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Relevant bibliographies by topics / Thiocarbonyl Group

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Journal articles
Dissertations / Theses
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Academic literature on the topic 'Thiocarbonyl Group'

Author: Grafiati

Published: 6 September 2023

Last updated: 31 July 2025

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Journal articles on the topic "Thiocarbonyl Group"

1

Kirby, Christopher W., Michael D. Lumsden, and Roderick E. Wasylishen. "A solid-state 13C NMR and theoretical investigation of carbonyl and thiocarbonyl carbon chemical shift tensors." Canadian Journal of Chemistry 73, no. 4 (1995): 604–13. http://dx.doi.org/10.1139/v95-078.

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The carbon chemical shift tensors of the carbonyl and thiocarbonyl groups of acetamide, thioacetamide, thioacetanilide, 4′-methoxyacetanilide, and 4′-methoxythioacetanilide have been experimentally determined using dipolar – chemical shift solid-state 13C NMR spectroscopy. The magnitudes of the three principal components of the carbon chemical shift tensors are found to exhibit marked variations between the carbonyl and thiocarbonyl functionalities. However, in contrast to the conclusions of an earlier comparative investigation involving benzophenone and thiobenzophenone, the orientations of t

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2

MOLINA, M. T., M. YANEZ, O. MO, R. NOTARIO, and J. L. M. ABBOUD. "ChemInform Abstract: The Thiocarbonyl Group." ChemInform 29, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199813281.

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3

Fernandez, José Manuel García, and Carmen Ortiz Mellet. "The Thiocarbonyl Group in Carbohydrate Chemistry." Sulfur reports 19, no. 1 (1996): 61–159. http://dx.doi.org/10.1080/01961779608047905.

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4

Corsaro, Antonino, and Venerando Pistarà. "Conversion of the thiocarbonyl group into the carbonyl group." Tetrahedron 54, no. 50 (1998): 15027–62. http://dx.doi.org/10.1016/s0040-4020(98)00880-1.

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5

Crich, David, and Leticia Quintero. "Radical chemistry associated with the thiocarbonyl group." Chemical Reviews 89, no. 7 (1989): 1413–32. http://dx.doi.org/10.1021/cr00097a001.

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6

Kook Sohn, Chang, Eun Kyung Ma, Chang Kon Kim, Hai Whang Lee, and Ikchoon Lee. "Theoretical studies on thiocarbonyl group transfer reactions." New Journal of Chemistry 25, no. 6 (2001): 859–63. http://dx.doi.org/10.1039/b010202o.

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7

Huang, Chun-Hao, Pei-Jhen Wu, Kun-You Chung, Yi-An Chen, Elise Y. Li, and Pi-Tai Chou. "Room-temperature phosphorescence from small organic systems containing a thiocarbonyl moiety." Physical Chemistry Chemical Physics 19, no. 13 (2017): 8896–901. http://dx.doi.org/10.1039/c7cp00074j.

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8

Abram, Ulrich, and Bernd Lorenz. "Thiocarbonyl Complexes of Rhenium. Part I." Zeitschrift für Naturforschung B 48, no. 6 (1993): 771–77. http://dx.doi.org/10.1515/znb-1993-0611.

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Novel rhenium complexes with terminal thiocarbonyl groups have been synthesized from ReCl3(Me2PhP)3 and sodium diethyldithiocarbamate. mer-(Diethyldithiocarbamato)tris-(dimethylphenylphosphine)(thiocarbonyl)rhenium(I), mer-[Re(CS)(Me2PhP)3(Et2dtc)], and tris(diethyldithiocarbamato)(thiocarbonyl)rhenium(III), [Re(CS)(Et2dtc)3] have been studied by infrared and NMR spectroscopy, mass spectrometry and X-ray diffraction.mer-[Re(CS)(Me2PhP)3(Et2dtc)] crystallizes orthorhombic in the space group Pna21 with a = 1516.1(2), b = 2189.8(2) and c = 1035.6(1) pm. Structure solution and refinement converged

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9

Gouran, Ali Asghar, and Sakineh Asghari. "On Searching for a Stepwise Channel for the Mechanism of a 1,3-Dipolar Cycloaddition between a Thiocarbonyl S-Oxide and C20 Fullerene using Born–Oppenheimer ab Initio QM/MM Molecular Dynamics." Progress in Reaction Kinetics and Mechanism 42, no. 3 (2017): 282–88. http://dx.doi.org/10.3184/146867817x14954764850315.

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The probability of existence of a stepwise route which is in parallel with the well-known concerted pathway for the mechanism of 1,3-dipolar cycloaddition is debated by many researchers. As the route is stepwise, it would lead to emergence of at least a metastable intermediate which would produce some stereoisomers such as enantiomers and diastereomers. In 1986 the first clear stepwise example for a 1,3-dipolar cycloaddition was reported by Huisgen where an electron-poor alkene was reacted with a thiocarbonyl ylide. Since then, researchers have focused on the thiocarbonyl ylide 1,3-dipolar gro

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10

Reepmeyer, John C., and D. Andr d'Avignon. "Use of a Hydrolytic Procedure and Spectrometric Methods in the Structure Elucidation of a Thiocarbonyl Analogue of Sildenafil Detected as an Adulterant in an Over-the-Counter Herbal Aphrodisiac." Journal of AOAC INTERNATIONAL 92, no. 5 (2009): 1336–42. http://dx.doi.org/10.1093/jaoac/92.5.1336.

