Literatura académica sobre el tema "Thiocarbonyl Group"
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Artículos de revistas sobre el tema "Thiocarbonyl Group"
Kirby, Christopher W., Michael D. Lumsden y Roderick E. Wasylishen. "A solid-state 13C NMR and theoretical investigation of carbonyl and thiocarbonyl carbon chemical shift tensors". Canadian Journal of Chemistry 73, n.º 4 (1 de abril de 1995): 604–13. http://dx.doi.org/10.1139/v95-078.
Texto completoMOLINA, M. T., M. YANEZ, O. MO, R. NOTARIO y J. L. M. ABBOUD. "ChemInform Abstract: The Thiocarbonyl Group". ChemInform 29, n.º 13 (23 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199813281.
Texto completoFernandez, José Manuel García y Carmen Ortiz Mellet. "The Thiocarbonyl Group in Carbohydrate Chemistry". Sulfur reports 19, n.º 1 (septiembre de 1996): 61–159. http://dx.doi.org/10.1080/01961779608047905.
Texto completoCorsaro, Antonino y Venerando Pistarà. "Conversion of the thiocarbonyl group into the carbonyl group". Tetrahedron 54, n.º 50 (diciembre de 1998): 15027–62. http://dx.doi.org/10.1016/s0040-4020(98)00880-1.
Texto completoCrich, David y Leticia Quintero. "Radical chemistry associated with the thiocarbonyl group". Chemical Reviews 89, n.º 7 (noviembre de 1989): 1413–32. http://dx.doi.org/10.1021/cr00097a001.
Texto completoKook Sohn, Chang, Eun Kyung Ma, Chang Kon Kim, Hai Whang Lee y Ikchoon Lee. "Theoretical studies on thiocarbonyl group transfer reactions". New Journal of Chemistry 25, n.º 6 (2001): 859–63. http://dx.doi.org/10.1039/b010202o.
Texto completoHuang, Chun-Hao, Pei-Jhen Wu, Kun-You Chung, Yi-An Chen, Elise Y. Li y Pi-Tai Chou. "Room-temperature phosphorescence from small organic systems containing a thiocarbonyl moiety". Physical Chemistry Chemical Physics 19, n.º 13 (2017): 8896–901. http://dx.doi.org/10.1039/c7cp00074j.
Texto completoAbram, Ulrich y Bernd Lorenz. "Thiocarbonyl Complexes of Rhenium. Part I." Zeitschrift für Naturforschung B 48, n.º 6 (1 de junio de 1993): 771–77. http://dx.doi.org/10.1515/znb-1993-0611.
Texto completoBarton, Derek H. R., Peter I. Dalko y Stephan D. Géro. "Radical cation reactions associated with the thiocarbonyl group". Tetrahedron Letters 33, n.º 14 (marzo de 1992): 1883–86. http://dx.doi.org/10.1016/s0040-4039(00)74167-0.
Texto completoGARCIA FERNANDEZ, J. M. y C. ORTIZ MELLET. "ChemInform Abstract: The Thiocarbonyl Group in Carbohydrate Chemistry". ChemInform 28, n.º 28 (3 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199728234.
Texto completoTesis sobre el tema "Thiocarbonyl Group"
Lin, Mei-Huei y 林浼憓. "A stereoselective glycosylation assisted by using thiocarbonyl as the auxiliary group". Thesis, 2018. http://ndltd.ncl.edu.tw/handle/f37j9b.
Texto completo國立臺灣科技大學
化學工程系
106
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 mechanism was clarified in low temperature NMR experiments, and phenyl thionocarbonyl group was applied to control high -selective glycosylation in wide disaccharide molecules.
CHANG, YA-JOU y 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.
Texto completo國立中正大學
化學暨生物化學研究所
108
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 influenced by preactivation time, because the different preactivation time may lead to the different ratio between the kinetic and thermodynamic intermediate. In this thesis,we designed three different functional group donors to study the relationship between preactivation time and stereoselectivity. The results showed that 3, 4-carbonyl and 3, 4-thiocarbonyl donor have the opposite trends of stereoselectivity with different preactivation time. Based on the experimental result, it could be suggested that the intermediate may affect the stereoselectivity. On the other hand, when different acceptors was glycosylated by 3, 4-thiocarbonyl galactoside with the different preactivation time, we could get various trends of stereoselectivity. According to this trends, acceptors could be classified to three types: high reactivity organic small molecule, high reactivity carbohydrate and poor reactivity carbohydrate.
Capítulos de libros sobre el tema "Thiocarbonyl Group"
Sato, S. y N. Furukawa. "Thiocarbonyl as Functional Group". En Four Carbon-Heteroatom Bonds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-01031.
Texto completoManyem, S. y M. P. Sibi. "Intramolecular Transfer of Sulfur from a Thiocarbonyl Group". En Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00531.
Texto completoBarluenga, José, Eduardo Rubio y Miguel Tomás. "Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other Than a Halogen or Chalcogen". En Comprehensive Organic Functional Group Transformations, 569–85. Elsevier, 1995. http://dx.doi.org/10.1016/b0-08-044705-8/00228-4.
Texto completoBarluenga, J., E. Rubio y M. Tomás. "Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other Than a Halogen or Chalcogen". En Comprehensive Organic Functional Group Transformations II, 545–72. Elsevier, 2005. http://dx.doi.org/10.1016/b0-08-044655-8/00139-2.
Texto completoKleinpeter, Erich y Kalevi Pihlaja. "Functions Containing a Thiocarbonyl Group and at Least One Halogen; Also at Least One Chalcogen and No Halogen". En Comprehensive Organic Functional Group Transformations, 527–67. Elsevier, 1995. http://dx.doi.org/10.1016/b0-08-044705-8/00273-9.
Texto completoKleinpeter, E. "Functions Containing a Thiocarbonyl Group and at Least One Halogen; Also at Least One Chalcogen and No Halogen". En Comprehensive Organic Functional Group Transformations II, 495–544. Elsevier, 2005. http://dx.doi.org/10.1016/b0-08-044655-8/00138-0.
Texto completoKantlehner, W. "Transformation of Carbonyl or Thiocarbonyl Groups into Methylene Groups". En Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00951.
Texto completoWakefield, Basil J. "Carbophilic Addition of Organomagnesium Compounds to Thiocarbonyl Groups". En Organomagnesium Methods in Organic Synthesis, 147–50. Elsevier, 1995. http://dx.doi.org/10.1016/b978-012730945-3.50009-8.
Texto completoTracey, M. R., R. P. Hsung, J. Antoline, K. C. M. Kurtz, L. Shen, B. W. Slafer y Y. Zhang. "Tungsten(0)-Mediated Coupling of Thiocarbonyl and Thioacetal Groups". En Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00392.
Texto completoHall, D. G. y H. Zheng. "Addition of Diboron Species to Carbonyl or Thiocarbonyl Groups, or Aldimines". En Boron Compounds, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-106-00011.
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