Academic literature on the topic 'Thionolactones'
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Journal articles on the topic "Thionolactones":
Chayajarus, Kampanart, and Antony J. Fairbanks. "Efficient synthesis of carbohydrate thionolactones." Tetrahedron Letters 47, no. 21 (May 2006): 3517–20. http://dx.doi.org/10.1016/j.tetlet.2006.03.104.
Iwasa, Seiji, Makoto Yamamoto, Shigeo Kohmoto, and Kazutoshi Yamada. "Synthesis of thionolactones from homoallylic xanthates." Journal of the Chemical Society, Perkin Transactions 1, no. 5 (1991): 1173. http://dx.doi.org/10.1039/p19910001173.
Wang, Wendong, Pornpun Rattananakin, and Peter G. Goekjian. "Synthesis of N‐Glycoside Analogs via Thionolactones." Journal of Carbohydrate Chemistry 22, no. 7-8 (December 31, 2003): 743–51. http://dx.doi.org/10.1081/car-120026472.
IWASA, S., M. YAMAMOTO, S. KOHMOTO, and K. YAMADA. "ChemInform Abstract: Synthesis of Thionolactones from Homoallylic Xanthates." ChemInform 22, no. 33 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199133165.
Wilkinson, Brendan L., and Antony J. Fairbanks. "One-pot synthesis of carbohydrate thionolactones from 1-thiosugars." Tetrahedron Letters 49, no. 33 (August 2008): 4941–43. http://dx.doi.org/10.1016/j.tetlet.2008.05.145.
Bringmann, Gerhard, Andreas Wuzik, Jörg Kümmel, and Wolfdieter A. Schenk. "Atropo-Enantioselective Ring Cleavage of Lewis Acid Modified Biaryl Thionolactones†,‡." Organometallics 20, no. 8 (April 2001): 1692–94. http://dx.doi.org/10.1021/om001040e.
Milewska, Maria J., Maria Gdaniec, and Tadeusz Poloński. "Synthesis, stereochemistry, and chiroptical spectra of cyclopropyl lactones and thionolactones." Tetrahedron: Asymmetry 7, no. 11 (November 1996): 3169–80. http://dx.doi.org/10.1016/0957-4166(96)00419-3.
Lee, Hyeon Kyu, Jia Kim, and Chwang Siek Pak. "Reaction of thionolactones with zinc enolate: new synthesis of vinylogous carbonates." Tetrahedron Letters 40, no. 34 (August 1999): 6267–70. http://dx.doi.org/10.1016/s0040-4039(99)01231-9.
Filippi, Jean-Jacques, Xavier Fernandez, and Elisabet Duñach. "Lewis acid-catalysed isomerisation of thionolactones to thiolactones: inversion of configuration." Tetrahedron Letters 47, no. 34 (August 2006): 6067–70. http://dx.doi.org/10.1016/j.tetlet.2006.06.104.
Beck, Thomas, and Armin Mosandl. "γ(δ)-Thionolactones - Enantioselective Capillary GC and Sensory Characteristics of Enantiomers." Journal of High Resolution Chromatography 22, no. 2 (February 1, 1999): 89–92. http://dx.doi.org/10.1002/(sici)1521-4168(19990201)22:2<89::aid-jhrc89>3.0.co;2-e.
Dissertations / Theses on the topic "Thionolactones":
Chayajarus, Kampanart. "The use of thioglycosides and thionolactones in glycoside synthesis." Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.432556.
Gil, Noémie. "Synthèse de polymères vinyliques dégradables par insertion de liaisons clivables : de la modélisation au matériau." Electronic Thesis or Diss., Aix-Marseille, 2022. http://www.theses.fr/2022AIXM0053.
The environmental impact caused by plastics is a major issue in recent years. Indeed, the persistence of this type of material creates many problems for flora, fauna and also for marine ecosystems. The polymers used in everyday life are, for the most part, derived from vinyl monomers, such as styrene or methyl (meth)acrylate. The polymers formed are composed exclusively of carbon-carbon bonds within their skeleton, which makes their degradability impossible. The aim of this thesis is to find a way to make everyday materials degradable while maintaining their properties. This is possible by using the comonomer approach which aims to add a cyclic comonomer (thionolactones), capable of copolymerization by radical ring-opening polymerization (rROP), allowing to insert cleavable functions within the polymer backbone. All these works have allowed to explore the potential and the limitations of thionolactones in radical ring-opening polymerization. For this purpose, different compounds will be synthesized and used in different formulations containing vinyl comonomers. The results obtained will be analyzed with the support of theoretical calculations (DFT calculations), allowing to better understand the polymerization mechanisms and finally to propose new optimized thionolactones which will be experimentally tested
Book chapters on the topic "Thionolactones":
Schenk, W. A., T. Beucke, J. Kümmel, F. Servatius, N. Sonnhalter, G. Bringmann, and A. Wuzik. "Stereo- and Enantioselective Reactions of Thioaldehydes, Thioketones, Thioketenes, and Thionolactones Mediated by Ruthenium Complexes." In Selective Reactions of Metal-Activated Molecules, 247–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-662-00975-8_37.
Wolf, Thomas, and Frederik R. Wurm. "Chapter 10. Organocatalytic Ring-opening Polymerization Towards Poly(cyclopropane)s, Poly(lactame)s, Poly(aziridine)s, Poly(siloxane)s, Poly(carbosiloxane)s, Poly(phosphate)s, Poly(phosphonate)s, Poly(thiolactone)s, Poly(thionolactone)s and Poly(thiirane)s." In Polymer Chemistry Series, 406–72. Cambridge: Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/9781788015738-00406.
Chemla, F., F. Ferreira, and B. Roy. "Synthesis from Thionolactones." In Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00739.