Relevant bibliographies by topics / 3-dimethylpentane / Journal articles
To see the other types of publications on this topic, follow the link: 3-dimethylpentane.

Journal articles on the topic '3-dimethylpentane'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 22 journal articles for your research on the topic '3-dimethylpentane.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Dokolas, Peter, Steven M. Loer, and David H. Solomon. "Reaction of Acyclic Hydrocarbons Towards t-Butoxy Radicals. A Study of Hydrogen Atom Abstraction by Using the Radical Trapping Technique." Australian Journal of Chemistry 51, no. 12 (1998): 1113. http://dx.doi.org/10.1071/c98055.

Full text
Abstract:
The reaction of 3-methylpentane and 2,4-dimethylpentane toward t-butoxy radicals has been investigated, in neat and benzene solutions, by using the radical trapping technique. Abstraction occurs principally from the tertiary and secondary C-H reaction sites of 3-methylpentane and the tertiary position of 2,4-dimethylpentane. The tertiary and in particular secondary C-H reaction sites of 2,4-dimethylpentane are shown to be considerably less susceptible towards t-butoxy radical facilitated abstraction compared with the equivalent reaction sites of 3-methylpentane. As a result, the latter is thre
APA, Harvard, Vancouver, ISO, and other styles
2

Svoboda, Václav, Vladimı́r Hynek, and Bohumı́r Koutek. "Enthalpies of vaporization, and the cohesive and internal energies of 2,2-dimethylpentane, 2,4-dimethylpentane, 2,2,3-trimethylpentane, 2,3,3-trimethylpentane, and 3-ethylpentane." Journal of Chemical Thermodynamics 30, no. 11 (1998): 1411–17. http://dx.doi.org/10.1006/jcht.1998.0414.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

NAGUMO, Shinji, Takayuki ARAI, and Hiroyuki AKITA. "Enzymatic Hydrolysis of meso(syn-syn)-1,3,5-Triacetoxy-2,4-dimethylpentane and Acetylation of meso(syn-syn)-3-Benzyloxy-2,4-dimethylpentane-1,5-diol by Lipase." CHEMICAL & PHARMACEUTICAL BULLETIN 44, no. 7 (1996): 1391–94. http://dx.doi.org/10.1248/cpb.44.1391.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

NAGUMO, S., T. ARAI, and H. AKITA. "ChemInform Abstract: Enzymatic Hydrolysis of meso(syn-syn)-1,3,5-Triacetoxy-2,4- dimethylpentane and Acetylation of meso(syn-syn)-3-Benzyloxy-2,4- dimethylpentane-1,5-diol by Lipase." ChemInform 28, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.199701051.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Solano-Serena, Floriane, Rémy Marchal, Serge Casarégola, Christelle Vasnier, Jean-Michel Lebeault, and Jean-Paul Vandecasteele. "A Mycobacterium Strain with Extended Capacities for Degradation of Gasoline Hydrocarbons." Applied and Environmental Microbiology 66, no. 6 (2000): 2392–99. http://dx.doi.org/10.1128/aem.66.6.2392-2399.2000.

Full text
Abstract:
ABSTRACT A bacterial strain (strain IFP 2173) was selected from a gasoline-polluted aquifer on the basis of its capacity to use 2,2,4-trimethylpentane (isooctane) as a sole carbon and energy source. This isolate, the first isolate with this capacity to be characterized, was identified by 16S ribosomal DNA analysis, and 100% sequence identity with a reference strain of Mycobacterium austroafricanum was found. Mycobacterium sp. strain IFP 2173 used an unusually wide spectrum of hydrocarbons as growth substrates, including n-alkanes and multimethyl-substituted isoalkanes with chains ranging from
APA, Harvard, Vancouver, ISO, and other styles
6

