст джерелаShahin, Nabil, Nawaf Abu-Khalaf, Mazen Salman, and Harun Parlar. "Testing the Possibility of Photochemical Synthesis of Chlorinated Phenols, Benzenes and Biphenyl: Pre-study Guide for Standards Synthesis." مجلة جامعة فلسطين التقنية للأبحاث 4, no. 2 (September 1, 2016): 73–83. http://dx.doi.org/10.53671/pturj.v4i2.47.
Повний текст джерелаShahin, Nabil, Nawaf Abu-Khalaf, Mazen Salman, and Harun Parlar. "Testing the Possibility of Photochemical Synthesis of Chlorinated Phenols, Benzenes and Biphenyl: Pre-study Guide for Standards Synthesis." مجلة جامعة فلسطين التقنية خضوري للأبحاث 4, no. 2 (September 1, 2016): 73–83. http://dx.doi.org/10.53671/ptukrj.v4i2.47.
Повний текст джерелаFischer, Malte, Marc Schmidtmann та Rüdiger Beckhaus. "Crystal structure of the formal 20 electron zirconocene pentafulvene complex Cp2Zr(η5,η1-adamantylidenepentafulvene):toluene:n-hexane = 1:0.125:0.125". Acta Crystallographica Section E Crystallographic Communications 73, № 12 (3 листопада 2017): 1823–26. http://dx.doi.org/10.1107/s2056989017015560.
Повний текст джерелаMaha F. Abbass, Salah Al-Shukri, and Ahmed A. Ahmed. "Selective mono substitution of cyclotri-phosphazene by 2-Hydroxyethylacrylate producing new acrylate cyclo-triphosphazene." GSC Advanced Research and Reviews 10, no. 3 (March 30, 2022): 080–87. http://dx.doi.org/10.30574/gscarr.2022.10.3.0070.
Повний текст джерелаEngering, Josef, Eva-Maria Peters, and Martin Jansen. "Dimeres Di(N-lithium–tert–butylamino)bis(dimethylamino)silan - [Si(N(CH3)2)2(NLiC(CH3)3)2]2 – Darstellung und Kristallstruktur / Dimeric Di(N -lithio-tert-butylamino)bis(dimethylamino)silane - [Si(N(CH3)2)2(NLiC(CH3)3)2]2 – Synthesis und Crystal Structure." Zeitschrift für Naturforschung B 56, no. 1 (January 1, 2001): 90–94. http://dx.doi.org/10.1515/znb-2001-0115.
Повний текст джерелаKEGLEVICH, G., A. KOVACS, L. TOEKE, K. UJSZASZY, G. ARGAY, M. CZUGLER, and A. KALMAN. "ChemInform Abstract: P-Substituted 3-Phosphabicyclo(3.1.0)hexane 3-Oxides from Diastereoselective Substitution at Phosphorus." ChemInform 25, no. 2 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199402219.
Повний текст джерелаIstyami, Astri Nur, Tatang Hernas Soerawidjaja, Tirto Prakoso, and Tri Ari Penia Kresnowati. "Performance of Various Organic Solvents as Reaction Media in Plant Oil Lipolysis with Plant Lipase." Reaktor 18, no. 2 (August 24, 2018): 71. http://dx.doi.org/10.14710/reaktor.18.2.71-75.
Повний текст джерелаLanders, Gary M., and James A. Olson. "Absence of Isomerization of Retinyl Palmitate, Retinol, and Retinal in Chlorinated and Nonchlorinated Solvents Under Gold Light." Journal of AOAC INTERNATIONAL 69, no. 1 (January 1, 1986): 50–55. http://dx.doi.org/10.1093/jaoac/69.1.50.
Повний текст джерелаWloch, J. "Influence of isomorphous substitution in MFI-type materials on the diffusion of n-hexane: Molecular dynamic studies." Applied Surface Science 253, no. 13 (April 2007): 5692–95. http://dx.doi.org/10.1016/j.apsusc.2006.12.047.
Повний текст джерелаZapol’skii, Viktor A., Jan C. Namyslo, Armin de Meijere, and Dieter E. Kaufmann. "Chemistry of polyhalogenated nitrobutadienes, 10: Synthesis of highly functionalized heterocycles with a rigid 6-amino-3-azabicyclo[3.1.0]hexane moiety." Beilstein Journal of Organic Chemistry 8 (April 23, 2012): 621–28. http://dx.doi.org/10.3762/bjoc.8.69.
Повний текст джерелаCibian, Mihaela, André Bessette, Andrew O'Connor, Janaina G. Ferreira, and Garry S. Hanan. "Twofac-tricarbonylrhenium(I) azadipyrromethene (ADPM) complexes: ligand-substitution effect on crystal structure." Acta Crystallographica Section C Structural Chemistry 71, no. 2 (January 17, 2015): 122–27. http://dx.doi.org/10.1107/s2053229614027673.
Повний текст джерелаChiacchiera, Stella M., Joaqu�n O. Singh, Jorge D. Anunziata, and Juana J. Silber. "Aromatic nucleophilic substitution reactions of 1,2-dinitrobenzene with aliphatic primary amines in n-hexane; catalysis by non-nucleophilic bases." Journal of the Chemical Society, Perkin Transactions 2, no. 8 (1987): 987. http://dx.doi.org/10.1039/p29870000987.
Повний текст джерелаSingh, Joaquín O., Jorge D. Anunziata та Juana J. Silber. "n–π Electron donor–acceptor complexes. II. Aliphatic amines with dinitrobenzenes". Canadian Journal of Chemistry 63, № 4 (1 квітня 1985): 903–7. http://dx.doi.org/10.1139/v85-150.
Повний текст джерелаMinka, S., and M. Bruneteau. "Isolement et caractérisation chimique des lipopolysaccharides de type R dans une souche hypovirulente de Yersinia pestis." Canadian Journal of Microbiology 44, no. 5 (May 1, 1998): 477–81. http://dx.doi.org/10.1139/w98-029.
Повний текст джерелаEngering, Josef, Eva-Maria Peters, and Martin Jansen. "Synthesen und Kristallstrukturen von Bis(N-lithiumtrimethylsilylamino)- bis(dimethylamino)silan und 1,1-Dichloro-2,4-bis(trimethylsilylamino)- 3,3-bis(dimethylamino)siladiazatitanacyclobutan / Syntheses and Crystal Structures of Bis(N-lithio-trimethylsilylamino)bis(dimethylamino)- silane and 1,1-Dichloro-2,4-bis(trimethylsilylamino)-3,3-bis(dimethylamino)siladiazatitanacyclobutane." Zeitschrift für Naturforschung B 57, no. 9 (September 1, 2002): 976–82. http://dx.doi.org/10.1515/znb-2002-0902.
Повний текст джерелаOllivier, Jean, Frédéric Lecornué та Florence Charnay-Pouget. "π-Allyl Palladium Complexes as Efficient and Powerful Alternative for Nucleophilic Substitution on Bicyclo[3.1.0]hexane Sulfonates: Regio-, Chemo- and Stereoselectivity". Synlett 2006, № 9 (червень 2006): 1407–9. http://dx.doi.org/10.1055/s-2006-939716.
Повний текст джерелаLeigh, William J., Andrey G. Moiseev, Eugenie Coulais, Farahnaz Lollmahomed, and Mohammad S. Askari. "Substituent effects on silene reactivity — Reactive silenes from photolysis of phenylated tri- and tetrasilanes." Canadian Journal of Chemistry 86, no. 12 (December 1, 2008): 1105–17. http://dx.doi.org/10.1139/v08-165.
