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Journal articles on the topic 'Tertiary acetylenic alcohol'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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1

Juraboev, Fozil Mamasolievich. "SYNTHESIS OF ACETYLENIC DIOLS BASED ON ACETYLENIC ALCOHOLS." Research Focus 1, no. 2 (2022): 17–22. https://doi.org/10.5281/zenodo.7237916.

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<em>This article examines the influence of various factors on the performance of the main product in the synthesis of acetylene diols based on direct condensation of acetylene alcohols with aldehydes and ketones.The influence of factors such as the structure and nature of acetylene alcohols on the yield of acetylenediols, the composition and nature of carbonyl compounds, temperature, catalyst, reaction duration has been studied.</em>
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2

Toda, Fumio, Koichi Tanaka, Hideo Ueda, and Tokio Ōshima. "Complex of Tertiary Acetylenic Alcohol and Brucine or Sparteine. X-Ray Crystal Structural Study and Application to Optical Resolution." Israel Journal of Chemistry 25, no. 3-4 (1985): 338–45. http://dx.doi.org/10.1002/ijch.198500055.

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3

Petukhov, V. N., S. A. Shchelkunov, O. A. Malyshev, D. A. Kubak, and S. V. Yudina. "Influence of Tertiary Acetylenic Alcohols on Coal Flotation." Coke and Chemistry 63, no. 11 (2020): 533–42. http://dx.doi.org/10.3103/s1068364x20110058.

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4

Gilazhov, Y. G., D. K. Kulbatyrov, M. D. Urazgalieva, N. K. Kuznetsova, and A. Zh Zhexembayeva. "Effectiveness of dimethylethynylcarbinol and methyl tert-butyl ether on octane number increase of gasoline compositions." Neft i Gaz 143, no. 5 (2024): 237–48. https://doi.org/10.37878/2708-0080/2024-5.18.

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Despite the significant increase in requirements to the quality of motor fuel, harmful exhaust gases from gasoline combustion are still a major environmental problem. Today gasoline occupies one of the leading positions among primary energy sources. The problem of improving the quality of gasoline is one of the urgent problems of the chemical industry. In order to reduce harmful exhaust emissions from internal combustion engines, improve the detonation resistance of fuels and utilize renewable fuels, many different oxygen-containing additives are added to base gasoline. The research and develo
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5

Punia, Lavisha, Karu Ramesh, and Gedu Satyanarayana. "Palladium mediated domino reaction: synthesis of isochromenes under aqueous medium." RSC Advances 10, no. 1 (2020): 338–49. http://dx.doi.org/10.1039/c9ra08792c.

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6

Toda, Fumio, and Koichi Tanaka. "Optical Resolution of Tertiary Acetylenic Alcohols and Secondary Alcohols by Complexation with Achiral Amines." Chemistry Letters 15, no. 11 (1986): 1905–8. http://dx.doi.org/10.1246/cl.1986.1905.

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7

Dikusar, E. A., N. G. Kozlov, V. M. Zelenkovskii, et al. "Peroxy-containing Tertiary Acetylenic Alcohols Derived from Cycloheptanone, Cyclododecanone, and (-)-R-Carvone." Russian Journal of General Chemistry 73, no. 8 (2003): 1277–81. http://dx.doi.org/10.1023/b:rugc.0000007657.56215.a3.

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8

SAKHAROV, B. N., M. A. LIPKIN, and V. S. MARKEVICH. "ChemInform Abstract: Meyer-Schuster Reaction of Tertiary Acetylenic Alcohols Bearing Cyclopropyl Substituents." ChemInform 24, no. 10 (2010): no. http://dx.doi.org/10.1002/chin.199310096.

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9

Dikusar, E. A. "Tertiary Acetylenic Alcohols and Peroxides Derived from 4,4'-Bis(dimethylamino)benzophenone (Michler's Ketone)." Russian Journal of General Chemistry 73, no. 9 (2003): 1406–9. http://dx.doi.org/10.1023/b:rugc.0000015988.84852.9d.