Schuler, Robert H., and Laszlo Wojnarovits. "Radical Yields in the Radiolysis of Branched Hydrocarbons: Tertiary C−H Bond Rupture in 2,3-Dimethylbutane, 2,4-Dimethylpentane, and 3-Ethylpentane." Journal of Physical Chemistry A 107, no. 43 (2003): 9240–47. http://dx.doi.org/10.1021/jp030658+.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Bouzas, Alberto, M. Cruz Burguet, Juan B. Montón, and Rosa Muñoz. "Densities, Viscosities, and Refractive Indices of the Binary Systems Methyltert-Butyl Ether + 2-Methylpentane, + 3-Methylpentane, + 2,3-Dimethylpentane, and + 2,2,4-Trimethylpentane at 298.15 K." Journal of Chemical & Engineering Data 45, no. 2 (2000): 331–33. http://dx.doi.org/10.1021/je9902793.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Guerrero-Zárate, David, Gustavo A. Iglesias-Silva та Alejandro Estrada-Baltazar. "P–ρ–T Data and Derivative Properties of 3-Methylpentane, 2,4-Dimethylpentane, and 2,3,4-Trimethylpentane from 283.15 to 363.15 K at Pressures up to 65 MPa". Journal of Chemical & Engineering Data 64, № 12 (2019): 6020–30. http://dx.doi.org/10.1021/acs.jced.9b00846.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Akai, Yuto, Laure Konnert, Takeshi Yamamoto, and Michinori Suginome. "Asymmetric Suzuki–Miyaura cross-coupling of 1-bromo-2-naphthoates using the helically chiral polymer ligand PQXphos." Chemical Communications 51, no. 33 (2015): 7211–14. http://dx.doi.org/10.1039/c5cc01074h.

Full text
Abstract:
Axially chiral 1,1′-biaryl-2-carboxylates were synthesized via Suzuki–Miyaura cross-coupling of 2,4-dimethylpentan-3-yl 1-halo-2-naphthoates with arylboronic acids with single-handed helical polymer ligands PQXphos.
APA, Harvard, Vancouver, ISO, and other styles
10

Collins, DJ, and HA Jacobs. "Steric and Stereoelectronic Effects in the Hydrogenolysis and Birch Reduction of Some Hindered Tertiary-Benzylic Carbinols." Australian Journal of Chemistry 40, no. 12 (1987): 1989. http://dx.doi.org/10.1071/ch9871989.

Full text
Abstract:
3-(4'-Methoxyphenyllpentan-3-ol (3a) and 3-(4'-methoxypheny1)-2,4-dimethylpentan-3-ol (3b) underwent catalytic hydrogenolysis over 10% palladium/charcoal at moderate temperatures and pressures. The more hindered tertiary-benzylic carbinols 3-(4'-methoxypheny1)-2,2,4-trimethylpentan-3-ol (6), 3-(4'-methoxyphenyl)-2,2,4,4-tetramethylpentan-3-ol (3c), 1-(4'- methoxyphenyl )-2,2,6,6-tetramethylcyclohexan-l-ol (8) and 1-(1',1'-dimethylethy1)-6-methoxy- 2,2-dimethyl-l,2,3,4-tetrahydronaphthalen-1-ol (10) were completely resistant to hydrogenolysis, even under vigorous conditions. While the hindered
APA, Harvard, Vancouver, ISO, and other styles
11

Wilson, W. C., J. Simon, and J. E. Garst. "The effects of selected bulky substituents on the pulmonary toxicity of 3-furyl ketones in mice." Journal of Animal Science 68, no. 4 (1990): 1072–76. http://dx.doi.org/10.2527/1990.6841072x.

Full text
Abstract:
Abstract Preliminary studies examined the toxicity of a series of simple alkyl 3-furyl ketone congeners of perilla ketone, 1-(3-furyl)-4-methylpentan-1-one (1), in mice, but little was known about how aromatic or bulky side chains might affect toxicity. Therefore, 3-furylphenyl ketone (2) 3-furylphenethyl ketone (3) and 1-3-furyl-4, 4-dimethylpentan-1-one (4) were synthesized to examine this problem. The 48-h LD50 (i.p.) in Notre Dame Swiss mice for each analog was greater than that of the parent toxicant, perilla ketone (1, 30 ± 5; 2, 173 ± 4; 3, 150 ± 11; 4, 79 ± 5 µmol/kg). Absorption and d
APA, Harvard, Vancouver, ISO, and other styles
12

Sharon, Daniel, Pessia Sharon, Daniel Hirshberg, et al. "2,4-Dimethoxy-2,4-dimethylpentan-3-one: An Aprotic Solvent Designed for Stability in Li–O2 Cells." Journal of the American Chemical Society 139, no. 34 (2017): 11690–93. http://dx.doi.org/10.1021/jacs.7b06414.

