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Journal articles on the topic 'Aliphatic compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Gordon, P. F. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 82 (1985): 109. http://dx.doi.org/10.1039/oc9858200109.

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2

Gordon, P. F. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 83 (1986): 99. http://dx.doi.org/10.1039/oc9868300099.

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3

Gordon, P. F. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 84 (1987): 113. http://dx.doi.org/10.1039/oc9878400113.

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4

Smith, B. V. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 85 (1988): 105. http://dx.doi.org/10.1039/oc9888500105.

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5

Smith, B. V. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 86 (1989): 103. http://dx.doi.org/10.1039/oc9898600103.

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6

Smith, B. V. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 87 (1990): 117. http://dx.doi.org/10.1039/oc9908700117.

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7

SMITH, B. V. "ChemInform Abstract: Aliphatic Compounds. Part 2. Other Aliphatic Compounds." ChemInform 23, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199216336.

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8

SMITH, B. V. "ChemInform Abstract: Aliphatic Compounds. Part 2. Other Aliphatic Compounds." ChemInform 25, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.199403258.

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9

Yates, Peter, and J. A. Eenkhorn. "Aliphatic diazo compounds." Tetrahedron 44, no. 11 (1988): 3159–70. http://dx.doi.org/10.1016/s0040-4020(01)85947-0.

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10

SINGH, RS, RAHUL SINHA, and DEEPAK KUMAR SINGH. "Two new aliphatic compounds from the medicinal herb Crinum defixum." Journal of Medicinal and Aromatic Plant Sciences 35, no. 2013 (2013): 142–46. http://dx.doi.org/10.62029/jmaps.v35i3.singh.

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Two new aliphatic compounds namely 32-hydroxyheptatetracontan-21, 24-dione (A2) and oc tacosan-7, 19-di ol (A3) along with hentriacontane (A1) have been isolated from the hexane soluble extract of the shoots of the medicinal plant Crinum defixum. The structures of the compounds were elucidated on the basis of spectral and chemical studies.

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11

Baranov, G. M., and V. V. Perekalin. "Aliphatic organophosphorus nitro-compounds." Russian Chemical Reviews 61, no. 12 (1992): 1220–37. http://dx.doi.org/10.1070/rc1992v061n12abeh001027.

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12

Dinel, H., M. Lévesque, and P. Jambu. "Effects of long-chain aliphatic compounds on the germination and initial growth of corn, radish and spinach seedlings, and on hydrological properties of a sand growth medium." Canadian Journal of Soil Science 72, no. 2 (1992): 107–12. http://dx.doi.org/10.4141/cjss92-010.

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A greenhouse and laboratory study was carried out to determine the effects of various amounts (0.5–2.0%) of long-chain aliphatic compounds (LCA) of beeswax on the germination and initial growth (25 d) of corn, radish and spinach seedlings, and on the hydraulic properties of the sand growth medium. Complete emergence was obtained for corn, irrespective of aliphatic addition, whereas, the germination rate of the other two species decreased gradually as the amount of aliphatics added increased. With 2% LCA, 40 and 60%, respectively, of radish and spinach seeds failed to germinate. Dry matter yiel

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13

ONO, Noboru, Hideyoshi MIYAKE, and Aritsune KAJI. "Denitrohydrogenation of aliphatic nitro compounds." Journal of Synthetic Organic Chemistry, Japan 43, no. 2 (1985): 121–32. http://dx.doi.org/10.5059/yukigoseikyokaishi.43.121.

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14

Bouillon, Jean-Philippe, Christian Maliverney, Robert Merényi, and Heinz G. Viehe. "Trifluoromethylation of aliphatic halogen compounds." J. Chem. Soc., Perkin Trans. 1, no. 9 (1991): 2147–49. http://dx.doi.org/10.1039/p19910002147.

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15

Leisinger, Thomas. "Biodegradation of chlorinated aliphatic compounds." Current Opinion in Biotechnology 7, no. 3 (1996): 295–300. http://dx.doi.org/10.1016/s0958-1669(96)80033-4.

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16

Kempa, S., L. Wallach, and K. Rueck-Braun. "ChemInform Abstract: Aliphatic Azo Compounds." ChemInform 43, no. 36 (2012): no. http://dx.doi.org/10.1002/chin.201236234.

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17

ADOLPH, H. G., and W. M. KOPPES. "ChemInform Abstract: Aliphatic Fluoronitro Compounds." ChemInform 22, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199136291.

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18

B., DINDA, та K. SARA M. "Aliphatic Compounds from Melαstomα melαbαthricum". Journal of Indian Chemical Society Vol. 63, Aug 1986 (1986): 764–66. https://doi.org/10.5281/zenodo.6297402.

