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Статті в журналах з теми "Decalones"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Decalones.

Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 29 січня 2023

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1

Huffman, John W., and William H. Balke. "Enolization of 2-decalones." Journal of Organic Chemistry 53, no. 16 (August 1988): 3828–31. http://dx.doi.org/10.1021/jo00251a030.

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2

J. Hart, David, and Shung C. Wu. "Gelsemine Model Studies: Alkoxymethylations of Decalones and Indoles." HETEROCYCLES 35, no. 1 (1993): 135. http://dx.doi.org/10.3987/com-92-s57.

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3

Suh, Young-Ger, Hwa-Soon Kim, P. Raja kumar, Nam-Song Choi, and Jae-Kyung Jung. "Practical and versatile syntheses of angular hydroxymethylated decalones." Tetrahedron 54, no. 50 (December 1998): 15161–66. http://dx.doi.org/10.1016/s0040-4020(98)00965-x.

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4

Ferraz, Helena M. C., and Luiz F. Silva Jr. "Thallium trinitrate mediated ring contraction of cis-2-decalones." Journal of the Brazilian Chemical Society 12, no. 4 (August 2001): 548–51. http://dx.doi.org/10.1590/s0103-50532001000400018.

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5

Solladié-Cavallo, Arlette, Loïc Jierry, Arlette Klein, Michel Schmitt та Richard Welter. "α-Fluoro decalones as chiral epoxidation catalysts: fluorine effect". Tetrahedron: Asymmetry 15, № 24 (грудень 2004): 3891–98. http://dx.doi.org/10.1016/j.tetasy.2004.10.033.

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6

Piriou, Francois, and Hugues d'Orchymont. "Synthesis and Conformational Analysis of 3-Amino-2-decalones." Magnetic Resonance in Chemistry 34, no. 3 (March 1996): 213–20. http://dx.doi.org/10.1002/(sici)1097-458x(199603)34:3<213::aid-omr868>3.0.co;2-a.

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7

Suh, Young-Ger, Hwa-Soon Kim, P. Raja Kumar, Nam-Song Choi, and Jae-Kyung Jung. "ChemInform Abstract: Practical and Versatile Syntheses of Angular Hydroxymethylated Decalones." ChemInform 30, no. 17 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199917108.

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8

HART, D. J., and S. C. WU. "ChemInform Abstract: Gelsemine Model Studies: Alkoxymethylations of Decalones and Indoles." ChemInform 24, no. 29 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199329175.

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9

Ziegler, Frederick E., Ki Jun Hwang, John F. Kadow, Scott I. Klein, Uttam K. Pati, and Tein Fu Wang. "Practical routes to two functionalized decalones for the synthesis of quassinoids." Journal of Organic Chemistry 51, no. 24 (November 1986): 4573–79. http://dx.doi.org/10.1021/jo00374a016.

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10

An, Yi Zhong, and David F. Wiemer. "Regiochemistry of vinyl phosphate/.beta.-keto phosphonate rearrangements in functionalized cyclohexanones and decalones." Journal of Organic Chemistry 57, no. 1 (January 1992): 317–21. http://dx.doi.org/10.1021/jo00027a055.

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11

Sutton, G. Paul, and Peter C. Jurs. "Simulation of carbon-13 nuclear magnetic resonance spectra of alkyl-substituted cyclohexanones and decalones." Analytical Chemistry 61, no. 8 (April 15, 1989): 863–71. http://dx.doi.org/10.1021/ac00183a017.

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12

Ferraz, Helena M. C., and Luiz F. Silva. "Thallium Trinitrate Mediated Ring Contraction oftrans-2-Decalones: An Alternative Entry to the Hydrindane System." Journal of Organic Chemistry 63, no. 5 (March 1998): 1716–18. http://dx.doi.org/10.1021/jo971585r.

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13

Wasnaire, Pierre, Marianne Wiaux, Roland Touillaux, and István E. Markó. "Reductive cyclisation of Morita–Baylis–Hillman adducts. A simple approach towards substituted hydrindanones and decalones." Tetrahedron Letters 47, no. 6 (February 2006): 985–89. http://dx.doi.org/10.1016/j.tetlet.2005.11.143.