Full text
APA, Harvard, Vancouver, ISO, and other styles
13

Salzmann, Michael, Yuri P. Tsentalovich, and Hanns Fischer. "Photolysis of 2,4-dihydroxy-2,4-dimethylpentan-3-one studied by quantitative time-resolved CIDNP and optical spectroscopy." Journal of the Chemical Society, Perkin Transactions 2, no. 10 (1994): 2119. http://dx.doi.org/10.1039/p29940002119.

Full text
APA, Harvard, Vancouver, ISO, and other styles
14

Mills, Patrick L., and Ricky L. Fenton. "Vapor pressures, liquid densities, liquid heat capacities, and ideal gas thermodynamic properties for 3-methylhexanal and 3,4-dimethylpentanal." Journal of Chemical & Engineering Data 32, no. 2 (1987): 266–73. http://dx.doi.org/10.1021/je00048a035.

Full text
APA, Harvard, Vancouver, ISO, and other styles
15

Nguyen, Kim, Pascal Sutter, and Philip Kraft. "Search for New Linear Musks Devoid of a 2,2-Dimethyl-1,4-dioxa­butane Unit: Synthesis and Olfactory Properties of 5-Substituted (3E)-Hex-3-enoates on the Way to Carba-Helvetolide and Carba-Serenolide." Synthesis 49, no. 11 (2017): 2443–60. http://dx.doi.org/10.1055/s-0036-1588740.

Full text
Abstract:
Since the nucleophilic opening of isobutylene oxide competes with the formation of polyethers, the 2,2-dimethyl-1,4-dioxabutane moiety constitutes the most important cost driver in the synthesis of linear musks. Therefore, musk motifs devoid of this structural element would be highly attractive. Based on molecular modeling considerations, 5-methyl-substituted (3E)-configured alk-3-enoic esters accessible by deconjugative Knoevenagel reaction with malonic acid in the presence of piperidinium acetate with citronellal and Florhydral as substrates, were synthesized but showed disappointing olfacto
APA, Harvard, Vancouver, ISO, and other styles
16

Wibaut, J. P., and J. Smittenberg. "Comments on a paper by Paul L. Cramer and Verle A. Miller, entitled “The thermal decomposition of the acetate of 2,2-dimethylpentanol-3”)." Recueil des Travaux Chimiques des Pays-Bas 61, no. 5 (2010): 348–52. http://dx.doi.org/10.1002/recl.19420610504.

Full text
APA, Harvard, Vancouver, ISO, and other styles
17

Vakalopoulou, Efthymia, Christine Buchmaier, Andreas Pein, et al. "Synthesis and characterization of zinc di(O-2,2-dimethylpentan-3-yl dithiocarbonates) bearing pyridine or tetramethylethylenediamine coligands and investigation of their thermal conversion mechanisms towards nanocrystalline zinc sulfide." Dalton Transactions 49, no. 41 (2020): 14564–75. http://dx.doi.org/10.1039/d0dt03065a.

Full text
APA, Harvard, Vancouver, ISO, and other styles
18

Camara, Susana, Bruce C. Gilbert, Robert J. Meier, Martin van Duin, and Adrian C. Whitwood. "EPR and modelling studies of hydrogen-abstraction reactions relevant to polyolefin cross-linking and grafting chemistryElectronic supplementary information (ESI) available: computed 3D structures of the transition states of hydrogen abstraction from 2,4-dimethylpentane by tert-butoxyl radical. “1 ry24dmp.pdb”: H-abstraction from the methyl group (to generate a primary radical). “2ry24dmp.pdb”: H-abstraction from the central methylene group (to generate a secondary radical). “3 ry24dmp.pdb”: H-abstraction from the methine group (to generate a tertiary radical). See http://www.rsc.org/suppdata/ob/b2/b212543a/." Organic & Biomolecular Chemistry 1, no. 7 (2003): 1181–90. http://dx.doi.org/10.1039/b212543a.