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Department of Chemistry, Calcutta University Post Graduate Centre, Agartala-799 004 <em>Manuscript received 31 July 1985, revised 3 February 1986, accepted 2 August 1986</em> Two new aliphatic compounds, 1-octyl docosanoate and 11-metbyl-1-tritriacontanol have been isolated from the aerial parts of <em>Melαstomα melαbαthricum</em> and characterised on the basis of chemical and spectroscopic evidences.  

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19

Pattison, Graham. "Fluorination of organoboron compounds." Organic & Biomolecular Chemistry 17, no. 23 (2019): 5651–60. http://dx.doi.org/10.1039/c9ob00832b.

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20

Xing, Li-Juan, Xi-Mei Wang, Hong-Ying Li, et al. "Metal-free synthesis of methylene-bridged bis-1,3-dicarbonyl compounds via oxidative C–C bond cleavage of tertiary aliphatic amines." RSC Adv. 4, no. 51 (2014): 26783–86. http://dx.doi.org/10.1039/c4ra04419c.

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A metal-free Bu<sub>4</sub>NI mediated oxidative reaction utilizing tertiary aliphatic amines and 1,3-dicarbonyl compounds for the synthesis of methylene-bridged bis-1,3-dicarbonyl compounds has been developed. This reaction involved an unexpected C–C bond cleavage of tertiary aliphatic amines.

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21

Chortyk, O. T., I. E. Yates, and C. C. Reilly. "Changes in Cuticular Compounds of Developing Pecan Leaves." Journal of the American Society for Horticultural Science 120, no. 2 (1995): 329–35. http://dx.doi.org/10.21273/jashs.120.2.329.

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Leaf surface compounds of pecan [Carya illinoensis (Wangenh.) C. Koch] were analyzed with regard to developmental stage and to susceptibility to infection by Cladosporium caryigenum (Ell. et Lang. Gottwald). Immature and mature leaves of two resistant (`Elliott' and `Sumner') and two susceptible (`Wichita' and `Schley') cultivars were extracted with methylene chloride. Extracts were separated by silicic acid chromatography into polar and nonpolar fractions. Constituents of each fraction were subsequently separated by gas chromatography and were identified by gas chromatography-mass spectroscop

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22

LI, XIAO-HONG, GENG-XIN YIN, and XIAN-ZHOU ZHANG. "THEORETICAL STUDIES ON BOND DISSOCIATION ENERGIES FOR SOME ALIPHATIC ALCOHOL COMPOUNDS BY DENSITY FUNCTIONAL THEORY AND CBS-Q METHOD." Journal of Theoretical and Computational Chemistry 10, no. 02 (2011): 179–89. http://dx.doi.org/10.1142/s0219633611006335.

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Quantum chemical calculations are used to estimate the bond dissociation energies (BDEs) for 20 aliphatic alcohol compounds. These compounds are studied by employing the hybrid density functional theory (B3LYP, B3PW91, and B3P86) methods with 6-311G** basis set and the complete basis set (CBS-Q) method together. It is demonstrated that B3P86 and CBS-Q methods are accurate to compute the reliable BDEs for aliphatic alcohol compounds. In order to test whether the non-local BLYP method suggested by Jursic18 is general for our study and whether B3P86 method has a low basis set sensitivity, the BDE

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23

Alcántara, María-Paz Derri, Francisca Cabrera Escribano, Antonio Gómez-Sánchez, et al. "Synthesis of Aliphatic 1,3-Dinitro Compounds." Synthesis 1996, no. 01 (1996): 64–70. http://dx.doi.org/10.1055/s-1996-4150.

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24

Feikus, Martin, and Peter H. Laur. "New Aliphatic Tellurenyl and Tellurinyl Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 67, no. 1-4 (1992): 73–78. http://dx.doi.org/10.1080/10426509208045821.

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25

Sobenina, Lyubov N., Albina I. Mikhaleva, and Boris A. Trofimov. "Synthesis of pyrroles from aliphatic compounds." Russian Chemical Reviews 58, no. 2 (1989): 163–80. http://dx.doi.org/10.1070/rc1989v058n02abeh003433.

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26

Nazin, Gennadii M., and Georgii B. Manelis. "Thermal decomposition of aliphatic nitro-compounds." Russian Chemical Reviews 63, no. 4 (1994): 313–22. http://dx.doi.org/10.1070/rc1994v063n04abeh000086.

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27

Nakatani, Munehiro, Yuji Fukunaga, and Tsunao Hase. "Aliphatic compounds from Hybiscus rosa-sinensis." Phytochemistry 25, no. 2 (1986): 449–52. http://dx.doi.org/10.1016/s0031-9422(00)85499-0.

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28

YAGI, OSAMI, and KAZUHIRO IWASAKI. "Biodegradation of Volatile Aliphatic Chlorinated Compounds." Microbes and environments 13, no. 3 (1998): 165–70. http://dx.doi.org/10.1264/jsme2.13.165.