Повний текст джерелаBudiarti, Mery, Anshary Maruzy, Nengah Ratri RK, and Endang Brotojoyo. "Aktivitas Antimalaria Daun Gempol (Nauclea orientalis (L.) L) terhadap Plasmodium falciparum." Media Penelitian dan Pengembangan Kesehatan 30, no. 2 (September 30, 2020): 135–46. http://dx.doi.org/10.22435/mpk.v30i2.3044.
Повний текст джерелаIdo, Atsushi, Atsushi Hashizume, Takashi Ohta, Takayuki Takahashi, Chiemi Miura, and Takeshi Miura. "Replacement of Fish Meal by Defatted Yellow Mealworm (Tenebrio molitor) Larvae in Diet Improves Growth Performance and Disease Resistance in Red Seabream (Pargus major)." Animals 9, no. 3 (March 19, 2019): 100. http://dx.doi.org/10.3390/ani9030100.
Повний текст джерелаMarliyana, Surya Dewi, Sayekti Wahyuningsih, and Nisa Nur Hayati. "Synthesis of Cardanol-Based Acetaldehyde Novolac Resin from Cashew Nut Shell Liquid (CNSL)." Jurnal Kimia Sains dan Aplikasi 25, no. 9 (November 24, 2022): 316–21. http://dx.doi.org/10.14710/jksa.25.9.316-321.
Повний текст джерелаKrow, Grant R., Seth B. Herzon, Guoliang Lin, Feng Qiu, and Philip E. Sonnet. "Complex-Induced Proximity Effects. Temperature-Dependent Regiochemical Diversity in Lithiation−Electrophilic Substitution Reactions ofN-BOC-2-Azabicyclo[2.1.1]hexane. 2,4- and 3,5-Methanoprolines." Organic Letters 4, no. 18 (September 2002): 3151–54. http://dx.doi.org/10.1021/ol026509b.
Повний текст джерелаKim, Hak Sung, Michihiro Ohno, Bin Xu, Hea Ok Kim, Yongseok Choi, Xiao D. Ji, Savitri Maddileti, Victor E. Marquez, T. Kendall Harden, and Kenneth A. Jacobson. "2-Substitution of Adenine Nucleotide Analogues Containing a Bicyclo[3.1.0]hexane Ring System Locked in a Northern Conformation: Enhanced Potency as P2Y1Receptor Antagonists." Journal of Medicinal Chemistry 46, no. 23 (November 2003): 4974–87. http://dx.doi.org/10.1021/jm030127+.
Повний текст джерелаKEGLEVICH, G., L. TOEKE, A. KOVACS, K. UJSZASZY, G. ARGAY, M. CZUGLER, and A. KALMAN. "ChemInform Abstract: Ring Transformation of Phosphorus Containing Heterocycles. Part 12. P- Substituted 3-Phosphabicyclo(3.1.0)hexane 3-Oxides from Diastereoselective Substitution at Phosphorus." ChemInform 25, no. 52 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199452204.
Повний текст джерелаNeugebauer, Peter, Uwe Klingebiel, and Mathias Noltemeyer. "Silylfurane und Bis(silyl)butadiine -Synthese, Lithiumderivate, Kristallstrukturen/ Silylfurans and Bis(silyl)butadiynes - Synthesis, Lithium Derivatives, Crystal Structures." Zeitschrift für Naturforschung B 55, no. 10 (October 1, 2000): 913–23. http://dx.doi.org/10.1515/znb-2000-1005.
Повний текст джерелаPark, Hanna, Byeongho Kim, Kyoung-Chan Park, Yesun Kim, Taehee Kim, Min-Seok Kim, Sun-Eun Choi, and Se-Yeong Park. "Biological Activities in Sapwood and Heartwood Extractives from Paulownia tomentosa." Forests 14, no. 11 (October 31, 2023): 2171. http://dx.doi.org/10.3390/f14112171.