Full text
APA, Harvard, Vancouver, ISO, and other styles
19

Valeev, R. F., G. R. Sunagatullina, V. V. Loza, and M. S. Miftakhov. "Synthesis of an Acyclic Precursor to Epothilone D Analog. Aldol Condensation of (1R)-1-(1,3-Dithiolan-2-yl)-1-(methoxymethoxy)- 2,2-dimethylpentan-3-one with C6‒C21 and C6‒C9 Aldehyde Segments." Russian Journal of Organic Chemistry 54, no. 10 (2018): 1548–52. http://dx.doi.org/10.1134/s1070428018100172.

Full text
APA, Harvard, Vancouver, ISO, and other styles
20

Khroyan, Taline V., Willma E. Polgar, Gerta Cami-Kobeci, Stephen M. Husbands, Nurulain T. Zaveri, and Lawrence Toll. "The First Universal Opioid Ligand, (2S)-2-[(5R,6R,7R,14S)-N-cyclopropylmethyl-4,5-epoxy-6,14-ethano-3-hydroxy-6-methoxymorphinan-7-yl]-3,3-dimethylpentan-2-ol (BU08028): Characterization of the In Vitro Profile and In Vivo Behavioral Effects in Mouse Models of Acute Pain and Cocaine-Induced Reward." Journal of Pharmacology and Experimental Therapeutics 336, no. 3 (2010): 952–61. http://dx.doi.org/10.1124/jpet.110.175620.

Full text
APA, Harvard, Vancouver, ISO, and other styles
21

Chen, Xiaoyu, Ruquan Liang, Lichun Wu, and Gan Cui. "Non-Equilibrium Molecular Dynamics Study of the Influence of Branching on the Soret Coefficient of Binary Mixtures of Heptane Isomers." Journal of Non-Equilibrium Thermodynamics, May 11, 2021. http://dx.doi.org/10.1515/jnet-2020-0110.

Full text
Abstract:
Abstract Equimolar mixtures composed of isomers were firstly used to investigate the molecular branching effect on thermal diffusion behavior, which was not disturbed by factors of molecular mass and composition in this work. Eight heptane isomers, including n-heptane, 2-methylhexane, 3-methylhexane, 2,2-dimethylpentane, 2,3-dimethylpentane, 2,4-dimethylpentane, 3,3-dimethylpentane and 3-ethylpentane, were chosen as the researched mixtures. A non-equilibrium molecular dynamics (NEMD) simulation with enhanced heat exchange (eHEX) algorithm was applied to calculate the Soret coefficient at T = 3
APA, Harvard, Vancouver, ISO, and other styles
22

Biswas, Suparna Mandal. "2-bromo-1-(2-hydroxyphenyI)-3,4-dimethyIpentan-1-one: A New Bromo-Compound with Stimulatory Activity Isolated from the Shed Leaves of Teak, (Tectona grandis L.)." Annals of Tropical Research, April 6, 2012, 65–78. http://dx.doi.org/10.32945/atr3414.2012.

Full text
Abstract:
A new Bromo isotopic compound has been isolated and purified from the Methanol Fraction of Teak leaves (MFTk). Chromatographic and spectral analyses (TLC, UV, MS, NMR, and IR) indicated the compound to be 2-bromo-1-(2-hydroxypheny1)-3, 4-dimethylpentan-1-one, in short, BrHPDMP with molecular weights 285 and 287. The whole leaf leachate of teak showed strong inhibitory activity in bioassay. But when fraction-4 (Methanolic fraction of teak leaf) was isolated and purified, it showed concentration dependent stimulatory activity on rice seeds. At 1000 ppm concentration, it showed 12.820% inhibition
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography