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Artículos de revistas sobre el tema "Addition compounds"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 25 de julio de 2025

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1

Laila, Arjuman Banu, and Saidul Islam M. "Addition compounds of AsIII, ShIII and BiIII halides with quinoline and iso-quinoline." Journal of Indian Chemical Society Vol. 83, Nov 2006 (2006): 1142–44. https://doi.org/10.5281/zenodo.5832482.

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Department of Chemistry. Rajshahi University, Rajshahi-6205, Bangladesh <em>Manuscript received 29 August 2005, revised 17 August 2006, accepted 21 August 2006</em> A few addition compounds of As<sup>III</sup>, Sb<sup>III</sup> and Bi<sup>III</sup> halides containing quinoline and iso-quinoline have been synthesized and characterized on the basis of elemental analysis, IR, UV, NMR and molar conductance studies. The complexes have the compositions [MX<sub>3</sub>.L], where M = As<sup>lll</sup>, Sb<sup>lll</sup> and Bi<sup>III</sup>, L = quinoline and iso-quinoline, X = Br<sup>-</sup>.Cl<sup>-</
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2

Lalama, Mark S., Jeff Kampf, David G. Dick, and John P. Oliver. "Structural Studies on Mesitylaluminum Addition Compounds." Organometallics 14, no. 1 (1995): 495–501. http://dx.doi.org/10.1021/om00001a067.

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3

Neidlein, Richard, Anna Rufińska, Harald Schwager, and Günther Wilke. "Nickelacyclobutabenzene Compounds by Oxidative Addition of Cyclopropabenzene to Nickel(0) Compounds." Angewandte Chemie International Edition in English 25, no. 7 (1986): 640–42. http://dx.doi.org/10.1002/anie.198606401.

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4

Cíchová, M., J. Petříček, and J. Fiala. "Influence of tannin addition on the content and composition of polyphenolic compounds in wines." Czech Journal of Food Sciences 26, Special Issue (2009): S33—S38. http://dx.doi.org/10.17221/242/2008-cjfs.

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Polyphenols can greatly affect the sensorial characteristics and stability of wine. The concentration of polyphenols in wines is very low, the sample must be thus concentrated before the analytical measurement. The extraction on solid phase (SPE) is a suitable method for the isolation, purification, and concentration of polyphenols from complicated matrices. RP-HPLC with diode array detection was used for the separation and identification of polyphenols. A library of absorption spectra of standards was created and used for the identification of 14 polyphenols in wines. The contents of the indi
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5

Hunt, David A. "MICHAEL ADDITION OF ORGANOLITHIUM COMPOUNDS. A REVIEW." Organic Preparations and Procedures International 21, no. 6 (1989): 705–49. http://dx.doi.org/10.1080/00304948909356219.

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6

Sewald, Norbert, and Audrius Rimkus. "Conjugate Addition of Organozinc Compounds to Nitroolefins." Synthesis 2004, no. 01 (2003): 135–46. http://dx.doi.org/10.1055/s-2003-44355.

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7

Hoge, Berthold, and Christoph Thösen. "Novel Addition of Diphosphanes to Carbonyl Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 177, no. 8-9 (2002): 2151–52. http://dx.doi.org/10.1080/10426500213437.

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8

Stepanov, A. A. "Electroinduced Addition of Fluoroalkyltrimethylsilanes to Carbonyl Compounds." Russian Journal of Electrochemistry 39, no. 11 (2003): 1201–2. http://dx.doi.org/10.1023/b:ruel.0000003446.18833.4b.

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9

Postovoi, S. A., E. M. Kagramanova, E. I. Mysov, and Yu V. Zeifman. "Reductive addition of polychlorofluoroalkanes to fluorocarbonyl compounds." Russian Chemical Bulletin 45, no. 6 (1996): 1425–27. http://dx.doi.org/10.1007/bf01434225.

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10

Rodriques, Karen E., Anwer Basha, James B. Summers, and Dee W. Brooks. "Addition of aryllithium compounds to oxime ethers." Tetrahedron Letters 29, no. 28 (1988): 3455–58. http://dx.doi.org/10.1016/0040-4039(88)85188-8.

