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Journal articles on the topic 'Butadienyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Bates, Gordon S., Michael D. Fryzuk, and Charles Stone. "Convenient synthesis and cycloaddition reactions of 2-phenylseleno-1,3-butadiene and 2-trialkylstannyl-1,3-butadienes." Canadian Journal of Chemistry 65, no. 11 (1987): 2612–17. http://dx.doi.org/10.1139/v87-431.

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The facile preparation of 2-trialkylstannyl-1,3-butadienes and 2-phenylseleno-1,3-butadiene by reaction of 2-(1,3-butadienyl)magnesium chloride with trialkylstannyl chlorides and phenylselenium chloride, respectively, is reported. The Diels–Alder reactivity of these dienes with a variety of activated dienophiles is also described. Finally, a novel transmetallation of tin, in vinyl stannanes, to selenium by use of phenylselenium chloride is outlined.

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2

Scattolin, Thomas, Fabiano Visentin, Claudio Santo, Valerio Bertolasi та Luciano Canovese. "The unexpected case of reactions of halogens and interhalogens with halide substituted Pd(ii) σ-butadienyl complexes". Dalton Transactions 45, № 28 (2016): 11560–67. http://dx.doi.org/10.1039/c6dt01964a.

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Palladium σ-butadienyl derivatives react with halogens and interhalogens, under mild experimental conditions, to induce the substitution of the halogen to coordinated palladium and to the terminal butadienyl carbon without extrusion of the butadienyl fragment.

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3

Brisdon, Brian J., and Richard A. Walton. "Transition metal butadienyl complexes." Polyhedron 14, no. 10 (1995): 1259–76. http://dx.doi.org/10.1016/0277-5387(95)00060-6.

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4

Gromov, S. P., S. A. Sergeev, S. I. Druzhinin, et al. "Crown-containing butadienyl dyes." Russian Chemical Bulletin 48, no. 3 (1999): 525–36. http://dx.doi.org/10.1007/bf02496174.

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5

Zhang, Wen-Xiong, and Zhenfeng Xi. "1-Lithio-1,3-dienes as useful building blocks in organic synthesis." Pure and Applied Chemistry 81, no. 2 (2009): 235–46. http://dx.doi.org/10.1351/pac-con-08-08-04.

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Both intermolecular reactivities toward C-O and C-N unsaturated substrates and intramolecular reactions of various 1-lithio-1,3-dienes are briefly summarized. Results reveal that intramolecular synergy between the alkenyllithium moiety and the butadienyl skeleton make 1-lithio-1,3-diene derivatives useful and unique as building blocks in organic synthesis. It is demonstrated that substitution patterns and the nature of the substituents on the butadienyl skeleton have remarkable effects on reaction pathways.

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6

Settambolo, Roberta. "Synthesis of 3-Butadienyl-1-tosylpyrroles." Journal of Heterocyclic Chemistry 52, no. 3 (2014): 896–901. http://dx.doi.org/10.1002/jhet.2155.

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7

Fan, Yueqian, Juan Chen, Le Yu, et al. "Methyl substitution enhanced photoisomerization of trans,trans-1,4-diphenyl-1,3-butadiene: direct ab initio trajectory surface hopping dynamic simulations." Physical Chemistry Chemical Physics 20, no. 4 (2018): 2260–73. http://dx.doi.org/10.1039/c7cp07465d.

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8

Xie, Yi-Wen, Zhen-Ni Zhao, Zi-Wei Lin, Yu-Hao Wang, Ya-Qun Liu та Yi-Yong Huang. "Asymmetric Petasis reaction for the synthesis of chiral α- and β-butadienyl amines". Chemical Communications 57, № 19 (2021): 2364–67. http://dx.doi.org/10.1039/d0cc08241d.

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9

Canovese, Luciano, Fabiano Visentin, Thomas Scattolin, Claudio Santo, and Valerio Bertolasi. "The addition of bromine and iodine to palladacyclopentadienyl complexes bearing bidentate heteroditopic P−N spectator ligands derived from differently substituted quinolinic frames. The unexpected evolution of the reaction." Dalton Transactions 44, no. 33 (2015): 15049–58. http://dx.doi.org/10.1039/c5dt01884f.