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10

Trofimov, Boris A., Elena Yu Schmidt, Elena V. Skital’tseva, Ivan A. Bidusenko, Nadezhda V. Zorina, and Al’bina I. Mikhaleva. "Base-catalyzed O-vinylation of tertiary propargylic alcohols with acetylene: First examples." Mendeleev Communications 22, no. 2 (2012): 62–63. http://dx.doi.org/10.1016/j.mencom.2012.03.002.

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11

Kozinskaya, Lyubov Konstantinovna, and Aziz Berdiyarovich Tadjiev. "SYNTHESIS OF TERTIARY ACETYLENIC ALCOHOLS DIBENZO-18-CROWN-6 FROM 4´, 4´´-DIAMINODIBENZO-18-CROWN-6." Austrian Journal of Technical and Natural Sciences, no. 9-10 (2021): 35–39. http://dx.doi.org/10.29013/ajt-21-9.10-35-39.

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12

Kozlov, N. G., E. A. Dikusar, V. M. Zelenkovskii, et al. "Tertiary Acetylenic Alcohols, Ethers, and Esters on the Basis of Isocamphanone, Camphor, Fenchone, Isofenchone, and Adamanthanone." Russian Journal of General Chemistry 74, no. 6 (2004): 890–96. http://dx.doi.org/10.1023/b:rugc.0000042425.08789.c4.

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13

Rodríguez, Ricardo I., Elsie Ramírez, Francisco Yuste, Rubén Sánchez-Obregón, and José Alemán. "Asymmetric Synthesis of Secondary and Tertiary Propargylic Alcohols by Umpolung of Acetylenic Sulfones and ortho-Sulfinyl Carbanions." Journal of Organic Chemistry 83, no. 4 (2018): 1940–47. http://dx.doi.org/10.1021/acs.joc.7b02887.

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14

Trofimov, Boris A., Elena Yu Schmidt, Elena V. Skital'tseva, Ivan A. Bidusenko, Nadezhda V. Zorina, and Al'bina I. Mikhaleva. "ChemInform Abstract: Base-Catalyzed O-Vinylation of Tertiary Propargylic Alcohols with Acetylene: First Examples." ChemInform 43, no. 34 (2012): no. http://dx.doi.org/10.1002/chin.201234037.

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15

Tolkacheva, L. N., V. P. Kislyi, S. Z. Taits, and V. V. Semenov. "ChemInform Abstract: Hydrogenation on Granular Palladium-Containing Catalysts. Part 1. Hydrogenation of Tertiary Acetylene Alcohols." ChemInform 33, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.200241061.

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16

Johnson, Erika L., Christy A. Smith, Kirk T. O'Reilly, and Michael R. Hyman. "Induction of Methyl Tertiary Butyl Ether (MTBE)-Oxidizing Activity in Mycobacterium vaccae JOB5 by MTBE." Applied and Environmental Microbiology 70, no. 2 (2004): 1023–30. http://dx.doi.org/10.1128/aem.70.2.1023-1030.2004.

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ABSTRACT Alkane-grown cells of Mycobacterium vaccae JOB5 cometabolically degrade the gasoline oxygenate methyl tertiary butyl ether (MTBE) through the activities of an alkane-inducible monooxygenase and other enzymes in the alkane oxidation pathway. In this study we examined the effects of MTBE on the MTBE-oxidizing activity of M. vaccae JOB5 grown on diverse nonalkane substrates. Carbon-limited cultures were grown on glycerol, lactate, several sugars, and tricarboxylic acid cycle intermediates, both in the presence and absence of MTBE. In all MTBE-containing cultures, MTBE consumption occurre
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17

Shmidt, E. Yu, I. A. Bidusenko, N. I. Protsuk, A. I. Mikhaleva, and B. A. Trofimov. "Improved synthesis of tertiary propargyl alcohols by the Favorskii reaction of alkyl aryl (hetaryl) ketones with acetylene." Russian Journal of Organic Chemistry 49, no. 1 (2013): 8–11. http://dx.doi.org/10.1134/s1070428013010028.