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11

Bronk, Brian S., Stephen J. Lippard, and Rick L. Danheiser. "Intramolecular conjugate addition reactions via organozinc compounds." Organometallics 12, no. 8 (1993): 3340–49. http://dx.doi.org/10.1021/om00032a065.

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12

SERA, A. "ChemInform Abstract: Addition Reactions to Conjugated Compounds." ChemInform 22, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.199139300.

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13

Huan, Feng, Huawei Hu, Yangen Huang, Qingyun Chen, and Yong Guo. "Michael Addition Reaction of Fluorinated Nitro Compounds." Chinese Journal of Chemistry 30, no. 4 (2012): 798–802. http://dx.doi.org/10.1002/cjoc.201100412.

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14

Lépine, F. L., S. Milot, D. Boismenu, and O. A. Mamer. "Collision-induced oxygen addition to chloroaromatic compounds." Journal of the American Society for Mass Spectrometry 7, no. 11 (1996): 1144–50. http://dx.doi.org/10.1016/s1044-0305(96)00076-1.

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15

van Bruggen, E., H. Boelens, and F. Rijkens. "Free radical additions. Part I: Free radical addition of cyclo-octane to unsaturated compounds." Recueil des Travaux Chimiques des Pays-Bas 86, no. 9 (2010): 958–60. http://dx.doi.org/10.1002/recl.19670860906.

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16

TAKAI, Kazuhiko, and Hitosi NOZAKI. "Nucleophilic addition of organochromium reagents to carbonyl compounds." Proceedings of the Japan Academy. Ser. B: Physical and Biological Sciences 76, no. 8 (2000): 123–31. http://dx.doi.org/10.2183/pjab.76.123.

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17

Cardozo, Samuel D., Matthias Schulze, Rik R. Tykwinski, and Murray R. Gray. "Addition Reactions of Olefins to Asphaltene Model Compounds." Energy & Fuels 29, no. 3 (2015): 1494–502. http://dx.doi.org/10.1021/ef502616v.

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18

Kukharev, Boris F., Valery K. Stankevich, and Galina R. Klimenko. "Nucleophilic addition of secondary nitro compounds to acetylene." Mendeleev Communications 12, no. 2 (2002): 63–64. http://dx.doi.org/10.1070/mc2002v012n02abeh001541.

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19

Haas, A., M. Lieb, and Yuanfa Zhang. "Catalytic addition of trihalogenomethanesulfenyl chlorides to olefinic compounds." Journal of Fluorine Chemistry 30, no. 2 (1985): 203–10. http://dx.doi.org/10.1016/s0022-1139(00)80889-1.

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20

Alberti, Angelo, and Gian Franco Pedulli. "Addition reactions of silyl radicals to unsaturated compounds." Reviews of Chemical Intermediates 8, no. 2 (1987): 207–46. http://dx.doi.org/10.1007/bf03156140.

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21

Friestad, Gregory K., and Hui Ding. "Asymmetric Addition of Allylic Nucleophiles to Imino Compounds." Synthesis 2005, no. 17 (2005): 2815–29. http://dx.doi.org/10.1055/s-2005-872181.

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22

Rai, U. S., and K. D. Mandal. "Solidification Behaviour of Organic Eutectics and Addition Compounds." Materials Science Forum 50 (January 1991): 117–28. http://dx.doi.org/10.4028/www.scientific.net/msf.50.117.

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23

Yus, Miguel, and Diego J. Ramón. "Enantioselective addition of organozinc reagents to carbonyl compounds." Pure and Applied Chemistry 77, no. 12 (2005): 2111–19. http://dx.doi.org/10.1351/pac200577122111.

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Different chiral camphorsulfonamide derivatives containing a hydroxy or a sulfonamido functionality, as well as chiral 1,2-hydroxysulfonamides, have been evaluated as chiral promoters in the classical enantioselective addition of dialkylzinc reagents to aldehydes in the presence of titanium tetraisopropoxide (ee up to 96 %). Surprisingly, ligands with a structure of isoborneol are able to promote the related unknown addition to ketones (ee &gt;99 %), the best ligand being the exo-diol derived from 1,2-trans-biscamphorsulfonamidocyclohexane (HOCSAC).
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24

Aggarwal, Varinder K., and Andrea Mereu. "Amidine-Promoted Addition of Chloroform to Carbonyl Compounds." Journal of Organic Chemistry 65, no. 21 (2000): 7211–12. http://dx.doi.org/10.1021/jo000584n.

