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Artigos de revistas sobre o tema "Thionolactones"

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Autor: Grafiati

Publicado: 25 de maio de 2024

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1

Chayajarus, Kampanart, e Antony J. Fairbanks. "Efficient synthesis of carbohydrate thionolactones". Tetrahedron Letters 47, n.º 21 (maio de 2006): 3517–20. http://dx.doi.org/10.1016/j.tetlet.2006.03.104.

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2

Iwasa, Seiji, Makoto Yamamoto, Shigeo Kohmoto e Kazutoshi Yamada. "Synthesis of thionolactones from homoallylic xanthates". Journal of the Chemical Society, Perkin Transactions 1, n.º 5 (1991): 1173. http://dx.doi.org/10.1039/p19910001173.

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3

Wang, Wendong, Pornpun Rattananakin e Peter G. Goekjian. "Synthesis of N‐Glycoside Analogs via Thionolactones". Journal of Carbohydrate Chemistry 22, n.º 7-8 (31 de dezembro de 2003): 743–51. http://dx.doi.org/10.1081/car-120026472.

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4

IWASA, S., M. YAMAMOTO, S. KOHMOTO e K. YAMADA. "ChemInform Abstract: Synthesis of Thionolactones from Homoallylic Xanthates." ChemInform 22, n.º 33 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199133165.

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5

Wilkinson, Brendan L., e Antony J. Fairbanks. "One-pot synthesis of carbohydrate thionolactones from 1-thiosugars". Tetrahedron Letters 49, n.º 33 (agosto de 2008): 4941–43. http://dx.doi.org/10.1016/j.tetlet.2008.05.145.

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6

Bringmann, Gerhard, Andreas Wuzik, Jörg Kümmel e Wolfdieter A. Schenk. "Atropo-Enantioselective Ring Cleavage of Lewis Acid Modified Biaryl Thionolactones†,‡". Organometallics 20, n.º 8 (abril de 2001): 1692–94. http://dx.doi.org/10.1021/om001040e.

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7

Milewska, Maria J., Maria Gdaniec e Tadeusz Poloński. "Synthesis, stereochemistry, and chiroptical spectra of cyclopropyl lactones and thionolactones". Tetrahedron: Asymmetry 7, n.º 11 (novembro de 1996): 3169–80. http://dx.doi.org/10.1016/0957-4166(96)00419-3.

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8

Lee, Hyeon Kyu, Jia Kim e Chwang Siek Pak. "Reaction of thionolactones with zinc enolate: new synthesis of vinylogous carbonates". Tetrahedron Letters 40, n.º 34 (agosto de 1999): 6267–70. http://dx.doi.org/10.1016/s0040-4039(99)01231-9.

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9

Filippi, Jean-Jacques, Xavier Fernandez e Elisabet Duñach. "Lewis acid-catalysed isomerisation of thionolactones to thiolactones: inversion of configuration". Tetrahedron Letters 47, n.º 34 (agosto de 2006): 6067–70. http://dx.doi.org/10.1016/j.tetlet.2006.06.104.

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10

Beck, Thomas, e Armin Mosandl. "γ(δ)-Thionolactones - Enantioselective Capillary GC and Sensory Characteristics of Enantiomers". Journal of High Resolution Chromatography 22, n.º 2 (1 de fevereiro de 1999): 89–92. http://dx.doi.org/10.1002/(sici)1521-4168(19990201)22:2<89::aid-jhrc89>3.0.co;2-e.

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11

Jang, Doo Ok, e Seong Ho Song. "ChemInform Abstract: Organotin Hydride Catalyzed Radical Desulfurization of Thionoesters and Thionolactones." ChemInform 31, n.º 40 (3 de outubro de 2000): no. http://dx.doi.org/10.1002/chin.200040050.

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12

Nicolaou, K. C., D. G. McGarry, P. K. Somers, B. H. Kim, W. W. Ogilvie, G. Yiannikouros, C. V. C. Prasad, C. A. Veale e R. R. Hark. "Synthesis of medium-sized ring ethers from thionolactones. Applications to polyether synthesis". Journal of the American Chemical Society 112, n.º 17 (agosto de 1990): 6263–76. http://dx.doi.org/10.1021/ja00173a013.