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29

Holubowitch, Nicolas, Zachary Budimir, and Cameo Crabtree. "Spectroelectrochemistry of Explosive Aliphatic Nitro Compounds." ECS Meeting Abstracts MA2020-01, no. 45 (2020): 2565. http://dx.doi.org/10.1149/ma2020-01452565mtgabs.

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30

Misra, Triguna N., Ram S. Singh, and Hari S. Pandey. "Aliphatic compounds from Adenocalymma alliaceum leaves." Phytochemistry 30, no. 2 (1991): 541–43. http://dx.doi.org/10.1016/0031-9422(91)83723-x.

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31

Benn, M. "Aliphatic nitro-compounds in Astragalus canadensis." Phytochemistry 40, no. 6 (1995): 1629–31. http://dx.doi.org/10.1016/0031-9422(95)00482-m.

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32

Apasov, �. T., A. V. Kalinin, Yu A. Strelenko, and V. A. Tartakovskii. "New reaction of aliphatic nitro compounds." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 12 (1988): 2594–95. http://dx.doi.org/10.1007/bf00952656.

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33

Ono, Noboru, Hideyoshi Miyake, Akio Kamimura, Isami Hamamoto, Rui Tamura, and Aritsune Kaji. "Denitrohydrogenation of aliphatic nitro compounds and a new use of aliphatic nitro compounds as radical precursors." Tetrahedron 41, no. 19 (1985): 4013–23. http://dx.doi.org/10.1016/s0040-4020(01)97180-7.

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34

Ryu, Jaihyunk, Jae Il Lyu, Dong-Gun Kim, et al. "Comparative Analysis of Volatile Compounds of Gamma-Irradiated Mutants of Rose (Rosa hybrida)." Plants 9, no. 9 (2020): 1221. http://dx.doi.org/10.3390/plants9091221.

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Roses are one of the most important floricultural crops, and their essential oils have long been used for cosmetics and aromatherapy. We investigated the volatile compound compositions of 12 flower-color mutant variants and their original cultivars. Twelve rose mutant genotypes were developed by treatment with 70 Gy of 60Co gamma irradiation of six commercial rose cultivars. Essential oils from the flowers of the 18 genotypes were analyzed by gas chromatography–mass spectrometry. Seventy-seven volatile compounds were detected, which were categorized into six classes: Aliphatic hydrocarbons, al

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35

Bhawar, Ramesh, Kiran S. Patil, and Shubhankar Kumar Bose. "CeO2–nanocubes as efficient and selective catalysts for the hydroboration of carbonyl groups." New Journal of Chemistry 45, no. 33 (2021): 15028–34. http://dx.doi.org/10.1039/d1nj00065a.

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An efficient and reusable CeO2 nanocatalyst has been developed for the selective hydroboration of carbonyl compounds, including aromatic, heteroaromatic, aliphatic, and (hetero)aliphatic aldehydes and ketones.

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36

April, T. M., J. M. Foght, and R. S. Currah. "Hydrocarbon-degrading filamentous fungi isolated from flare pit soils in northern and western Canada." Canadian Journal of Microbiology 46, no. 1 (1999): 38–49. http://dx.doi.org/10.1139/w99-117.

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Sixty-four species of filamentous fungi from five flare pits in northern and western Canada were tested for their ability to degrade crude oil using gas chromatographic analysis of residual hydrocarbons following incubation. Nine isolates were tested further using radiorespirometry to determine the extent of mineralization of model radiolabelled aliphatic and aromatic hydrocarbons dissolved in crude oil. Hydrocarbon biodegradation capability was observed in species representing six orders of the Ascomycota. Gas chromatography indicated that species capable of hydrocarbon degradation attacked c

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37

Mitkov, Javor, Nikolai Danchev, Irina Nikolova, and Alexander Zlatkov. "Synthesis and brain antihypoxic activity of some aliphatic and arylaliphatic amides of caffeine-8-thioglycolic acid." Acta Pharmaceutica 57, no. 3 (2007): 361–70. http://dx.doi.org/10.2478/v10007-007-0029-1.

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Synthesis and brain antihypoxic activity of some aliphatic and arylaliphatic amides of caffeine-8-thioglycolic acidThe synthesis of some aliphatic and arylaliphatic amides of caffeine-8-thioglycolic acid was studied. The structures of synthesized compounds were proved by micro-analyses, IR- and1H NMR data. Values of acutep.o.andi.p.toxicity in mice show lower toxicity compared to caffeine. Declines in spontaneous locomotor activity support the idea of depressive CNS activity of the compounds. Two compounds exhibited brain antihypoxic activity (5aand5bagainst haemic and circulatory hypoxia, res

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38

Gui, Jingjing, Xin Cai, Lingyun Chen, et al. "Facile and practical hydrodehalogenations of organic halides enabled by calcium hydride and palladium chloride." Organic Chemistry Frontiers 8, no. 17 (2021): 4685–92. http://dx.doi.org/10.1039/d1qo00758k.

