Статті в журналах з теми "Bis-adducts"
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Tagliatesta, Pietro, Angelo Lembo, Valentina Orlandi та Marzia Nuccetelli. "Synthesis and characterization of new β-disubstituted porphyrin-[60]fullerene cyclic bis-adducts". Journal of Porphyrins and Phthalocyanines 14, № 08 (серпень 2010): 727–31. http://dx.doi.org/10.1142/s1088424610002537.
Повний текст джерелаYusifli, F. Kh, N. A. Aliyeva, and G. A. Ramazanov. "USE OF BIS-ADDUCTS OF ETHANEDITHIOL WITH ALKYL- AND CYCLOALKYL SUBSTITUTED METHYLENE DIOXOLANES IN THE COMPOSITION OF POLYVINYL CHLORIDE." Chemical Problems 21, no. 1 (2023): 72–77. http://dx.doi.org/10.32737/2221-8688-2023-1-72-77.
Повний текст джерелаSharma, Mousami, Anju Sharma, and Renu Sachar. "Synthesis and Characterization of the Adducts of Morpholinedithioccarbamate Complexes of Oxovanadium (IV), Nickel(II), and Copper(II) with Piperidine and Morpholine." E-Journal of Chemistry 9, no. 4 (2012): 1929–40. http://dx.doi.org/10.1155/2012/689501.
Повний текст джерелаBaer-Dubowska, W. "Alternative pathways of polycyclic aromatic hydrocarbons activation: the formation of polar DNA adducts." Acta Biochimica Polonica 46, no. 2 (June 30, 1999): 263–74. http://dx.doi.org/10.18388/abp.1999_4160.
Повний текст джерелаHossain, MM, ME Halim, MM Islam, K. Akhter, SM Ahmed, UKR Romman, and MG Ahmed. "Michael 1:1 adducts by acid catalyzed reaction during synthesis of spiro and spiroketal compounds." Bangladesh Journal of Scientific and Industrial Research 55, no. 4 (December 27, 2020): 283–88. http://dx.doi.org/10.3329/bjsir.v55i4.50967.
Повний текст джерелаKour, Gurpreet, Inderjeet Kour, and Renu Sachar. "Synthesis and Characterization of the Adducts of Bis(O-ethyldithiocarbonato)copper(II) with Substituted Pyridines." International Journal of Inorganic Chemistry 2013 (December 22, 2013): 1–4. http://dx.doi.org/10.1155/2013/502856.
Повний текст джерелаBispinghoff, Mark, Aaron M. Tondreau, Hansjörg Grützmacher, Charly A. Faradji, and Paul G. Pringle. "Carbene insertion into a P–H bond: parent phosphinidene–carbene adducts from PH3 and bis(phosphinidene)mercury complexes." Dalton Transactions 45, no. 14 (2016): 5999–6003. http://dx.doi.org/10.1039/c5dt01741f.
Повний текст джерелаSedenkova, Kseniya N., Elena B. Averina, Yuri K. Grishin, Julia V. Kolodyazhnaya, Victor B. Rybakov, Tamara S. Kuznetsova, Audrey Hughes, Gabriel dos Passos Gomes, Igor V. Alabugin, and Nikolay S. Zefirov. "Substituent effects on stereoselectivity of dihalocarbene reactions with cyclohexadiene and on the reactivity of bis-dihalocyclopropanes in electrophilic nitrations en route to pyrimidine N-oxides." Organic & Biomolecular Chemistry 15, no. 44 (2017): 9433–41. http://dx.doi.org/10.1039/c7ob02463k.
Повний текст джерелаWang, Guowei, Linghua Zhuang, and Jintang Wang. "A Route to a Tetrabenzothiazole from Michael Bis-Addition Compounds." Journal of Chemical Research 2009, no. 4 (April 2009): 212–13. http://dx.doi.org/10.3184/030823409x435883.
Повний текст джерелаTalbi, Arbia, Aïcha Arfaoui, Talia Bsaibess, Mohamed Lotfi Efrit, Anne Gaucher, Damien Prim та Hédi M′Rabet. "Selective synthesis of mono- and bis-butenolide α-aminomethyl adducts". Organic & Biomolecular Chemistry 15, № 15 (2017): 3298–303. http://dx.doi.org/10.1039/c7ob00206h.