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Abstract A sildenafil-related compound was detected in an herbal dietary supplement marketed as an aphrodisiac. The compound was identified as an analogue of sildenafil in which the carbonyl group in the pyrimidine ring of sildenafil was substituted with a thiocarbonyl group, and the methyl group on the piperazine ring was substituted with a hydroxyethyl group. Based on this structure, the compound was named thiohydroxyhomosildenafil. The structure of the compound was established using HPLC/MS, UV spectrometry, electrospray ionization-MS/MS, NMR spectrometry, and a hydrolytic process. One key

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Dissertations / Theses on the topic "Thiocarbonyl Group"

1

Reddy, K. V. "A) Nitrothioacetamides: synthesis and chemical transformations; B) Study of some weak interactions of the thiocarbonyl group." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1992. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3912.

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Lin, Mei-Huei, and 林浼憓. "A stereoselective glycosylation assisted by using thiocarbonyl as the auxiliary group." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/f37j9b.

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碩士<br>國立臺灣科技大學<br>化學工程系<br>106<br>Deoxy sugar is a core structure dominating an important role in living organisms. However, the mechanism is still unclear because of low yield and poor selectivity in organic synthesis. To achieve these challenges, a one pot synthetic strategy was established by using phenyl thionocarbonyl group. First, with a single step, the phenoxythiocarbonyl donor, a precursor of deoxy sugar, was obtained in high yield. Secondly, phenoxythiocarbonyl donor was employed to achieve stereoselective glycosylation by using neighboring group participation. Finally, the reaction

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3

CHANG, YA-JOU, and 張雅柔. "The Development of Preactivation Time-Dependent Stereoselective Glycosylation Reaction with 3, 4-Thiocarbonyl Group." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/49z5ju.

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碩士<br>國立中正大學<br>化學暨生物化學研究所<br>108<br>The carbohydrates play an important role in bio-organism. They not only provide and store energy for daily activities, but also regulate many physiological functions with the others biomolecule on cell surface. To further study the mechanism of carbohydrates in organisms, making a correct stereoselectivity compound during synthesizing is an important work. In the way of organic synthesis, it can be divided to two methods depending on the order of adding activated reagent, one is nonpreactivation, the other is preactivation. The stereoselectivity may be infl

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Book chapters on the topic "Thiocarbonyl Group"

1

Sato, S., and N. Furukawa. "Thiocarbonyl as Functional Group." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-01031.

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2

Manyem, S., and M. P. Sibi. "Intramolecular Transfer of Sulfur from a Thiocarbonyl Group." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00531.

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3

Barluenga, José, Eduardo Rubio, and Miguel Tomás. "Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other Than a Halogen or Chalcogen." In Comprehensive Organic Functional Group Transformations. Elsevier, 1995. http://dx.doi.org/10.1016/b0-08-044705-8/00228-4.

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4

Davies, David T. "Answers to problems." In Aromatic Heterocyclic Chemistry. Oxford University Press, 1992. http://dx.doi.org/10.1093/hesc/9780198556602.003.0011.

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This chapter presents the answers to the problems included in the previous chapters. Reaction of diketone with aminoketone produces enamine, which is not isolated, but cyclinizes directly to give pyrrole. Meanwhile, the application of generalised oxazole retrosynthesis leads to a simple glycine derivative. The mechanism of the oxazole formation is identical to that of the Hantzch thiazole synthesis. However, because of the reduced nucleophilicity of a carbonyl group as compared to a thiocarbonyl, this synthesis only proceeds under vigorous conditions. The alternative sequence would give a posi

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Barluenga, J., E. Rubio, and M. Tomás. "Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other Than a Halogen or Chalcogen." In Comprehensive Organic Functional Group Transformations II. Elsevier, 2005. http://dx.doi.org/10.1016/b0-08-044655-8/00139-2.

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Kleinpeter, Erich, and Kalevi Pihlaja. "Functions Containing a Thiocarbonyl Group and at Least One Halogen; Also at Least One Chalcogen and No Halogen." In Comprehensive Organic Functional Group Transformations. Elsevier, 1995. http://dx.doi.org/10.1016/b0-08-044705-8/00273-9.

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Kleinpeter, E. "Functions Containing a Thiocarbonyl Group and at Least One Halogen; Also at Least One Chalcogen and No Halogen." In Comprehensive Organic Functional Group Transformations II. Elsevier, 2005. http://dx.doi.org/10.1016/b0-08-044655-8/00138-0.

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8

Kantlehner, W. "Transformation of Carbonyl or Thiocarbonyl Groups into Methylene Groups." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00951.

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9

Wakefield, Basil J. "Carbophilic Addition of Organomagnesium Compounds to Thiocarbonyl Groups." In Organomagnesium Methods in Organic Synthesis. Elsevier, 1995. http://dx.doi.org/10.1016/b978-012730945-3.50009-8.

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10

Tracey, M. R., R. P. Hsung, J. Antoline, et al. "Tungsten(0)-Mediated Coupling of Thiocarbonyl and Thioacetal Groups." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00392.

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