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25

Kasatkin, A. N., R. Kh Biktimirov, I. P. Podlipchuk, V. R. Sultanmuratova, and G. A. Tolstikov. "Diastereoselective addition of organomanganese compounds to ?-alkoxysubstituted propanals." Russian Chemical Bulletin 42, no. 1 (1993): 161–65. http://dx.doi.org/10.1007/bf00700000.

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26

Howie, R. Alan, Gavin M. Spencer, James L. Wardell, and John N. Low. "Addition of sulphenyl halides to alkenyl-metal compounds." Journal of Organometallic Chemistry 437, no. 1-2 (1992): 111–25. http://dx.doi.org/10.1016/0022-328x(92)83436-l.

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27

Lovinger, Gabriel J., and James P. Morken. "Recent Advances in Radical Addition to Alkenylboron Compounds." European Journal of Organic Chemistry 2020, no. 16 (2019): 2362–68. http://dx.doi.org/10.1002/ejoc.201901600.

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28

Kasatkin, A. N., I. P. Podlipchuk, R. K. Biktimirov, and G. A. Tolstikov. "Diastereoselective addition of organomanganese compounds to chiral polyalkoxyaldehydes." Russian Chemical Bulletin 42, no. 6 (1993): 1078–82. http://dx.doi.org/10.1007/bf00704203.

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29

Reetz, Manfred T., Jürgen Westermann, Rainer Steinbach, et al. "Chemoselective addition of organotitanium reagents to carbonyl compounds." Chemische Berichte 118, no. 4 (1985): 1421–40. http://dx.doi.org/10.1002/cber.19851180412.

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30

Reetz, Manfred T., Rainer Steinbach, Jürgen Westermann, Roland Peter, and Bernd Wenderoth. "Stereoselective Addition of Organotitanium Reagents to Carbonyl Compounds." Chemische Berichte 118, no. 4 (1985): 1441–54. http://dx.doi.org/10.1002/cber.19851180413.

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31

Chen, Jia-Rong, and Wen-Jing Xiao. "ChemInform Abstract: Addition to Carbonyl Compounds: Aldehydes/Ketones." ChemInform 41, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.201025250.

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32

Li, Junjie, and Qi Wang. "Radical addition-coupling polymerization with various nitroso compounds." Journal of Polymer Science Part A: Polymer Chemistry 52, no. 6 (2013): 810–15. http://dx.doi.org/10.1002/pola.27061.

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33

van der Veer, W., and F. Jellinek. "Adducts of thiophosphoryl compounds with metal halides. I.: Addition compounds of triphenylphosphine sulfide." Recueil des Travaux Chimiques des Pays-Bas 85, no. 8 (2010): 842–56. http://dx.doi.org/10.1002/recl.19660850813.

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34

Deng, Danfeng, Dayun Huang, Xiangyu Sun, and Biwen Gao. "Recent Advances in the Tandem Difunctionalization of Alkynes: Mechanism-Based Classification." Synthesis 53, no. 19 (2021): 3522–34. http://dx.doi.org/10.1055/a-1486-2158.

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AbstractRecent advances on the tandem difunctionalization of alkynes in the last decade (2010–2020) are summarized into five categories based on the type of mechanism: (1) radical addition and coupling for the synthesis of polysubstituted ketones and alkenes, (2) electrophilic addition of alkynes, (3) reactions mediated by haloalkynes or copper acetylides, (4) the preparation of cyclic compounds via radical processes, palladium-catalyzed reactions or conjugate additions, and (5) cyclic compounds as intermediates in ring openings. Herein, radical, electrophilic and nucleophilic reactions are di
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35

D., K. DUTTA, and M. SINGH M. "Oxidative Addition and Adduct Formation Reaction of Carbonyl Compounds of Rhodium(I)." Journal of Indian Chemical Society Vol. 65, Apr 1988 (1988): 235–37. https://doi.org/10.5281/zenodo.6010464.