Повний текст джерелаSchüler, Philipp, Helmar Görls, Matthias Westerhausen, and Sven Krieck. "Bis(trimethylsilyl)amide complexes of s-block metals with bidentate ether and amine ligands." Dalton Transactions 48, no. 24 (2019): 8966–75. http://dx.doi.org/10.1039/c9dt01426h.
Повний текст джерелаTrinh, Thi Minh Nguyet, Franck Schillinger, Sebastiano Guerra, Eric Meichsner, Iwona Nierengarten, Uwe Hahn, Michel Holler, and Jean‐François Nierengarten. "Regioselective Preparation of Fullerene Bis‐adducts from Cleavable Macrocyclic Bis‐malonates." European Journal of Organic Chemistry 2021, no. 27 (June 22, 2021): 3770–86. http://dx.doi.org/10.1002/ejoc.202100571.
Повний текст джерелаBenelli, C., D. Gatteschi, C. Zanchini, R. J. Doedens, M. H. Dickman, and L. C. Porter. "EPR spectra of bis(nitroxyl) adducts of bis(hexafluoroacetylacetonato)manganese(II)." Inorganic Chemistry 25, no. 19 (September 1986): 3453–57. http://dx.doi.org/10.1021/ic00239a027.
Повний текст джерелаMüller, Christoph, Sven Krieck, Helmar Görls, and Matthias Westerhausen. "Synthesis of Lewis Base Adducts of Barium Bis[bis(trimethylsilyl)amide]." European Journal of Inorganic Chemistry 2016, no. 28 (September 1, 2016): 4637–42. http://dx.doi.org/10.1002/ejic.201600561.
Повний текст джерелаBorisova, Kseniya K., Eugeniya V. Nikitina, Roman A. Novikov, Victor N. Khrustalev, Pavel V. Dorovatovskii, Yan V. Zubavichus, Maxim L. Kuznetsov, Vladimir P. Zaytsev, Alexey V. Varlamov, and Fedor I. Zubkov. "Diels–Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control." Chemical Communications 54, no. 23 (2018): 2850–53. http://dx.doi.org/10.1039/c7cc09466c.
Повний текст джерелаSellmann, Dieter, Marcus Hannakam, Falk Knoch, and Matthias Moll. "Übergangsmetallkomplexe mit Schwefelliganden, XCII. Oxidation von Thiolat-Amin- zu Schiffbase-Eisen(II)-Komplexen. Röntgenstrukturanalyse und Reaktivität von [Fe('N2S2')]2 (′N2S2′2- = Glyoxal-bis(2-mercaptoanil)(2 – )) / Transition Metal Complexes with Sulfur Ligands, XCII. Oxidation of Thiolate Amine to Schiff Base Iron(II) Complexes. X-Ray Structure Analysis and Reactivity of [Fe(′N2S2')]2 (′N2S2′2- = Glyoxal-bis(2-mercaptoanil)(2–))." Zeitschrift für Naturforschung B 47, no. 11 (November 1, 1992): 1545–50. http://dx.doi.org/10.1515/znb-1992-1107.
Повний текст джерелаYan, Xing-Xing, Chuang Niu, Shi-Qi Ye, Bo-Chen Zhao, and Guan-Wu Wang. "Electrochemically Promoted Benzylation of [60]Fullerooxazolidinone." Nanomaterials 12, no. 13 (July 1, 2022): 2281. http://dx.doi.org/10.3390/nano12132281.
Повний текст джерелаUmeyama, Tomokazu, Shogo Takahara, Sho Shibata, Kensho Igarashi, Tomohiro Higashino, Kenji Mishima, Koichi Yamashita, and Hiroshi Imahori. "cis-1 Isomers of tethered bismethano[70]fullerene as electron acceptors in organic photovoltaics." RSC Advances 8, no. 33 (2018): 18316–26. http://dx.doi.org/10.1039/c8ra02896f.