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10

Sierra, C. A., C. Galán, J. M. Gómez Fatou, and V. Ruíz Santa Quiteria. "Dynamic-Mechanical Properties of Tin-Coupled SBRs." Rubber Chemistry and Technology 68, no. 2 (1995): 259–66. http://dx.doi.org/10.5254/1.3538740.

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Abstract The interaction between rubber and carbon black in compounds for road tire treads has been analyzed by using mechanical and dynamical measurements in three cured compounds based on SBRs. The rubbers were prepared in solution by anionic polymerization, and coupled with tin compounds in which the carbon-tin bond at the end of the chain may correspond to styryl or butadienyl terminations. The interaction parameter, defined by the ratio of mechanical and dynamic terms, has been used for the first time for the evaluation of the compounds. The SBRs with tin-butadienyl bonds exhibit an impro

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11

Bains, Deepak, Yogesh Kumar, Prabhpreet Singh, and Gaurav Bhargava. "[2 + 2] Cycloaddition Reactions of Butadienyl Ketene with 1,4-Diazabuta-1,3-dienes: Synthesis of Functionalized Butadienyl-4-iminomethyl-azetidin-2-ones and Butenylidene-butadienyl-[2,2′-biazetidine]-4,4′-diones." Journal of Heterocyclic Chemistry 53, no. 5 (2015): 1665–69. http://dx.doi.org/10.1002/jhet.2465.

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12

Sergeeva, T. I., S. Yu Zaitsev, M. S. Tsarkova, et al. "Monolayers of a novel ionoselective butadienyl dye." Journal of Colloid and Interface Science 265, no. 1 (2003): 77–82. http://dx.doi.org/10.1016/s0021-9797(03)00051-1.

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13

Chou, Ta Shue, Su Chun Hung, and Hsi Hwa Tso. "4-Bromo-2-sulfolenes. Butadienyl cation equivalents." Journal of Organic Chemistry 52, no. 15 (1987): 3394–99. http://dx.doi.org/10.1021/jo00391a042.

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14

Ushakov, E. N., S. P. Gromov, L. G. Kuz"mina, et al. "Crown-containing butadienyl dyes. 5. Structure and photoisomerization of a butadienyl dye containing a 15-crown-5 fragment." Russian Chemical Bulletin 53, no. 7 (2004): 1549–62. http://dx.doi.org/10.1023/b:rucb.0000046254.69634.50.

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15

Schubert, Hans, and Manfred Regitz. "1-(1,3-Butadienyl)triazole aus 1-Vinyltriazolen und elektronenreichen Alkinen - Spaltung zu „push pull”︁-1,3-Butadienen." Angewandte Chemie 95, no. 7 (2006): 564. http://dx.doi.org/10.1002/ange.19830950716.

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16

Dennett, James N. L., Selby A. R. Knox, Jonathan P. H. Charmant, Amy L. Gillon та A. Guy Orpen. "Synthesis and reactivity of μ-butadienyl diruthenium cations". Inorganica Chimica Acta 354 (жовтень 2003): 29–40. http://dx.doi.org/10.1016/s0020-1693(03)00391-8.

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17

Krivykh, Vasily V., та Ivan V. Glukhov. "Cationic η3-butadienyl complexes of chromium and manganese". Mendeleev Communications 20, № 3 (2010): 177–79. http://dx.doi.org/10.1016/j.mencom.2010.05.019.

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18

Nagano, Noriaki, Hirotsune Itahana, Hiroyuki Hisamichi, Kenichiro Sakamoto, and Ryuichiro Hara. "A facile synthesis of 3-(1,3-butadienyl)cephalosporins." Tetrahedron Letters 35, no. 26 (1994): 4577–78. http://dx.doi.org/10.1016/s0040-4039(00)60733-5.