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14

Jansen, Ben J. M., Cindy C. J. Hendrikx, Nikolai Masalov, Gerrit A. Stork, Tommi M. Meulemans, Fliur Z. Macaev, and Aede de Groot. "Enantioselective Synthesis of Functionalised Decalones by Robinson Annulation of Substituted Cyclohexanones, Derived from R-(−)-Carvone." Tetrahedron 56, no. 14 (March 2000): 2075–94. http://dx.doi.org/10.1016/s0040-4020(00)00110-1.

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15

Swarts, Henk J., Anja A. Haaksman, Ben J. M. Jansen, and Aede de Groot. "The synthesis of chiral decalones, (−)-1,1,4a-trimethyl-2-decalol and (+)-geosmin from S-(+)-carvone (part 3)." Tetrahedron 48, no. 26 (January 1992): 5497–508. http://dx.doi.org/10.1016/s0040-4020(01)88303-4.

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16

Liu, Hsing-Jang, and Eric N. C. Browne. "Diels–Alder reactions of 4,4-dimethyl-2-cyclohexenones. A direct route to the 4,4-dimethyl-1-decalones." Canadian Journal of Chemistry 65, no. 6 (June 1, 1987): 1262–78. http://dx.doi.org/10.1139/v87-214.

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Анотація:

Diels–Alder additions to enones 1 and 2, synthetic equivalents of the synthon 3, were studied using a variety of hydrocarbon dienes. The two enones have been shown to be effective and synthetically useful dienophiles. Spectroscopic (especially 1H and 13C magnetic resonance) and chemical techniques were used to define unambiguously the full structures of the adducts. The structures of the various reaction products were used to draw qualitative conclusions about the nature of the transition states involved and the various electronic and steric effects that play a role in the mechanistic course of the Diels–Alder reaction.

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17

Richter, Friedrich, and Hans-Hartwig Otto. "Synthesis of nitro-substituted decalones by double Michael reaction, sequential Michael reaction, and by Diels-Alder reaction." Tetrahedron Letters 28, no. 26 (1987): 2945–46. http://dx.doi.org/10.1016/s0040-4039(00)96250-6.

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18

Jansen, Ben J. M., Cindy C. J. Hendrikx, Nikolai Masalov, Gerrit A. Stork, Tommi M. Meulemans, Fliur Z. Macaev, and Aede de Groot. "ChemInform Abstract: Enantioselective Synthesis of Functionalized Decalones by Robinson Annulation of Substituted Cyclohexanones, Derived from R-(-)-Carvone." ChemInform 31, no. 28 (June 7, 2010): no. http://dx.doi.org/10.1002/chin.200028101.

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19

Holton, Robert A., and Robert M. Kennedy. "Stereocontrol of the metal-ammonia reduction: formation of either cis- or trans-fused decalones from a common intermediate." Tetrahedron Letters 28, no. 3 (January 1987): 303–6. http://dx.doi.org/10.1016/s0040-4039(00)95713-7.

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20

Richter, Friedrich, and Hans-Hartwig Otto. "Synthesis of substituted decalones by diels-alder reaction or by sequential michael reaction - which one is more selective?" Tetrahedron Letters 26, no. 36 (January 1985): 4351–54. http://dx.doi.org/10.1016/s0040-4039(00)98732-x.

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21

Seth, Punit P., Deqi Chen, Junquan Wang, Xiuchun Gao, and Nancy I. Totah. "The Dihydropyrone Diels–Alder Reaction: Development and Application to the Synthesis of Highly Functionalized 1-Oxa-4-decalones." Tetrahedron 56, no. 52 (December 2000): 10185–95. http://dx.doi.org/10.1016/s0040-4020(00)00863-2.

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22

SWARTS, H. J., A. A. HAAKSMA, B. J. M. JANSEN, and A. DE GROOT. "ChemInform Abstract: The Synthesis of Chiral Decalones, (-)-1,1,4a-Trimethyl-2-decalol and ( +)-Geosmin from S-(+)-Carvone. Part 3." ChemInform 23, no. 42 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199242232.

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23

FERRAZ, H. M. C., and L. F. JUN SILVA. "ChemInform Abstract: Thallium Trinitrate Mediated Ring Contraction of trans-2-Decalones: An Alternative Entry to the Hydrindan System." ChemInform 29, no. 30 (June 20, 2010): no. http://dx.doi.org/10.1002/chin.199830113.

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24

Hagiwara, Hisahiro, Tsutomu Akama, Akihiro Okano, and Hisashi Uda. "Asymmetric Two-Fold Michael Reaction. Synthesis of Optically Active 4-Substituted 1-Decalones from Trimethylsilyl Enol Ether of 1-Acetylcyclohexene." Chemistry Letters 18, no. 12 (December 1989): 2149–52. http://dx.doi.org/10.1246/cl.1989.2149.

