Relevant bibliographies by topics / Butene-1(dimethyl-3,3)|ent

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Academic literature on the topic 'Butene-1(dimethyl-3,3)|ent'

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

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Journal articles on the topic "Butene-1(dimethyl-3,3)|ent"

1

Man, Wong Wee Choy Wong Chi, Hans Pritzkow, and Walter Siebert. "Notizen: Synthesis and Structure of a 2,4,5-Tris(methylene)-1-bora-3-silacyclopentane Derivative." Zeitschrift für Naturforschung B 46, no. 8 (1991): 1127–29. http://dx.doi.org/10.1515/znb-1991-0827.

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3,3-Dimethyl-(e)-1-chlorodimethylsilyl-1-chloro-dimethylaminoboryl-butene-1 (5) reacts with 3,4-dilithio-2,5-dimethyl-2,4-hexadiene in diethylether to give colorless 2-(tert-butylmethy-lene)-4,5-bis(dimethylmethylene)-1-dimethylamino-3-dimethyl-1-bora-3-sila-cyclopentane (4) in 41% yield. The X-ray structure analysis shows a non-planar ring with a small angle C2-Si3-C4 = 94.9(1)°.
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2

Crowder, G. A. "Interpretation of the vibrational spectra of 3,3‐dimethyl‐1‐butene." Journal of Environmental Science and Health . Part A: Environmental Science and Engineering and Toxicology 30, no. 7 (1995): 1457–71. http://dx.doi.org/10.1080/10934529509376278.

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3

Crowder, G. A. "Interpretation of the Vibrational Spectra Of 3,3-Dimethyl-1-Butene." Spectroscopy Letters 29, no. 1 (1996): 11–25. http://dx.doi.org/10.1080/00387019608001577.

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4

Wong-Chi-Man, Wong-Wee-Choy, Hans Pritzkow, and Walter Siebert. "Notizen: Synthesis and Structure of an 1,3-Dibora-2,5-disilacyclohexane Derivative." Zeitschrift für Naturforschung B 45, no. 11 (1990): 1597–99. http://dx.doi.org/10.1515/znb-1990-1124.

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Hydroboration, 3,3-Dimethyl-(e)-1-chlorodimethylsilyl-1-chloro-dimethylaminoboryl-butene-1,1,3-Bis(dimethylamino-2,2,5,5-tetramethyl-4,6-bis-(t-butylethylene)-1,3-dibora-2,5-disilacyclohexaneHydroboration of chlorodimethyl(3.3-dimethylbutynyl)silane with HBCl2/BCl3 yields 3.3-dimethyl-(e)-1-chlorodimethylsilyl-1-dichloroboryl)-butene-1 (1 a), in which a chlorine atom at the boron can be substituted using Me3SiNMe, to give the corresponding chlorodimethylaminoboryl derivative 1 b. Dehalogenation of 1 b with Na/K alloy does not lead to the three-membered ring compound 2, but surprisingly yields
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5

Bautista, F. M., J. M. Campelo, A. Garcia, et al. "Isomerization of 3,3-dimethyl-1-butene over aluminum and chromium orthophosphates." Reaction Kinetics and Catalysis Letters 64, no. 1 (1998): 41–48. http://dx.doi.org/10.1007/bf02475368.

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6

Katritzky, Alan R., Yunfeng Fang, and Indra Prakash. "ChemInform Abstract: A Novel Preparation of 3,3-Dimethylbutyraldehyde via Isomerization of 3,3-Dimethyl-1-butene Epoxide." ChemInform 33, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.200218091.

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7

Tuaillon, Jacques, Yvon Couture, and Jean Lessard. "Radical reactions of N-haloamides with olefins. XIII. Quantum yields for the photochemical addition of N-halo-N-hydroamides and N-chlorosuccinimide to 3,3-dimethyl-1-butene." Canadian Journal of Chemistry 65, no. 9 (1987): 2194–97. http://dx.doi.org/10.1139/v87-367.

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The quantum yield of the photochemically initiated radical chain addition of ZCONHX to 3,3-dimethyl-1-butene increases with Z in the order CH3 < ClCH2 < C2H5O < CCl3 < CF3 and is governed by the transfer step. The quantum yields are similar for N-chloroacetamide and N-chlorosuccinimide but the yield of addition is lower with the latter due to photodecomposition of the 1,2-adduct.
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8

Park, Jaebum, Jinhyung Lee, and Jaegab Lee. "Pulsed MOCVD of Cu Seed Layer Using a (hfac)Cu(3,3-dimethyl-1-butene) Source and H2Reactant." Korean Journal of Materials Research 14, no. 9 (2004): 619–26. http://dx.doi.org/10.3740/mrsk.2004.14.9.619.

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9

Deslauriers, Hélène, and Guy J. Collin. "The photolysis of 2,3- and 3,3-dimethyl-1-butene at 147.0 and 184.9 nm." Canadian Journal of Chemistry 63, no. 1 (1985): 62–67. http://dx.doi.org/10.1139/v85-011.

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The photofragmentation of 2,3-dimethylbutene and 3,3-dimethylbutene has been studied at 147 and 184.9 nm in the gas phase. The main primary decomposition process at both wavelengths involves the rupture of a β(C—C) bond. The quantum yield for this process is higher than 0.7 at 147 nm and is probably even higher at 184.9 nm. All dimethallyl radicals formed at 147 nm in this process decompose at low pressure, but some of them isomerize from the α,β- to the α,α- structure (and vice versa) — via a 1,4-H transfer — before decomposition. At 184.9 nm, the same primary process is used to get a rough v
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10

Nagaraja, C. M., Munirathinam Nethaji, and Balaji R. Jagirdar. "Tris(pyrazolyl)methane Sulfonate Complexes of Iridium: Catalytic Hydrogenation of 3,3-Dimethyl-1-butene." Organometallics 26, no. 25 (2007): 6307–11. http://dx.doi.org/10.1021/om700515n.

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