Повний текст джерелаRoacho, Robinson I., Alejandro Metta-Magaña, José L. Belmonte-Vázquez, Eduardo Peña-Cabrera, and Keith H. Pannell. "Formation of 8-RS-BODIPYs via direct substitution of 8-MeS-BODIPY by RSH (R = Et, Pr, Bu, tBu, n-C12H25, C6H5, p-MeC6H4, p-MeOC6H4, and 2,6-Me2C6H3)." Canadian Journal of Chemistry 94, no. 3 (March 2016): 234–39. http://dx.doi.org/10.1139/cjc-2015-0303.
Повний текст джерелаDella, EW, GM Elsey, and G. Skouroumounis. "Rearrangement of Substituted Bicyclo[2.1.1]hex-2-yl Mesylates Under Solvolytic Conditions." Australian Journal of Chemistry 43, no. 7 (1990): 1231. http://dx.doi.org/10.1071/ch9901231.
Повний текст джерелаDominguez, Carmen, Lourdes Prieto, Matthew J. Valli, Steven M. Massey, Mark Bures, Rebecca A. Wright, Bryan G. Johnson, et al. "Methyl Substitution of 2-Aminobicyclo[3.1.0]hexane 2,6-Dicarboxylate (LY354740) Determines Functional Activity at Metabotropic Glutamate Receptors: Identification of a Subtype Selective mGlu2 Receptor Agonist." Journal of Medicinal Chemistry 48, no. 10 (May 2005): 3605–12. http://dx.doi.org/10.1021/jm040222y.
Повний текст джерелаGinting, Mimpin. "Synthesis of 2-(4-Allyl-2-Methoxy Phenoxy)-N,N-Bis(2- Hydroxyethyl) Acetamide from the Transformation of Eugenol Isolated from Clove Oil." Journal of Chemical Natural Resources 1, no. 1 (February 28, 2019): 31–39. http://dx.doi.org/10.32734/jcnar.v1i1.832.
Повний текст джерелаKaur, Gunpreet, Vikas Gupta, R. G. Singhal, and Parveen Bansal. "Isolation and Characterization of Stigmasterol from Fritillaria roylei." Biology, Medicine, & Natural Product Chemistry 9, no. 2 (November 16, 2020): 77–80. http://dx.doi.org/10.14421/biomedich.2020.92.77-80.
Повний текст джерелаVakhitova, L. M., N. A. Taran, V. I. Bessarabov, R. A. Vakhitov, G. F. Rayenko, and A. F. Popov. "Rheologically improved microemulsion for deactivation of simulants of blister and nerve agents." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 6 (December 2023): 44–52. http://dx.doi.org/10.32434/0321-4095-2023-151-6-44-52.
Повний текст джерелаArnold, Deirdre I., F. Albert Cotton, John H. Matonic, and Carlos A. Murillo. "Substitution on a methyl group of an acetylacetonate ligand: synthesis and structural characterization of oxobis[6-(phenylamino)hexane-2,4-dionato-O,O′]vanadium(IV), VO(Phad)2." Chem. Commun., no. 18 (1996): 2113–14. http://dx.doi.org/10.1039/cc9960002113.
Повний текст джерелаJean-Baptiste, KANGAH Niameke, KODJO Charles Guillaume, OUATTARA Zana Adama, KABLAN Ahmont Landry Claude, DIBI Konan Jacques, KOUAME Bosson Antoine, and Ziao Nahosse. "Synthesis, Characterization and Biological Evaluation of New Series of Schiff Bases Derived from Hexamethylenediamine as Potential Antibacterial and Antifungal Agents." IRA-International Journal of Applied Sciences (ISSN 2455-4499) 7, no. 2 (May 27, 2017): 69. http://dx.doi.org/10.21013/jas.v7.n2.p3.
Повний текст джерелаAhmed, Tahseen, Ambreen Huma, Munnawar Rasheed, Mirza Tasawer Baig, Syed Shafqat Rizvi, Sadaf Gul, and Sadaf Ibrahim. "Pharmacognostic Standardization and Phycochemical Evaluation of Green Seaweed Codium Flabellatum." Journal of Hunan University Natural Sciences 49, no. 6 (June 30, 2022): 111–19. http://dx.doi.org/10.55463/issn.1674-2974.49.6.12.
