Relevant bibliographies by topics / Lawesson´s reagent

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Lawesson´s reagent'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Lawesson´s reagent"

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Preuss, Fritz, and Harald Noichl. "Oxo-und Thiovanadium(V)-Thiolate/Oxo and Thiovanadium(V) Thiolates." Zeitschrift für Naturforschung B 42, no. 2 (1987): 121–29. http://dx.doi.org/10.1515/znb-1987-0201.

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Abstract Syntheses of oxovanadium(V) thiolates such as O = V(SR)3 (R = tC4H9 , SiPh3 ) and O=V(OtC4H9 )n(StC4H9)3-n(n = 1, 2) are described. The thiovanadium(V) compounds S=V(OtC4H9 )3 , S = V(StC4H9)(OtC4H9) 2 and S=V(SSiPh3)3 have been prepared by various methods :substition using Lawesson reagent, oxidation of V(OtC4H9)4 by sulfur, or disproportionation reaction of VCl4 with LiSSiPh3 ; O = V (OSiR3)3 (R = Me , Ph) undergoes a reaction with Lawesson reagent to yield dithiophosphonate complexes. All compounds obtained are characterized by 1H and 51V NMR spectroscopy; the stability of thiovana
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Nizamov, Il'yas S., Alexey V. Matseevskii, Elvira S. Batyeva, Irina I. Vandyukova, Boris E. Abalonin, and Roald R. Shagidullin. "REACTIONS OF LAWESSON′S REAGENT WITH ARSENIC (III) ALKOXIDES." Phosphorus, Sulfur, and Silicon and the Related Elements 126, no. 1 (1997): 137–43. http://dx.doi.org/10.1080/10426509708043553.

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Aragoni, M. Carla, Massimiliano Arca, Alexander J. Blake, Vito Lippolis, Martin Schroeder, and Claire Wilson. "ChemInform Abstract: 4-Methoxyphenylphosphonic Acid: Reactivity of Lawesson′s Reagent." ChemInform 33, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.200238170.

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Osyanin, V. A., E. A. Ivleva, and Yu N. Klimochkin. "ChemInform Abstract: Reactions of 2-Hydroxymethylphenols with Lawesson′s Reagent." ChemInform 43, no. 17 (2012): no. http://dx.doi.org/10.1002/chin.201217186.

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Bringmann, Gerhard, Andreas Wuzik, Olaf Schupp, Karl Peters, and 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, no. 3 (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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He, Liang-Nian, Tian-Bao Huang, Fei Cai, and Ru-W. Chen. "STUDIES ON REACTIONS OF LAWESSON′S REAGENT WITH PHENYLTHIOUREA AND OXAMIDE." Phosphorus, Sulfur, and Silicon and the Related Elements 132, no. 1 (1998): 147–53. http://dx.doi.org/10.1080/10426509808036982.

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He, Liangnian, Yanping Luo, Kai Li, et al. "ChemInform Abstract: A Novel Route to Spiro Phosphorus-Heterocycle via Lawesson′s Reagent." ChemInform 33, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.200239174.

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Red'kin, V. M., T. A. Stroganova, V. K. Vasilin, and G. D. Krapivin. "ChemInform Abstract: Reaction of Vicinal Thieno[2,3-b]pyridine Aminoamides with Lawesson′s Reagent." ChemInform 44, no. 34 (2013): no. http://dx.doi.org/10.1002/chin.201334181.

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Nishio, Takehiko, Norikazu Okuda, Yo-ichi Mori, and Choji Kashima. "Reaction of 3-Hydroxyisoindolin-1-ones with Lawesson Reagent. Synthesis of Isoindoline-1-thiones." Synthesis 1989, no. 05 (1989): 396–97. http://dx.doi.org/10.1055/s-1989-27264.

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Shabana, R., L. S. Boulos, and Y. M. Shaker. "ChemInform Abstract: Organophosphorus Compounds. Part 18. The Reaction of Lawesson′s Reagent with Trihydroxy Compounds." ChemInform 30, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.199919187.

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Dissertations / Theses on the topic "Lawesson´s reagent"

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Mingle, David. "Synthesis, Characterization and Biological Evaluation of Novel (S,E)-11-[2-(Arylmethylene) Hydrazono] Pyrrolo [2,1-c] [1,4] Benzodiazepine Derivatives." Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/etd/3596.

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Pyrrolo [2,1-c] [1,4] benzodiazepine (PBD) is a class of natural products obtained from various actinomycetes which have both anti-tumor and antibiotic activities and can bind to specific sequences of DNA. PBD-dilactam was initially produced using isatoic anhydride and (L)-proline which was then converted to the PBD-thiolactam using Lawesson's reagent. Reaction of thiolactam with hydrazine in ethanol afforded PBD-11-hydrazinyl. Condensation of 11-hydrazinyl PBD with aldehydes possessing various substitutions was performed to obtain (S,E)-11-[2-(arylmethylene) hydrazono] pyrrolo [2,1-c] [1,4] b
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Shin, Younghun. "Modifying naphthalene diimide copolymers for applications in thermoelectric devices." 2020. https://monarch.qucosa.de/id/qucosa%3A71753.

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The aim of this thesis is to modify and improve the n-type semiconducting polymer PNDIT2 for thermoelectric generators (TEGs) applications. Although the PNDIT2 is considered a prime n-type material due to its high electron mobility, low air-stability of radical anions after doping and the low doping efficiency with molecular dopants are severe drawbacks and lead to limited application in TEGs. To this end, the backbone structure of PNDIT2 is modified by polymer analogous thionation and the branched aliphatic side chains are replaced by branched, fully oligoethylene glycol-based side chains. PN
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Book chapters on the topic "Lawesson´s reagent"

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Kaur, Navjeet. "S-Heterocycle Synthesis." In Lawesson’s Reagent in Heterocycle Synthesis. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4655-3_6.

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Kaur, Navjeet. "Five-Membered S-Heterocycle Synthesis." In Lawesson’s Reagent in Heterocycle Synthesis. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4655-3_5.

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Kaur, Navjeet. "Thiazole Synthesis by Thionation of C=O to C=S." In Lawesson’s Reagent in Heterocycle Synthesis. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4655-3_3.

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Conference papers on the topic "Lawesson´s reagent"

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Montaño, Rocío, and Murali Venkata Unnamatla. "Efficient and rapid conversion of 3-amino imidazo[1,2-a] pyridin-2-yl)-4H-chromene-4-ones to its corresponding thio analogues using Lawesson’s reagent ." In The 22nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecsoc-22-05668.

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You might also be interested in the extended bibliographies on the topic 'Lawesson´s reagent' for particular source types:
Journal articles
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