Повний текст джерелаTaylor, Laurence J., Brian A. Surgenor, Piotr Wawrzyniak, Matthew J. Ray, David B. Cordes, Alexandra M. Z. Slawin, and Petr Kilian. "Spontaneous dehydrocoupling in peri-substituted phosphine–borane adducts." Dalton Transactions 45, no. 5 (2016): 1976–86. http://dx.doi.org/10.1039/c5dt02539g.
Повний текст джерелаSølling, Theis I., та Leo Radom. "Exchange of Cl+ between Lone-Pair Donors and π-Donors: A Computational Study". European Journal of Mass Spectrometry 6, № 2 (квітень 2000): 153–60. http://dx.doi.org/10.1255/ejms.335.
Повний текст джерелаCharykov, N. A., V. A. Keskinov, and A. V. Petrov. "Adducts of Lower Fullerenes and Amino Acids: Synthesis, Identification, and Quantum-Mechanical Modeling of Their Physicochemical Properties." Russian Journal of Physical Chemistry A 95, no. 12 (December 2021): 2359–74. http://dx.doi.org/10.1134/s0036024421120049.
Повний текст джерелаAli, Shamsher, Eric Hénon, Ritchy Leroy, and Georges Massiot. "Addition of Vindoline to p-Benzoquinone: Regiochemistry, Stereochemistry and Symmetry Considerations." Molecules 26, no. 21 (October 22, 2021): 6395. http://dx.doi.org/10.3390/molecules26216395.
Повний текст джерелаSoleimani, Ebrahim, Katherine N. Robertson, Cory C. Pye, and Jason A. C. Clyburne. "Homolytic cleavage of Lawesson's reagent: N-heterocyclic carbene complexes of ArPS2 (Ar = 4-CH3O-C6H4)." Dalton Transactions 47, no. 18 (2018): 6299–303. http://dx.doi.org/10.1039/c8dt00457a.
Повний текст джерелаErber, Luke, Samantha Goodman, Caitlin Jokipii Krueger, Ivan Rusyn, and Natalia Tretyakova. "Quantitative NanoLC/NSI+-HRMS Method for 1,3-Butadiene Induced bis-N7-guanine DNA-DNA Cross-Links in Urine." Toxics 9, no. 10 (October 2, 2021): 247. http://dx.doi.org/10.3390/toxics9100247.
Повний текст джерелаEder, Erwin, and Christian Hoffman. "Identification and characterization of deoxyguanosine-crotonaldehyde adducts. Formation of 7,8 cyclic adducts and 1,N2,7,8-bis-cyclic adducts." Chemical Research in Toxicology 5, no. 6 (November 1992): 802–8. http://dx.doi.org/10.1021/tx00030a012.
Повний текст джерелаDo, Thomas H., and Seth N. Brown. "Mono- and bimetallic pentacoordinate silicon complexes of a chelating bis(catecholimine) ligand." Dalton Transactions 48, no. 30 (2019): 11565–74. http://dx.doi.org/10.1039/c9dt02475a.
Повний текст джерелаÐorđević, Luka, Lorenzo Casimiro, Nicola Demitri, Massimo Baroncini, Serena Silvi, Francesca Arcudi, Alberto Credi, and Maurizio Prato. "Light‐Controlled Regioselective Synthesis of Fullerene Bis‐Adducts." Angewandte Chemie International Edition 60, no. 1 (September 17, 2020): 313–20. http://dx.doi.org/10.1002/anie.202009235.
Повний текст джерелаSchmidbaur, Hubert, Wolfgang Bublak, Brigitte Huber, and Gerhard Müller. "Arene Adducts with Weak Interactions: Hexaethylbenzene–bis(tribromoarsane)." Angewandte Chemie International Edition in English 26, no. 3 (March 1987): 234–36. http://dx.doi.org/10.1002/anie.198702341.
Повний текст джерелаÐorđević, Luka, Lorenzo Casimiro, Nicola Demitri, Massimo Baroncini, Serena Silvi, Francesca Arcudi, Alberto Credi, and Maurizio Prato. "Light‐Controlled Regioselective Synthesis of Fullerene Bis‐Adducts." Angewandte Chemie 133, no. 1 (September 17, 2020): 317–24. http://dx.doi.org/10.1002/ange.202009235.