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25

Seth, Punit P., Deqi Chen, Junquan Wang, Xiuchun Gao, and Nancy I. Totah. "ChemInform Abstract: The Dihydropyrone Diels-Alder Reaction: Development and Application to the Synthesis of Highly Functionalized 1-Oxa-4-decalones." ChemInform 32, no. 16 (April 17, 2001): no. http://dx.doi.org/10.1002/chin.200116143.

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26

Hagiwara, Hisahiro, Tsutomu Akama, Akihiro Okano, and Hisashi Uda. "Annulation by sequential double Michael reaction; synthesis of decalones and its application to the syntheses of Îµ-cadinene, khusitone and khusilal." J. Chem. Soc., Perkin Trans. 1, no. 18 (1993): 2173–84. http://dx.doi.org/10.1039/p19930002173.

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27

Verstegen-Haaksma, Anja A., Henk J. Swarts, Ben J. M. Jansen, and Aede de Groot. "S-(+)-carvone as starting material in synthesis (part 4). Conjugate addition of cyanide and Grignard nucleophiles followed by annulation to functionalized decalones." Tetrahedron 50, no. 33 (January 1994): 10073–82. http://dx.doi.org/10.1016/s0040-4020(01)89623-x.

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28

HAGIWARA, H., T. AKAMA, A. OKANO, and H. UDA. "ChemInform Abstract: Annulation by Sequential Double Michael Reaction; Synthesis of Decalones and Its Application to the Syntheses of .epsilon.-Cadinene, Khusitone and Khusilal." ChemInform 25, no. 1 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199401171.

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29

Hagiwara, Hisahiro, Tsutomu Akama, Akihiro Okano та Hisashi Uda. "Synthesis of Substituted 2-Decalones from 1-Acetylcyclohexenes and α-Trimethylsilyl α,β-Unsaturated Carbonyl Compounds by Two-Fold Michael Reactions. Synthesis of (±)-Khusitone". Chemistry Letters 17, № 10 (5 жовтня 1988): 1793–96. http://dx.doi.org/10.1246/cl.1988.1793.

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30

VERSTEGEN-HAAKSMA, A. A., H. J. SWARTS, B. J. M. JANSEN, and A. DE GROOT. "ChemInform Abstract: S-(+)-Carvone as Starting Material in Synthesis. Part 4. Conjugate Addition of Cyanide and Grignard Nucleophiles Followed by Annulation to Functionalized Decalones." ChemInform 26, no. 3 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199503212.

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31

Hagiwara, Hisahiro, Akihiro Okano, Tsutomu Akama та Hisashi Uda. "Lewis acid assisted annelation of trimethylsilyl enol ethers of 1-acetylcyclohexenes with α,β-unsaturated carbonyl compounds to give substituted 2-decalones; synthesis of (±)-Îµ-cadinene". J. Chem. Soc., Chem. Commun., № 18 (1987): 1333–35. http://dx.doi.org/10.1039/c39870001333.

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32

BLAY, G., R. SCHRIJVERS, J. B. P. A. WIJNBERG та A. DE GROOT. "ChemInform Abstract: Regioselective Intramolecular Base-Induced Synthesis of α,β- Unsaturated Acyldecalins from Decalones via Carbon Homologation with TosMIC. Synthesis of (.+-.)-6-Eudesmen-4α-ol and (.+-.)- Vetiselinene." ChemInform 26, № 34 (17 серпня 2010): no. http://dx.doi.org/10.1002/chin.199534214.

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33

Blay, Gonzalo, Robert Schrijvers, Joannes B. P. A. Wijnberg, and Aede de Groot. "Regioselective intramolecular base-Induced synthesis of .alpha.,.beta.-Unsaturated. Acyldecalins from Decalones via Carbon Homologation with isocyanomethyl Tosylate (TosMIC). Synthesis of (.+-.)-6-Eudesmen-4.alpha.-ol and (.+-.)-Vetiselinene." Journal of Organic Chemistry 60, no. 7 (April 1995): 2188–94. http://dx.doi.org/10.1021/jo00112a044.

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34

Wu, Yun Dong, John A. Tucker, and K. N. Houk. "Stereoselectivities of nucleophilic additions to cyclohexanones substituted by polar groups. Experimental investigation of reductions of trans-decalones and theoretical studies of cyclohexanone reductions. The influence of remote electrostatic effects." Journal of the American Chemical Society 113, no. 13 (June 1991): 5018–27. http://dx.doi.org/10.1021/ja00013a042.

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35

Lévy, Jean, Jean-Yves Laronze, and Janos-Sapi. "The Hofmann-like fragmentation induced by n-acylation of 1-methyl-1-AZA-4-cyclanones and its use in the synthesis of 2-AZA-hydrindanones and 2-AZA-decalones." Tetrahedron Letters 29, no. 27 (January 1988): 3303–6. http://dx.doi.org/10.1016/0040-4039(88)85147-5.

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36

Carman, RM, AC Garner, and WT Robinson. "The Structure of the Decalone Obtained From the Oxidation of Guaiol." Australian Journal of Chemistry 45, no. 2 (1992): 327. http://dx.doi.org/10.1071/ch9920327.

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Анотація:

The structure of the decalone previously reported from the oxidation of guaiol has, after X-ray crystallographic analysis, been revised to structure (3c) which contains a cis -fused ring system. Deuteration studies give insight into the conformation of the transition state during the reaction.

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37

Aubé, Jeffrey, and Marlys Hammond. "Directed regiochemicalcontrolin thering expansion reactionsofasubstituted trans-decalone." Tetrahedron Letters 33, no. 10 (March 1992): 1246. http://dx.doi.org/10.1016/s0040-4039(00)91593-4.

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38

Gramain, J. C., та J. C. Quirion. "Carbon-13 NMR studies in the polycyclic hydrocarbon series. A new method for the identification of carbons α to a carbonyl group. Complete assignment of the13C NMR spectra of severalcis-decalins,cis-decalones,cis-hydrindanones and 13α,14α- and 13β,14β-steroids". Magnetic Resonance in Chemistry 24, № 11 (листопад 1986): 938–46. http://dx.doi.org/10.1002/mrc.1260241103.

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39

Fossey, Jacques, Daniel Lefort, Massoud Massoudi, Jean-Yves Nedelec, and Jeanine Sorba. "Régiosélectivité et stéréosélectivité de l'hydroxylation homolytique des hydrocarbures par le peracide benzoïque." Canadian Journal of Chemistry 63, no. 3 (March 1, 1985): 678–80. http://dx.doi.org/10.1139/v85-111.

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Анотація:

Cyclohexane, methylcyclohexane, and adamantane are hydroxylated by a radical process using perbenzoic acid. A regioselectivity of 60–90% in favour of tertiary alcohols is noted. In the case of cis and trans decalins, stereoselection leading to 9-decalols can reach 97%. Such a stereoselectivity for hydroxylation by use of a peracid does not necessarily indicate lack of a radical pathway.

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40

Abboud, K. A., Y. Xie, and E. J. Enholm. "A cis-Fused Decalone and a Bicyclo[4.3.1]decanone Ring System." Acta Crystallographica Section C Crystal Structure Communications 52, no. 7 (July 15, 1996): 1829–31. http://dx.doi.org/10.1107/s0108270196000121.

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41

Gardner, Jared. "Covered Wagons and Decalogues: Paramount's Myths of Origins." Yale Journal of Criticism 13, no. 2 (2000): 361–89. http://dx.doi.org/10.1353/yale.2000.0019.

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42

Zewge, D., A. P. J. Brunskill, R. A. Lalancette, and H. W. Thompson. "(±)-cis-10-Carboxymethyl-2-decalone: Catemeric Hydrogen Bonding in an ∊-Keto Acid." Acta Crystallographica Section C Crystal Structure Communications 54, no. 11 (November 15, 1998): 1651–53. http://dx.doi.org/10.1107/s0108270198007495.

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43

Morejon-Llamas, Noemi. "Desinformación y alfabetización mediática desde las instituciones: los decálogos contra las fake news." Las Relaciones Públicas en el nuevo milenio: retos y oportunidades 10, no. 20 (December 22, 2020): 111–34. http://dx.doi.org/10.5783/rirp-20-2020-07-111-134.