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13

Nicolaou, Kyriacos C., Mitsunobu Sato, Emmanuel A. Theodorakis e Neil D. Miller. "Conversion of thionoesters and thionolactones to ethers; a general and efficient radical desulfurisation". Journal of the Chemical Society, Chemical Communications, n.º 15 (1995): 1583. http://dx.doi.org/10.1039/c39950001583.

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14

Lee, Hyeon Kyu, Jia Kim e Chwang Siek Pak. "ChemInform Abstract: Reaction of Thionolactones with Zinc Enolate: New Synthesis of Vinylogous Carbonates." ChemInform 30, n.º 45 (12 de junho de 2010): no. http://dx.doi.org/10.1002/chin.199945081.

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15

Jang, Doo Ok, Seong Ho Song e Dae Hyan Cho. "Conversion of esters and lactones to ethers via thionoesters and thionolactones using reductive radical desulfurization". Tetrahedron 55, n.º 11 (março de 1999): 3479–88. http://dx.doi.org/10.1016/s0040-4020(98)01156-9.

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16

NICOLAOU, K. C., M. SATO, E. A. THEODORAKIS e N. D. MILLER. "ChemInform Abstract: Conversion of Thionoesters and Thionolactones to Ethers; a General and Efficient Radical Desulfurization." ChemInform 26, n.º 49 (17 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199549062.

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17

Huang, Ya-Qing, Xiong-Zhi Huang e Pei-Qiang Huang. "Synthesis of 5-(1-Alkoxyalkylidene)tetronates by Direct Condensation Reactions of Tetronates with Thionolactones and Thionoesters". Journal of Organic Chemistry 86, n.º 3 (25 de janeiro de 2021): 2359–68. http://dx.doi.org/10.1021/acs.joc.0c02502.

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18

Yuan, Pengjun, Yangyang Sun, Xiaowei Xu, Yi Luo e Miao Hong. "Towards high-performance sustainable polymers via isomerization-driven irreversible ring-opening polymerization of five-membered thionolactones". Nature Chemistry 14, n.º 3 (25 de novembro de 2021): 294–303. http://dx.doi.org/10.1038/s41557-021-00817-9.

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19

Nicolaou, K. C., D. G. McGarry, P. K. Somers, C. A. Veale e G. T. Furst. "Nucleophilic additions to thionolactones. New synthetic technology for the construction of medium and large ring ethers". Journal of the American Chemical Society 109, n.º 8 (abril de 1987): 2504–6. http://dx.doi.org/10.1021/ja00242a041.

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20

Schenk, W. A., T. Beucke, J. Kummel, F. Servatius, N. Sonnhalter, G. Bringmann e A. Wuzik. "ChemInform Abstract: Stereo- and Enantioselective Reactions of Thioaldehydes, Thioketones, Thioketenes, and Thionolactones Mediated by Ruthenium Complexes". ChemInform 33, n.º 15 (22 de maio de 2010): no. http://dx.doi.org/10.1002/chin.200215276.

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21

MILEWSKA, M. J., M. GDANIEC e T. POLONSKI. "ChemInform Abstract: Synthesis, Stereochemistry, and Chiroptical Spectra of Cyclopropyl Lactones (cf. (V)) and Thionolactones (cf. (VI))". ChemInform 28, n.º 12 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199712098.

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22

Zaorska, Ewelina, Marta Gawryś-Kopczyńska, Ryszard Ostaszewski, Marcin Ufnal e Dominik Koszelewski. "Evaluation of thionolactones as a new type of hydrogen sulfide (H2S) donors for a blood pressure regulation". Bioorganic Chemistry 108 (março de 2021): 104650. http://dx.doi.org/10.1016/j.bioorg.2021.104650.

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23

Bachi, Mario D., e Eric Bosch. "Free radical cyclization of thionocarbonic acid derivatives of 4-phenyl-3-butenol. A new route to thionolactones". Journal of Organic Chemistry 54, n.º 6 (março de 1989): 1234–36. http://dx.doi.org/10.1021/jo00267a002.

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24

Jang, Doo Ok, Seong Ho Song e Dae Hyan Cho. "ChemInform Abstract: Conversion of Esters and Lactones to Ethers via Thionoesters and Thionolactones Using Reductive Radical Desulfurization." ChemInform 30, n.º 30 (14 de junho de 2010): no. http://dx.doi.org/10.1002/chin.199930065.

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25

Bingham, Nathaniel M., e Peter J. Roth. "Degradable vinyl copolymers through thiocarbonyl addition–ring-opening (TARO) polymerization". Chemical Communications 55, n.º 1 (2019): 55–58. http://dx.doi.org/10.1039/c8cc08287a.

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26

Schenk, Wolfdieter A., Jörg Kümmel, Irene Reuther, Nicolai Burzlaff, Andreas Wuzik, Olaf Schupp e Gerhard Bringmann. "Enantioselective Organic Syntheses Using Chiral Transition Metal Complexes, 9 Atropo-Diastereoselective Ring Opening of Biaryl Thionolactones Using [CpRu{(S,S)-CHIRAPHOS}]+ as a Chiral Auxiliary". European Journal of Inorganic Chemistry 1999, n.º 10 (outubro de 1999): 1745–56. http://dx.doi.org/10.1002/(sici)1099-0682(199910)1999:10<1745::aid-ejic1745>3.0.co;2-1.

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27

Takano, Seiichi, Shun’ichi Tomita, Michiyasu Takahashi e Kunio Ogasawara. "Thionolactone Claisen Rearrangement". Chemistry Letters 16, n.º 7 (5 de julho de 1987): 1379–80. http://dx.doi.org/10.1246/cl.1987.1379.

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28

Stojanović, Marija, Ljiljana Šćepanović, Olivera Bosnić, Dušan Mitrović, Olga Jozanov-Stankov, Vuk Šćepanović, Radomir Šćepanović, Teja Stojanović, Slobodan Ilić e Dragan Djurić. "Effects of Acute Administration of D,L-Homocysteine Thiolactone on the Antioxidative Status of Rat Intestine and Liver". Acta Veterinaria 66, n.º 1 (1 de março de 2016): 26–36. http://dx.doi.org/10.1515/acve-2016-0002.

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AbstractOxidative stress appears to play a role in the pathogenesis of several inflammatory gastrointestinal diseases. Increased homocysteine levels may play a role in the pathogenesis of Chron’s disease and ulcerative colitis. The aim of this study was to examine the influence of homocysteine on the antioxidant status of rat intestine and liver. The levels of thiobarbituric acid reactive substances (TBARS), activity of catalase (CAT) and total antioxidant status (TAS) were investigated in the isolated gut and liver of young male rats in the control group (8 rats) and after 3-hоur incubation in high doses of D, L-homocysteine thionolactone (Hcy) (10 μmol/L) (8 rats). Samples of duodenum, ileum, colon and liver were homogenized in sodium phosphate buffer (1:10). Homogenates were centrifuged at 10000 for 10 min at 4° C and the supernatant was taken for biochemical assays. Our results showed that high D, L-homocysteine thionolactone concentration reduced enzymatic catalase activity in homogenates of the isolated segments of duodenum (27.04%) p<0.01; ileum (37.27%), colon (34.17%) and liver (67.46%) p<0.001. Exposition to high D,L-homocysteine thiolactone concentration significantly increased TBARS levels in the duodenum (106.05%), ileum (47.24%), colon (112.75%) and liver (32.07%) (p<0.01). Homocysteine also modifi ed the total antioxidant status of homogenates from the duodenum, ileum, colon and liver, increasing by 20.68% (duodenum), 24.74% (ileum), 14.88% (colon) and 19.35% (liver) (p<0.001). Homocysteine induced a consistent oxidative stress in rat’s intestine and liver (reduced activity of catalase and increased level of TBARS), but the elevated activity of TAS in our experiments could be explained as an adaptive response to the generated free radicals which indicates the failure of the total antioxidant defense mechanism to protect the tissues from damage caused by homocysteine.

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29

Bringmann, G., B. Schöner, O. Schupp, W. A. Schenk, I. Reuther, K. Peters, E. M. Peters e H. G. von Schnering. "Synthesis and ring-opening reactions of cationic ruthenium biaryl thionolactone complexes". Journal of Organometallic Chemistry 472, n.º 1-2 (junho de 1994): 275–84. http://dx.doi.org/10.1016/0022-328x(94)80213-0.

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30

Iwasa, Seiji, Makoto Yamamoto, Shigeo Kohmoto e Kazutoshi Yamada. "Tandem radical cyclization of acyclic homoallylic xanthates: cyclopentannulated .gamma.-thionolactone and .gamma.-lactones". Journal of Organic Chemistry 56, n.º 8 (abril de 1991): 2849–53. http://dx.doi.org/10.1021/jo00008a048.

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31

IWASA, S., M. YAMAMOTO, S. KOHMOTO e K. YAMADA. "ChemInform Abstract: Tandem Radical Cyclization of Acyclic Homoallylic Xanthates: Cyclopentannulated γ-Thionolactone and γ-Lactones." ChemInform 22, n.º 41 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199141137.

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32

Peters, Karl, Eva-Maria Peters, Gerhard Bringmann e Olaf Schupp. "Notizen:1,3-Dimethoxy-6H- benzo[b]naphtho[1,2-d]pyran-6-thione, a Thionolactone-Bridged Axially Prostereogenic Biaryl". Zeitschrift für Naturforschung B 51, n.º 3 (1 de março de 1996): 431–32. http://dx.doi.org/10.1515/znb-1996-0320.

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Abstract The title compound was prepared from the corresponding “ordinary” oxolactone bridged biaryl using Lawesson’s reagent. It crystallizes from dichloromethane / petroleum ether in the monoclinic system, space group P21/a; a = 1115.7(2),b = 1383.9(2), c = 1042.0(1) pm and β = 106.67(1)°.

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33

Bringmann, Gerhard, Andreas Wuzik, Olaf Schupp, Karl Peters e Eva-Maria Peters. "1,3-Di-terf-butyl-6H-benzo[b]naphtho[1,2-d]pyran-6-thione, a Severely Helically Distorted Thionolactone-Bridged Biaryl". Zeitschrift für Naturforschung B 52, n.º 3 (1 de março de 1997): 355–58. http://dx.doi.org/10.1515/znb-1997-0310.

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Abstract The title compound 2c, a potentially useful synthetic intermediate in stereoselective biaryl synthesis, has been prepared from the oxolactone 1c, by treatment with Lawesson′s reagent. An X-ray structure analysis reveals its strongly helically distorted structure, the overall molecular distortion even slightly exceeding that of the corresponding oxo compound 1c.

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34

BRINGMANN, G., A. WUZIK, O. SCHUPP, K. PETERS e E. M. PETERS. "ChemInform Abstract: Novel Concepts in Direct Biaryl Synthesis. Part 60. 1,3-Di-tert-butyl- 6H-benzo(b)naphtho(1,2-d)pyran-6-thione, a Severely Helically Distorted Thionolactone-Bridged Biaryl." ChemInform 28, n.º 35 (3 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199735150.

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35

Chayajarus, Kampanart, e Antony J. Fairbanks. "Efficient Synthesis of Carbohydrate Thionolactones." ChemInform 37, n.º 35 (29 de agosto de 2006). http://dx.doi.org/10.1002/chin.200635209.

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36

Ivanchenko, Oleksandr, Stéphane Mazières, Rinaldo Poli, Simon Harrisson e Mathias Destarac. "Ring size-reactivity relationship in radical ring-opening copolymerisation of thionolactones with vinyl pivalate". Polymer Chemistry, 2022. http://dx.doi.org/10.1039/d2py01153k.

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The radical ring-opening copolymerisation (rROcoP) of unsubstituted thionolactones of different ring sizes, namely γ-thionobutyrolactone (TBL), δ-thionovalerolactone (TVL), ε-thionocaprolactone (TCL) and ω-thionopentadecalactone (TPDL), with vinyl pivalate has been mechanistically investigated. The...

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37

Wang, Wendong, Pornpun Rattananakin e Peter G. Goekjian. "Synthesis of N-Glycoside Analogues via Thionolactones." ChemInform 35, n.º 14 (6 de abril de 2004). http://dx.doi.org/10.1002/chin.200414226.

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38

"Organotin Hydride Catalyzed Radical Desulfurization of Thionoesters and Thionolactones". Synlett 2000, n.º 06 (2000): 0811–12. http://dx.doi.org/10.1055/s-2000-6723.

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39

Wilkinson, Brendan L., e Antony J. Fairbanks. "ChemInform Abstract: One-Pot Synthesis of Carbohydrate Thionolactones from 1-Thiosugars." ChemInform 39, n.º 47 (18 de novembro de 2008). http://dx.doi.org/10.1002/chin.200847198.