Повний текст джерелаBrodie, Nancy M. J., and Anthony J. Poë. "Systematic substitution kinetics of the clusters Ru3(CO)11L and Ru3(CO)10L2 (L = P-donor ligands): The unimolecular path." Canadian Journal of Chemistry 73, no. 7 (July 1, 1995): 1187–95. http://dx.doi.org/10.1139/v95-146.
Повний текст джерелаBishimbayeva, G. K., A. M. Nalibayeva, S. A. Saidullayeva, A. K. Zhanabaeva, A. Bold, and Y. N. Abdikalykov. "Synthesis and study of the extraction properties ofnew phosphorus-containing extractants of heavy metals." Proceedings of Universities. Applied Chemistry and Biotechnology 11, no. 3 (October 7, 2021): 340–48. http://dx.doi.org/10.21285/2227-2925-2021-11-3-340-348.
Повний текст джерелаSzczęsna, Weronika, Marta Tsirigotis-Maniecka, Łukasz Lamch, Lilianna Szyk-Warszyńska, Ewa Zboińska, Piotr Warszyński, and Kazimiera A. Wilk. "Multilayered Curcumin-Loaded Hydrogel Microcarriers with Antimicrobial Function." Molecules 27, no. 4 (February 19, 2022): 1415. http://dx.doi.org/10.3390/molecules27041415.
Повний текст джерелаWächtler, Erik, Robert Gericke, Theresa Block, Birgit Gerke, Rainer Pöttgen, and Jörg Wagler. "Compounds of the types Pn(pyS)3 (Pn = P, As, Bi; pyS: pyridine-2-thiolate) and Sb(pyS) x Ph3–x (x = 3–1); molecular structures and electronic situations of the Pn atoms." Zeitschrift für Naturforschung B 76, no. 2 (January 15, 2021): 103–18. http://dx.doi.org/10.1515/znb-2020-0171.
Повний текст джерелаNakayama, Katsuyuki, Yuichi Kondo, and Koji Ishihara. "A kinetic study of the reactions of dimethyl sulfide bridged tetramethylplatinum(II) and octamethylplatinum(IV) complexes with dimethyl sulfide and bidentate ligands." Canadian Journal of Chemistry 76, no. 1 (January 1, 1998): 62–70. http://dx.doi.org/10.1139/v97-203.
Повний текст джерелаSundaramurthy, V., I. Eswaramoorthi, and N. Lingappan. "The catalytic effect of boron substitution in MCM-41-type molecular sieves." Canadian Journal of Chemistry 82, no. 5 (May 1, 2004): 631–40. http://dx.doi.org/10.1139/v04-017.
Повний текст джерелаWang, Qian, and Yuichi Kobayashi. "Allylic Substitution on Cyclopentene and -hexene Rings with Alkynylcopper Reagents." Organic Letters 13, no. 23 (December 2, 2011): 6252–55. http://dx.doi.org/10.1021/ol202711k.
Повний текст джерелаMaslivetc, Vladimir, Colby Barrett, Nicolai A. Aksenov, Marina Rubina, and Michael Rubin. "Intramolecular nucleophilic addition of carbanions generated from N-benzylamides to cyclopropenes." Organic & Biomolecular Chemistry 16, no. 2 (2018): 285–94. http://dx.doi.org/10.1039/c7ob02068f.
Повний текст джерелаDuczmal, Wojciech, Bogdan Marciniec, and Elżbieta Śliwinska. "Substitution of phosphine in the complex [RhCl(cyclooctadiene)(phosphine)] by 1-hexene." Transition Metal Chemistry 14, no. 2 (April 1989): 105–9. http://dx.doi.org/10.1007/bf01040601.
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