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18

Shmidt, E. Yu, I. A. Bidusenko, N. I. Protsuk, A. I. Mikhaleva, and B. A. Trofimov. "ChemInform Abstract: Improved Synthesis of Tertiary Propargyl Alcohols by the Favorskii Reaction of Alkyl Aryl (Hetaryl) Ketones with Acetylene." ChemInform 44, no. 25 (2013): no. http://dx.doi.org/10.1002/chin.201325053.

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19

Gilazhov, Y. G., D. K. Kulbatyrov, M. D. Urazgalieva, and K. R. Maksot. "Efficiency of oxygenates on increase of octane number of reforming gasoline." Neft i Gaz, no. 3 (June 30, 2024): 136–47. http://dx.doi.org/10.37878/2708-0080/2024-3.11.

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At present, gasoline occupies one of the leading places among primary energy sources. The need of mankind in it, in its high quality, is greater than in any other fraction of hydrocarbons. Therefore, very high requirements are made to the operational properties of automobile gasoline, and the problem of improving the quality of gasoline is one of the urgent problems of the chemical industry. Modern vehicles require fuel with a high-octane number with properties preventing detonation and having octane numbers of 92, 95 and 98 for engines. High anti-detonation performance can be achieved through
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20

Savarimuthu, Sebastian Antony, Hajeeth Thankappan, Selvaraj Augustine Thomas, and Devarajan Gnanaprakasi Leo Prakash. "Sodium Tertiary Pentoxide: A Mild and Efficient Base to Make C-C Bond between Acetylenes and Aldehydes (or) Ketones Producing Propargyl Alcohols." ChemistrySelect 3, no. 29 (2018): 8479–82. http://dx.doi.org/10.1002/slct.201801640.

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21

Dikusar, E. A., N. G. Kozlov, K. L. Moiseichuk, and V. I. Potkin. "Tertiary Acetylene Alcohols Prepared from 1-Octadecyne." ChemInform 34, no. 14 (2003). http://dx.doi.org/10.1002/chin.200314180.

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22

TODA, F., and K. TANAKA. "ChemInform Abstract: Optical Resolution of Tertiary Acetylenic Alcohols and Secondary Alcohols by Complexation with Achiral Amines." ChemInform 18, no. 23 (1987). http://dx.doi.org/10.1002/chin.198723069.

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23

TROFIMOV, B. A., L. N. SOBENINA, S. E. KOROSTOVA, et al. "ChemInform Abstract: Synthesis of Tertiary Acetylenic Alcohols and Their Ethers in the System KOH-DMSO." ChemInform 18, no. 44 (1987). http://dx.doi.org/10.1002/chin.198744121.

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24

Yushina, T. I., B. Purev, and B. Namuungerel. "Substantiation of the Erdenetiyn-Ovoo copper-molybdenum ore flotation technology with the use of tertiary acetylene alcohol." Non-ferrous Metals, December 29, 2020, 3–10. http://dx.doi.org/10.17580/nfm.2020.02.01.

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The article presents the results of a study of the factors affecting the efficiency of the copper-molybdenum ore flotation. The objective of this work was to substantiate and develop a reagent mode for flotation of the Erdenetiyn-Ovoo porphyry copper ores, which makes possible extracting main copper and molybdenum minerals into corresponding concentrates more fully and selectively. It is shown that the use of a DC-80 (2-methyl-3-butin-2-ol) flotation reagent in assosiation with the main base mode reagents — an AERO MX-5152 (a mixture of allyl ethers of xanthogenic acids with n-butyloxycarbonyl
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25

Potkin, V. I., E. A. Dikusar, and N. G. Kozlov. "Tertiary Acetylenic Alcohols and Diols on the Basis of Phenylacetylene and 2-Methyl-3-butyn-2-ol." ChemInform 34, no. 16 (2003). http://dx.doi.org/10.1002/chin.200316067.

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