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40

Filippi, Jean-Jacques, Xavier Fernandez e Elisabet Dunach. "Lewis Acid Catalyzed Isomerization of Thionolactones to Thiolactones: Inversion of Configuration." ChemInform 37, n.º 48 (28 de novembro de 2006). http://dx.doi.org/10.1002/chin.200648125.

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41

Kalana, U. L. D. Inush, Partha P. Datta, Rukshika S. Hewawasam, Elizabeth T. Kiesewetter e Matthew K. Kiesewetter. "Organocatalytic ring-opening polymerization of thionolactones: anything O can do, S can do better". Polymer Chemistry, 2021. http://dx.doi.org/10.1039/d0py01393e.

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42

NICOLAOU, K. C., D. G. MCGARRY, P. K. SOMERS, B. H. KIM, W. W. OGILVIE, G. YIANNIKOUROS, C. V. C. PRASAD, C. A. VEALE e R. R. HARK. "ChemInform Abstract: Synthesis of Medium-Sized Ring Ethers from Thionolactones. Applications to Polyether Synthesis." ChemInform 21, n.º 49 (4 de dezembro de 1990). http://dx.doi.org/10.1002/chin.199049319.

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43

Ivanchenko, Oleksandr, Stéphane Mazières, Simon Harrisson e Mathias Destarac. "On-Demand Degradation of Thioester/Thioketal Functions in Vinyl Pivalate-Derived Copolymers with Thionolactones". Macromolecules, 1 de junho de 2023. http://dx.doi.org/10.1021/acs.macromol.3c00312.

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44

Rix, Matthew F. I., Kyle Collins, Samuel J. Higgs, Eleanor M. Dodd, Simon J. Coles, Nathaniel M. Bingham e Peter J. Roth. "Insertion of Degradable Thioester Linkages into Styrene and Methacrylate Polymers: Insights into the Reactivity of Thionolactones". Macromolecules, 30 de novembro de 2023. http://dx.doi.org/10.1021/acs.macromol.3c01811.

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45

NICOLAOU, K. C., D. G. MCGARRY, P. K. SOMERS, C. A. VEALE e G. T. FURST. "ChemInform Abstract: Nucleophilic Additions to Thionolactones. New Synthetic Technology for the Construction of Medium- and Large-Ring Ethers." ChemInform 18, n.º 35 (1 de setembro de 1987). http://dx.doi.org/10.1002/chin.198735251.

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46

BACHI, M. D., e E. BOSCH. "ChemInform Abstract: Free Radical Cyclization of Thionocarbonic Acid Derivatives of 4-Phenyl-3-butenol. A New Route to Thionolactones." ChemInform 20, n.º 35 (29 de agosto de 1989). http://dx.doi.org/10.1002/chin.198935184.

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47

Prebihalo, Emily A., Anna M. Luke, Yernaidu Reddi, Christopher J. LaSalle, Vijay M. Shah, Christopher J. Cramer e Theresa M. Reineke. "Radical ring-opening polymerization of sustainably-derived thionoisochromanone". Chemical Science, 2023. http://dx.doi.org/10.1039/d2sc06040j.

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We demonstrate computational insight and radical ring opening polymerization of a fungi-derived thionolactone, thionoisochromanone (TIC), to create homo-, block-, and statistical copolymers under entirely free radical conditions.

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48

TAKANO, S., S. TOMITA, M. TAKAHASHI e K. OGASAWARA. "ChemInform Abstract: Thionolactone Claisen Rearrangement." ChemInform 19, n.º 5 (2 de fevereiro de 1988). http://dx.doi.org/10.1002/chin.198805164.

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49

Elliss, Harry, Frances Dawson, Qamar un Nisa, Nathaniel M. Bingham, Peter J. Roth e Maciej Kopeć. "Fully Degradable Polyacrylate Networks from Conventional Radical Polymerization Enabled by Thionolactone Addition". Macromolecules, 25 de julho de 2022. http://dx.doi.org/10.1021/acs.macromol.2c01140.

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50

Lages, Maëlle, Noémie Gil, Paul Galanopoulo, Julie Mougin, Catherine Lefay, Yohann Guillaneuf, Muriel Lansalot, Franck D’Agosto e Julien Nicolas. "Degradable Latexes by Nitroxide-mediated Aqueous Seeded Emulsion Copolymerization Using a Thionolactone". Macromolecules, 20 de setembro de 2023. http://dx.doi.org/10.1021/acs.macromol.3c01478.

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