Повний текст джерелаAskari, Syed, Susan Lee, Robert R. Perkins, and John R. Scheffer. "Trapping of o-quinodimethane with p-quinones: synthesis of tetrahydro-1,4-anthracenediones." Canadian Journal of Chemistry 63, no. 12 (December 1, 1985): 3526–29. http://dx.doi.org/10.1139/v85-578.
Повний текст джерелаAsghar, Basim H. M., Michael R. Crampton та Chukwuemeka Isanbor. "Carbanion reactivity — σ-adduct formation and elimination in the reactions of the carbanion from bis(phenylsulfonyl)methane with 4-nitrobenzofurazan derivatives". Canadian Journal of Chemistry 86, № 3 (1 березня 2008): 225–29. http://dx.doi.org/10.1139/v08-010.
Повний текст джерелаFarquharson, Melvin J., and J. Stephen Hartman. "Bis(tertiary amine)dihaloboron cations and related species: nuclear magnetic resonance and fast atom bombardment mass spectrometry studies." Canadian Journal of Chemistry 67, no. 11 (November 1, 1989): 1711–23. http://dx.doi.org/10.1139/v89-264.
Повний текст джерелаDent, BR, B. Halton, and AMF Smith. "Synthesis and Trapping of Some Reactive Cyclopropenes." Australian Journal of Chemistry 39, no. 10 (1986): 1621. http://dx.doi.org/10.1071/ch9861621.
Повний текст джерелаSchumann, Herbert, Mario Glanz, Jochen Gottfriedsen, Sebastian Dechert, and Dietmar Wolff. "Lewis-acidic organometallic compounds of the lanthanides and the alkaline earth metals as catalysts for the activation of carbonyl groups." Pure and Applied Chemistry 73, no. 2 (January 1, 2001): 279–82. http://dx.doi.org/10.1351/pac200173020279.
Повний текст джерелаKohyama, Aki, Michihiro Fukuda, Shunsuke Sugiyama, Hiroyuki Yamakoshi, Naoki Kanoh, Chikashi Ishioka, Hiroyuki Shibata, and Yoshiharu Iwabuchi. "Reversibility of the thia-Michael reaction of cytotoxic C5-curcuminoid and structure–activity relationship of bis-thiol-adducts thereof." Organic & Biomolecular Chemistry 14, no. 45 (2016): 10683–87. http://dx.doi.org/10.1039/c6ob01771a.
Повний текст джерелаJones, Peter G., Jerzy Ossowski, Piotr Kus, and Ina Dix. "Three Crystal Structures of Terephthalic Acid Salts of Simple Amines." Zeitschrift für Naturforschung B 64, no. 7 (July 1, 2009): 865–70. http://dx.doi.org/10.1515/znb-2009-0716.
Повний текст джерелаMerlino, Antonello, Cinzia Verde, Guido di Prisco, Lelio Mazzarella, and Alessandro Vergara. "Reduction of ferric hemoglobin fromTrematomus bernacchiiin a partial bis-histidyl state produces a deoxy coordination even when encapsulated into the crystal phase." Spectroscopy 22, no. 2-3 (2008): 143–52. http://dx.doi.org/10.1155/2008/328463.
Повний текст джерелаDatta, R. N., A. H. M. Schotman, A. J. M. Weber, F. G. H. van Wijk, P. J. C. van Haeren, J. W. Hofstraat, A. G. Talma, and A. G. V. D. Bovenkamp-Bouwman. "Biscitraconimides as Anti-Reversion Agents for Diene Rubbers: Spectroscopic Studies on Citraconimide-Squalene Adducts." Rubber Chemistry and Technology 70, no. 1 (March 1, 1997): 129–45. http://dx.doi.org/10.5254/1.3538413.
Повний текст джерелаDickie, Diane A., Raymond P. Ulibarri-Sanchez, and Richard A. Kemp. "Zwitterionic CS2 Adducts of Bis(dialkylphosphino)amines: Syntheses, Spectroscopy, and Structures." Australian Journal of Chemistry 68, no. 3 (2015): 351. http://dx.doi.org/10.1071/ch14535.