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Department of Chemistry, Dibrugarh University, Dibrugarh-786 004 <em>Manuscript received 9 November 1987, accepted 3 February 1988</em> Rhodium(I) carbonyl complexes of the type <em>trans</em>-[RhCl(CO)(R<sub>2</sub>SO/R<sub>2</sub>S)<sub>2</sub>], where R<sub>2</sub>SO=di-n-propyl sulphoxide (n-Pr<sub>2</sub>SO), di-n-butyl sulphoxide (n-Bu<sub>2</sub>SO) ; R<sub>2</sub>S= dimethyl sulphide (Me<sub>2</sub>S), di-isopropyl sulphide (i-Pr<sub>2</sub>S), undergo oxidative addition reactions with small covalent molecules (YZ) forming the adducts [RhClYZ(CO)- (R<sub>2</sub>SO/R<sub>2</sub>S)<sub>2
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36

Dalpozzo, Renato, and Raffaella Mancuso. "Enantioselective Vinylogous Reactions of 3-Alkylidene Oxindoles." Synthesis 50, no. 13 (2018): 2463–72. http://dx.doi.org/10.1055/s-0037-1609731.

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Oxindoles represent an important class of bioactive compounds and synthetic derivatives found in many natural products. Most of these compounds are chiral molecules and the challenge of their asymmetric synthesis has fascinated many research groups. In particular, the creation of chiral centers out of the oxindole ring by vinylogous addition to 3-alkylidene-substituted oxindoles (3-alkylidene-1,3-dihydro-2H-indol-2-ones) has emerged in recent years. This review aims to give an overview of this topic.1 Introduction2 Aldol and Mannich Reactions3 Addition to Unsaturated Carbonyl Compounds4 Additi
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37

Bao, Weiliang, Yunfa Zheng, and Yongmin Zhang. "Conjugate Addition of Organosamarium Reagents to Nitroalkenes." Journal of Chemical Research 23, no. 12 (1999): 732–33. http://dx.doi.org/10.1177/174751989902301224.

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38

Mathieu, Simon, and Georges Trinquier. "Oxidative addition of carbon dioxide into mesoionics." Physical Chemistry Chemical Physics 21, no. 10 (2019): 5531–65. http://dx.doi.org/10.1039/c8cp07321j.

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39

Peel, JB, and RG Rothwell. "C60 Framework Response to Halogen Addition: the Stable Isomers of C60Br2m." Australian Journal of Chemistry 47, no. 1 (1994): 131. http://dx.doi.org/10.1071/ch9940131.

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The isolation and spectroscopic characterization of halogenated fullerene-60 compounds has not advanced greatly during the 2 years of effort in this area. While the fully fluorinated C60F60 has been studied in some detail, other halogen addition processes have indicated chlorination up to C60Cl24 and bromination up to C60Br24. However, definitive structural information has to date only been provided for three compounds, namely C60Br6, C60Br6 and C60Br24. Iodine does not appear to form genuine addition compounds. In the work reported here semiempirical calculations using the AM1 approximation w
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40

Wilson, R. Marshall, Alvan C. Hengge, Ali Ataei, and Nuanphun Chantarasiri. "Addition of 4-phenyltriazolinedione to carbonyl compounds: the formation of .alpha.-urazolyl carbonyl compounds." Journal of Organic Chemistry 55, no. 1 (1990): 193–97. http://dx.doi.org/10.1021/jo00288a032.

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41

van der Veer, W., and F. Jellinek. "Adducts of thiophosphoryl compounds with metal halides. Part II: Addition compounds of thiophosphoryl chloride." Recueil des Travaux Chimiques des Pays-Bas 87, no. 4 (2010): 365–74. http://dx.doi.org/10.1002/recl.19680870403.

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42

Arslan, Recai, Ebru Karaçay, Derya Maraslıoğlu, et al. "Determination of the properties of medium-density fiberboards produced using urea-formaldehyde resins modified with boron compounds." BioResources 19, no. 3 (2024): 5367–83. http://dx.doi.org/10.15376/biores.19.3.5367-5383.