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Анотація:

In an environment characterized by infoxication, the speed and immediacy of information circulation, the emotionality of the messages, the virality, the horizontality in the content production, and the lack of trust in institutions and media, we consider vital the role that institutions play through their institutional advertising to deal with misinformation. For this reason, our research aims to establish whether there is coherence between the institutional visual campaigns, about fake news during Covid-19 and the recommendations of national and international bodies, such as the European Commission, UNESCO and the WHO. Based on the importance that these organizations give to the contextualization and consequences of the problem, we analyzed a representative sample of 20 visual resources through content analysis and discursive analysis to assess whether the approach of these campaigns is appropiate. We also studied the virality of the information through an analysis of the content diffusion on Twitter. Our results indicated an insufficient number of posters and decalogues, along with their limitation in dealing with disinformation. First of all, we observed a lack of coordination in the framing of the problem, because despite the detection mechanisms (contrast, source analysis, medium) are specified, and the non-viralization / dissemination is urged, intentionality and repercussion are directly and indirectly ignored. A 60% of the analysed decalogues did not mention the consequences of disinformation, neither in the short nor in the long term. A 20% explains the economic or political benefit that could be obtained from the dissemination of a deception and 15% explains the possible damage to health or reputation. Only a 5% mention the polarisation of public opinion. The secondary effects of fake news that institutional advertising exposed were: the damage to the digital identity, discrimination against individuals, the advantage of unethical businesses, the reduction in media confidence, the decrease in critical thinking, and the undermining of the confidence of institutions that do not even appear in the decalogues. Secondly, we appreciated a restriction of the campaigns to the child and adolescent public, as well as to adults in the role of parents. Dissemination is also a pending task for the institutions, since none of the initiatives were successful and went viral on Twitter, even less so in the case of the campaigns that we consider more complete in their approach. The conclusions of this work invite to revisit the institutional communication and advertising as tools for media and digital literacy through coordination with the media, journalists, educators, politicians and experts in the field. Order PCM / 1030/2020, of October 30, which publishes the procedure for action against disinformation opens a new path to study information disorders in Spain. From this point, the objective should be to analyse it from a structural prism which empowers citizens, not to assign them total responsibility for how they receive information.

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44

Nozawa, Koohei, Shoichi Nakajima, Shun-ichi Udagawa, and Ken-ichi Kawai. "Isolation and structure of a new 1-decalone derivative, rapiculine, from Ramichloridium apiculatum." Journal of the Chemical Society, Perkin Transactions 1, no. 3 (1991): 537. http://dx.doi.org/10.1039/p19910000537.

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45

Aubé, Jeffrey, and Marlys Hammond. "Directed regiochemical control in the ring expansion reactions of a substituted trans-decalone." Tetrahedron Letters 31, no. 21 (1990): 2963–66. http://dx.doi.org/10.1016/s0040-4039(00)88999-6.

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46

Gao, Jianxin, Christopher K. Njue, Jeremiah K. N. Mbindyo, and James F. Rusling. "Mechanism of stereoselective production of trans-1-decalone by electrochemical catalysis in microemulsions." Journal of Electroanalytical Chemistry 464, no. 1 (March 1999): 31–38. http://dx.doi.org/10.1016/s0022-0728(98)00463-x.

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47

Rontani, J.-F., C. Aubert, and G. Giusti. "A new fragmentation pathway of cis-1-decalone involving a double McLafferty rearrangement." Organic Mass Spectrometry 24, no. 10 (October 1989): 967–68. http://dx.doi.org/10.1002/oms.1210241023.

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48

CARMAN, R. M., A. C. GARNER, and W. T. ROBINSON. "ChemInform Abstract: The Structure of the Decalone Obtained from the Oxidation of Guaiol." ChemInform 23, no. 21 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199221251.

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49

ABBOUD, K. A., Y. XIE, and E. J. ENHOLM. "ChemInform Abstract: A cis-Fused Decalone and a Bicyclo(4.3.1)decanone Ring System." ChemInform 27, no. 45 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199645044.

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50

Utomi, Patrick. "Legitimacy and Governance: One More Year of Military Rule in Nigeria." Issue 14 (1985): 39–42. http://dx.doi.org/10.1017/s0047160700505939.

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When the phenomenon of military rule in Africa first attracted the attention of researchers, the thrust of inquiry was the explanation of the apparent anomaly of the coup d’etat. After years of effort, epitomized by Samuel Decalo’s work on Coups and Army Rule in Africa, a consensus seemed to have emerged that a general theory explaining military intervention could not be found. Scholarship thus turned its focus to the military as policymakers. This essay shall seek to do both — explain military intervention; and evaluate the performance of the military as policymakers. Nigeria, which is into its second epoch of military rule, provides an appropriate case study.

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