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19

Gökmen, Zeliha. "New Heterocyclic Compounds From Butadienyl Sulfanes and Thiols." Asian Journal of Chemistry 26, no. 4 (2014): 991–96. http://dx.doi.org/10.14233/ajchem.2014.15720.

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20

Angelov, Christo M., Johan P. van den Heever, Robert McDonald, Alexander J. B. McEwan, and John R. Mercer. "Anilinium 3-methyl-1,2-butadienyl-1,1-diphosphonate(1–)." Acta Crystallographica Section E Structure Reports Online 58, no. 5 (2002): o498—o500. http://dx.doi.org/10.1107/s1600536802005743.

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21

Park, Hea Jung, Jung Soo Seo, Dae Won Cho, and Ung Chan Yoon. "Photoadditions of Silyl Butadienyl Ether to 1,2-Diketones." Journal of the Korean Chemical Society 57, no. 1 (2013): 9–11. http://dx.doi.org/10.5012/jkcs.2013.57.1.9.

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22

Xi, Zhenfeng, Wenxiong Zhang, and Tamotsu Takahashi. "Selective preparation of 1,3-butadienyl phosphines, 1-iodo- and 1,4-diiodo-butadienyl phosphine oxides via zirconocene-mediated cross-coupling of alkynylphosphines." Tetrahedron Letters 45, no. 11 (2004): 2427–29. http://dx.doi.org/10.1016/j.tetlet.2004.01.098.

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23

Porfiriev, Denis P., Valeriy N. Azyazov, and Alexander M. Mebel. "Mechanism and kinetics of the oxidation of 1,3-butadien-1-yl (n-C4H5): a theoretical study." Physical Chemistry Chemical Physics 23, no. 15 (2021): 9198–210. http://dx.doi.org/10.1039/d1cp00567g.

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According to ab initio calculations of the potential energy surface combined with RRKM-ME calculations of rate constants and product branching ratios, the n-C<sub>4</sub>H<sub>5</sub> + O<sub>2</sub> reaction mostly produces 1-oxo-n-butadienyl + O and acrolein + HCO.

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24

Hodson, Annabelle G. W., та Rupinder K. Thind. "Stereochemistry of chiral, substituted η3-butadienyl molybdenum(II) complexes". Polyhedron 19, № 7 (2000): 791–99. http://dx.doi.org/10.1016/s0277-5387(00)00315-6.

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25

Teulade, Marie-Paule, and Philippe Savignac. "A general one-pot synthesis of 1,3-butadienyl phosphanes." Tetrahedron Letters 30, no. 46 (1989): 6327–30. http://dx.doi.org/10.1016/s0040-4039(01)93884-5.

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26

Parker, C. L., and A. L. Cooksy. "Ab Initio Study of the 1,3-butadienyl Radical Isomers." Journal of Physical Chemistry A 102, no. 30 (1998): 6186–90. http://dx.doi.org/10.1021/jp980970x.

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27

Angelov, Christo M., Dean A. Mazzuca, Johan P. van den Heever, Robert McDonald, Alexander J. B. McEwen, and John R. Mercer. "2-(3-Methyl-1,2-butadienyl)-2-oxo-1,3,2-oxazaphosphorinane." Acta Crystallographica Section E Structure Reports Online 58, no. 4 (2002): o399—o401. http://dx.doi.org/10.1107/s1600536802004105.

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28

de Visser, Sam P., Leo J. de Koning, Wim J. van der Hart, and Nico M. M. Nibbering. "Chemical properties of butadienyl anions in the gas-phase." Recueil des Travaux Chimiques des Pays-Bas 114, no. 6 (2010): 267–72. http://dx.doi.org/10.1002/recl.19951140603.

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29

Slugovc, Christian, Kurt Mereiter, Roland Schmid та Karl Kirchner. "Cross Coupling of Acetylenes with Olefins – Formation of η3-Butadienyl and η2-Butadiene Complexes via a Metallacyclobutane Intermediate". European Journal of Inorganic Chemistry 1999, № 7 (1999): 1141–49. http://dx.doi.org/10.1002/(sici)1099-0682(199907)1999:7<1141::aid-ejic1141>3.0.co;2-4.