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Effects of adding different boron compounds to the urea-formaldehyde resin were evaluated relative to the physical, mechanical, and other properties of medium-density fiberboard (MDF). While the chemical addition of boric acid to the urea-formaldehyde resin increased the modulus of rupture and modulus of elasticity values of MDF boards, the physical and chemical additions of other boron compounds decreased those values. While there were no significant decreases in internal bond values, the chemical addition of boric acid and borax decahydrate to urea-formaldehyde resin increased the internal b
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43

Taşçı, Süleyman S., and Aslı Göksel. "Native Compounds in Turkish Sign Language (TİD): A classification based on headedness." Journal of Linguistics Research / Dilbilim Araştırmaları Dergisi 2018, no. 1 (2018): 1–28. https://doi.org/10.5281/zenodo.3765832.

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This paper investigates the position of the structural head and its connection to the semantic head in 127 compounds in Turkish Sign Language (TİD). To eliminate language contact effects, we selected compounds that have monomorphemic counterparts in Turkish. The findings are: (i) Endocentric compounds tend to be head-final, (ii) Exocentric compounds tend to be head-initial, (iii) compound internal order, in some well-defined cases, is affected by the lexical semantics of one of the components. In addition, we identify two classes of compounds, cranberry compounds and descriptive compounds, and
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44

Fujdala, Kyle L., David W. K. Gracey, Erica F. Wong, and Kim M. Baines. "The addition of organometallic reagents to tetramesityldigermene." Canadian Journal of Chemistry 80, no. 11 (2002): 1387–92. http://dx.doi.org/10.1139/v02-128.

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The thermolysis and photolysis of hexamesitylcyclotrigermane in the presence of ethylmagnesium bromide has been investigated. Under photochemical conditions, ethyldimesitylgermane, 1,2-diethyl-1,1,2-trimesityldigermane and ethyl-1,1,2,2-tetramesityldigermane were isolated and, under thermal conditions, 1,2,2-triethyl-1,1-dimesityl digermane and 2,2-diethyl-1,1,1-trimesityldigermane were isolated. The photolysis of hexamesitylcyclotrigermane in the presence of methyllithium has also been investigated. In both cases, the organometallic reagent adds to tetramesityl digermene and dimesitylgermylen
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45

Gombler, Willy, and Gerd Bollmann. "Reaktionen von CF3SF: Addition an C=S-Doppelbindungen / Reactions of CF3SF: Addition to C = S Double Bonds." Zeitschrift für Naturforschung B 47, no. 3 (1992): 369–72. http://dx.doi.org/10.1515/znb-1992-0311.

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AbstractTrifluoromethanesulfenylfluoride, CF3SF, adds to the carbon-sulfur double bond to form fluorinated compounds containing a trifluoromethyldisulfanyl group. Reactions of CF3SF with CS2,CF2S,CCl2S and (CF3S)2CS are described.
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46

TANAKA, Maski, Tomoaki IIJIMA, and Miyato HIGAKI. "Efect of addition of phenolic compounds on Chlorpyrifos degradation." Wood Preservation 20, no. 3 (1994): 125–28. http://dx.doi.org/10.5990/jwpa.20.125.

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47

Van Doorn, J. A., and R. L. Wife. "ADDITION OF DIPHENYLPHOSPHINE TO MALEIC ANHYDRIDE AND RELATED COMPOUNDS." Phosphorus, Sulfur, and Silicon and the Related Elements 47, no. 3-4 (1990): 253–60. http://dx.doi.org/10.1080/10426509008037976.

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48

Vinogradov, Maxim G., Alexander E. Kondorsky, and Gennady I. Nikishin. "Oxidative Addition of 1,3-Dicarbonyl Compounds to Conjugated Olefins." Synthesis 1988, no. 01 (1988): 60–62. http://dx.doi.org/10.1055/s-1988-27465.

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49

Hirao, Toshikazu, and Yoshiki Ohshiro. "Vanadium Dichloride Induced Addition of Bromotrichloromethane to Olefinic Compounds." Synlett 1990, no. 04 (1990): 217–18. http://dx.doi.org/10.1055/s-1990-21041.

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50

Nadeau, Frédéric, Michèle Sindt, and Nicolas Oget. "Free-solvent Michael addition of glycerol to acrylic compounds." New Journal of Chemistry 39, no. 12 (2015): 9155–61. http://dx.doi.org/10.1039/c5nj02223a.

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