Повний текст джерелаDickman, Michael H., Leigh C. Porter, and Robert J. Doedens. "Bis(nitroxyl) adducts of bis(hexafluoroacetylacetonato)manganese(II). Preparation, structures, and magnetic properties." Inorganic Chemistry 25, no. 15 (July 1986): 2595–99. http://dx.doi.org/10.1021/ic00235a022.
Повний текст джерелаRuiz, David A., Mohand Melaimi, and Guy Bertrand. "An efficient synthetic route to stable bis(carbene)borylenes [(L1)(L2)BH]." Chem. Commun. 50, no. 58 (2014): 7837–39. http://dx.doi.org/10.1039/c4cc03497j.
Повний текст джерелаSigl, Marcus, Annette Schier, and Hubert Schmidbaur. "Indium Triiodide Complexes of Bis(diphenyIphosphino)ethane (dppe) and its Disulfide (dppeS2)." Zeitschrift für Naturforschung B 54, no. 1 (January 1, 1999): 21–25. http://dx.doi.org/10.1515/znb-1999-0107.
Повний текст джерелаPal, Rammohan, Arpita Das Gupta та Asok K. Mallik. "Facile Iodine-Catalyzed Michael Addition of Indoles to α,α′-Bis(arylmethylene)cyclopentanones: An Efficient Synthesis of E-2-(3-Indolylphenylmethyl)-5-phenylmethylenecyclopentanones". ISRN Organic Chemistry 2012 (28 листопада 2012): 1–6. http://dx.doi.org/10.5402/2012/674629.
Повний текст джерелаTiu, Elisha G. V., Korinne Liosi, Safwan Aroua, and Yoko Yamakoshi. "Micelle vs. vesicle formation controlled by distal functionalization of C60–PEG conjugates." Journal of Materials Chemistry B 5, no. 32 (2017): 6676–80. http://dx.doi.org/10.1039/c7tb00829e.
Повний текст джерелаCameron, Donald W., Raymond L. Evans, Geoffrey I. Feutrill, Vincent A. Patrick, Brian W. Skelton, and Allan H. White. "Stereochemistry and Crystal Structures of Bis Cycloadducts of Danishefsky's Diene (Me3SiOC(=CH2)CH=CHOMe) with 2,5- and 2,6-Dichlorobenzoquinone." Australian Journal of Chemistry 56, no. 12 (2003): 1215. http://dx.doi.org/10.1071/ch03150.
Повний текст джерелаVillarejo, A. L. Doadrio, C. V. Ragel, and G. Pérez Cuevas. "bis (Xylenedithiocarboxylate)oxovanadium(IV) and Adducts with Organic Bases." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 22, no. 5 (May 1992): 599–614. http://dx.doi.org/10.1080/15533179208020232.
Повний текст джерелаMartin, Eddy, William Clegg, Ross W. Harrington, David L. Hughes, Michael B. Hursthouse, Louise Male, and Simon J. Lancaster. "Pyridine and benzonitrile adducts of bis(4-nonafluorobiphenyl)zinc." Polyhedron 29, no. 1 (January 2010): 405–13. http://dx.doi.org/10.1016/j.poly.2009.06.018.
Повний текст джерелаYoshida, Kazuhiro, Shuichi Osawa, Kenji Monde, Masataka Watanabe, and Nobuyuki Harada. "Absolute Stereochemistry of Chiral C 60 Fullerene Bis-Adducts." Enantiomer: A Journal of Sterochemistry 7, no. 1 (January 2002): 23–32. http://dx.doi.org/10.1080/10242430210704.
Повний текст джерелаMilic, Dragana, and Maurizio Prato. "Fullerene Unsymmetrical Bis-Adducts as Models for Novel Peptidomimetics." European Journal of Organic Chemistry 2010, no. 3 (January 2010): 476–83. http://dx.doi.org/10.1002/ejoc.200900791.
Повний текст джерелаHubrich, Christopher, Axel Schulz, and Alexander Villinger. "Adducts of Gallium Trichloride and Bis(trimethylsilyl)sulfur Diimide." Zeitschrift für anorganische und allgemeine Chemie 633, no. 13-14 (October 2007): 2362–66. http://dx.doi.org/10.1002/zaac.200700245.
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