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30

Meagher, Timothy P., Larry Yet, Chi-Nung Hsiao, and Harold Shechter. "(E)- and (Z)-1-(Phenylsulfonyl)-4-(trimethylsilyl)-2-butenes: Synthetic Equivalents for the 1-(1,3-Butadienyl) Anion and the 1,1-(1,3-Butadienyl) Dianion." Journal of Organic Chemistry 63, no. 13 (1998): 4181–92. http://dx.doi.org/10.1021/jo970545k.

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31

Meagher, Timothy P., and Harold Shechter. "(E)-1-(Phenylsulfonyl)-4-(trimethylsilyl)-1-butene: An Advantageous Synthetic Equivalent for the 1-(1,3-Butadienyl) Anion and the 1,1-(1,3-Butadienyl) Dianion." Journal of Organic Chemistry 63, no. 13 (1998): 4193–98. http://dx.doi.org/10.1021/jo970546c.

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32

Collin, Guy J., Hélène Deslauriers, and George R. De Maré. "La photochimie du cis-penta-1,3-diène, en phase gazeuse à 184,9 et 147,0 nm." Canadian Journal of Chemistry 69, no. 8 (1991): 1245–51. http://dx.doi.org/10.1139/v91-186.

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We have studied the 184.9 and 147.0 nm photochemistry of gaseous cw-1,3-pentadiene: the main products observed at 184.9 nm are trans-1,3-pentadiene and 1,3-cyclopentadiene. The formation of radicals also occurs as shown through the use of DI as a radical scavenger. Cyclopentadiene is the likely product of successive eliminations of two hydrogen atoms from the photoexcited molecule after rearrangement of the pentadienyl radical to the cyclopentenyl structure: Ф0(cyclo-C5H6) ≈ 0.25. Elimination of a methyl radical (Ф0 ≈ 0.50) also occurs, with formation of CH2=CHCH=ĊH* and, in a lower yield, CH2

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33

De Cusati, Paul F., and R. A. Olofson. "A simple synthesis of 1-(1,3-butadienyl) carbonates and carbamates." Tetrahedron Letters 31, no. 10 (1990): 1405–8. http://dx.doi.org/10.1016/s0040-4039(00)88817-6.

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34

Reglier, Marius, та Sylvestre A. Julia. "Stereospecific cyclisations of substituted α′-lithiatedα(Z), γ-butadienyl sulfoxides". Tetrahedron Letters 26, № 22 (1985): 2655–58. http://dx.doi.org/10.1016/s0040-4039(00)98128-0.

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35

Yadva, J. S., D. Srinivas, and T. Shekharam. "An expeditious approach to the synthesis of chiral butadienyl alcohols." Tetrahedron Letters 35, no. 21 (1994): 3625–28. http://dx.doi.org/10.1016/s0040-4039(00)73257-6.

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36

Jasinski, Jerry P., John M. Jasinski, and Daniel J. Crosby. "2-{4-[4-(Dimethylamino)phenyl]-1,3-butadienyl}-1-ethylpyridinium perchlorate." Acta Crystallographica Section E Structure Reports Online 58, no. 11 (2002): o1283—o1284. http://dx.doi.org/10.1107/s1600536802019013.

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37

Zaitsev, Sergei Yu, Tatjana I. Sergeeva, Dietmar Möbius, et al. "Synthesis and ion-selective properties of an amphiphilic butadienyl dye." Mendeleev Communications 14, no. 5 (2004): 199–200. http://dx.doi.org/10.1070/mc2004v014n05abeh001923.

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38

Gómez, Ana M., J. Cristóbal López, and Bert Fraser-Reid. "A Convenient, Short Synthesis of (E)-1,3-Butadienyl(tributyl)stannane." Synthesis 1993, no. 10 (1993): 943–44. http://dx.doi.org/10.1055/s-1993-25971.