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For the first time, calcium hydride and palladium chloride were used to reduce a wide range of organic halides including aromatic bromides, aromatic chlorides, aromatic triflates, aliphatic bromides, aliphatic chlorides and trihalomethyl compounds.

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39

Brown, Allan F., Gad G. Yousef, Elizabeth H. Jeffery, et al. "Glucosinolate Profiles in Broccoli: Variation in Levels and Implications in Breeding for Cancer Chemoprotection." Journal of the American Society for Horticultural Science 127, no. 5 (2002): 807–13. http://dx.doi.org/10.21273/jashs.127.5.807.

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Ten broccoli [Brassica oleracea L. (Botrytis Group)] accessions were grown in several environments to estimate glucosinolate (GS) variability associated with genotype, environment, and genotype × environment interaction and to identify differences in the stability of GSs in broccoli florets. Significant differences in genetic variability were identified for aliphatic GSs but not for indolyl GSs. The percentage of GS variability attributable to genotype for individual aliphatic compounds ranged from 54.2% for glucoraphanin to 71.0% for progoitrin. For total indolyl GSs, the percentage of variab

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40

Šimon, T. "Aliphatic compounds, organic C and N and microbial biomass and its activity in long-term field experiment." Plant, Soil and Environment 51, No. 6 (2011): 276–82. http://dx.doi.org/10.17221/3586-pse.

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The content of aliphatic compounds, hydrophobicity index, organic C and N content and the microbial biomass and respiration activity were analysed in soil samples originating from different plots of a long-term field experiment (variants: nil, NPK &ndash; mineral fertilization: 64.6&ndash;100 kg/ha/year, FYM &ndash; farmyard manure and FYM + NPK) from three blocks (III, IV and B) with different crop rotation. Samples were taken from 0&ndash;200 mm layer in 2002 and 2003 (spring and autumn). The plots without any fertilization had the significantly lowest aliphatic compound cont

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41

Aranda, Carmen, Juan Carro, Alejandro González-Benjumea, et al. "Advances in enzymatic oxyfunctionalization of aliphatic compounds." Biotechnology Advances 51 (November 2021): 107703. http://dx.doi.org/10.1016/j.biotechadv.2021.107703.

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42

Helmchen, G., and A. Dahnz. "Enantioselective Allylic Substitutions with Aliphatic Nitro Compounds." Synfacts 2006, no. 5 (2006): 0469. http://dx.doi.org/10.1055/s-2006-934444.

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43

Bollinger, Jean-Claude, Raymond Houriet, and Theophile Yvernault. "Structure and Basicities of Aliphatic Organophosphorus Compounds." Phosphorus and Sulfur and the Related Elements 30, no. 3-4 (1987): 659. http://dx.doi.org/10.1080/03086648708079153.

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44

HARADA, Kazuho, Junichi YOKOYAMA, and Shonosuke ZEN. "Reactions of Aliphatic Nitro Compounds and Glycocyamidines." NIPPON KAGAKU KAISHI, no. 1 (1995): 47–56. http://dx.doi.org/10.1246/nikkashi.1995.47.

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45

Smith, B. V. "Chapter 5. Aliphatic compounds. Part (i) Hydrocarbons." Annual Reports Section "B" (Organic Chemistry) 82 (1985): 91. http://dx.doi.org/10.1039/oc9858200091.

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46

Smith, B. V. "Chapter 5. Aliphatic compounds. Part (i) Hydrocarbons." Annual Reports Section "B" (Organic Chemistry) 83 (1986): 77. http://dx.doi.org/10.1039/oc9868300077.

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47

Smith, B. V. "Chapter 5. Aliphatic compounds. Part (i) Hydrocarbons." Annual Reports Section "B" (Organic Chemistry) 84 (1987): 93. http://dx.doi.org/10.1039/oc9878400093.

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48

Thomas, S. E. "Chapter 5. Aliphatic compounds. Part (i) Hydrocarbons." Annual Reports Section "B" (Organic Chemistry) 85 (1988): 85. http://dx.doi.org/10.1039/oc9888500085.

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49

Hill, L., and S. E. Thomas. "Chapter 5. Aliphatic compounds. Part (i) Hydrocarbons." Annual Reports Section "B" (Organic Chemistry) 86 (1989): 87. http://dx.doi.org/10.1039/oc9898600087.

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50

Harrison, M. J., and S. E. Thomas. "Chapter 5. Aliphatic compounds. Part (i) Hydrocarbons." Annual Reports Section "B" (Organic Chemistry) 87 (1990): 101. http://dx.doi.org/10.1039/oc9908700101.

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