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39

Brinker, Udo H., and Ilona Fleischhauer. "Carben-Umlagerungen, XX.trans-2-(1,3-Butadienyl)cyclopropyliden: Erzeugung und Umlagerungsverhalten." Chemische Berichte 119, no. 4 (1986): 1244–68. http://dx.doi.org/10.1002/cber.19861190414.

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40

NAGANO, N., H. ITAHANA, H. HISAMICHI, K. SAKAMOTO, and R. HARA. "ChemInform Abstract: A Facile Synthesis of 3-(1,3-butadienyl)cephalosporins." ChemInform 25, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.199446262.

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41

Yongskulrote, Warunee, J. Morris Bramlett, Carl A. Mike, Bill Durham, and Neil T. Allison. "Photochemical conversion of (.eta.1-butadienyl)iron complexes to hydroxyferrocenes." Organometallics 8, no. 2 (1989): 556–58. http://dx.doi.org/10.1021/om00104a045.

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42

Bhargava, Gaurav, Maninderjeet K. Mann та Rayees Ahmad Naikoo. "3-Butadienyl-β-lactams: A useful synthon for functionalized heterocycles". Synthetic Communications 50, № 24 (2020): 3757–76. http://dx.doi.org/10.1080/00397911.2020.1813778.

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43

Herberich, Gerhard E., and Horst Mayer. "Niobocene chemistry: acetylene hydrido, acetylene alkenyl, and carbenoid butadienyl complexes." Organometallics 9, no. 10 (1990): 2655–61. http://dx.doi.org/10.1021/om00160a011.

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44

Bianchini, Claudio, M. Victoria Jimenez, Andrea Meli, and Francesco Vizza. "Rhodium-Assisted Transformations of Substituted Thiophenes into Butadienyl Methyl Sulfides." Organometallics 14, no. 10 (1995): 4858–64. http://dx.doi.org/10.1021/om00010a056.

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45

Benyunes, Stephen A., Lutz Brandt, Michael Green, and Adrian W. Parkins. "Synthesis and reactivity of cationic (.eta.3-butadienyl)platinum complexes." Organometallics 10, no. 1 (1991): 57–59. http://dx.doi.org/10.1021/om00047a029.

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46

Franz, Andreas, Pierre-Yves Eschler, Manuel Tharin, Helen Stoeckli-Evans, and Reinhard Neier. "Preparation of N-Alkylketene-N-Butadienyl-N,O-Silyl Acetals." Synthesis 1996, no. 10 (1996): 1239–45. http://dx.doi.org/10.1055/s-1996-4359.

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47

Dulcère, Jean-Pierre, Estelle Dumez та Robert Faure. "Preparation of 3-Butadienyl Tetrahydrofurans and α-Butadienyl γ-Butyrolactones by Radical Cyclization of β-Bromopent-4-en-2-ynyl Ethers and mixed Acetals". Synlett 1996, № 04 (1996): 391–92. http://dx.doi.org/10.1055/s-1996-5405.

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48

MEAGHER, T. P., and H. SHECHTER. "ChemInform Abstract: (E)-1-(Phenylsulfonyl)-4-(trimethylsilyl)-1-butene: An Advantageous Synthetic Equivalent for the 1-(1,3-Butadienyl) Anion and the 1,1-(1,3-Butadienyl) Dianion." ChemInform 29, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199844069.

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49

MEAGHER, T. P., L. YET, C. N. HSIAO, and H. SHECHTER. "ChemInform Abstract: (E)- and (Z)-1-(Phenylsulfonyl)-4-(trimethylsilyl)-2-butenes: Synthetic Equivalents for the 1-(1,3-Butadienyl) Anion and the 1,1-(1,3-Butadienyl) Dianion." ChemInform 29, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199845079.

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50

Anaç, Olcay, and Füsun Şeyma Güngör. "Electrocyclization reactions of vinyl, styryl, and butadienyl conjugated carbonyl/azomethine ylides." Tetrahedron 66, no. 32 (2010): 5931–53. http://dx.doi.org/10.1016/j.tet.2010.05.058.

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