Relevant bibliographies by topics / Azidoketones

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Azidoketones'

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

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Journal articles on the topic "Azidoketones"

1

Wei, Wei, Huanhuan Cui, Huilan Yue та Daoshan Yang. "Visible-light-enabled oxyazidation of alkenes leading to α-azidoketones in air". Green Chemistry 20, № 14 (2018): 3197–202. http://dx.doi.org/10.1039/c8gc01245h.

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2

Van Sant, Karey, та Michael S. South. "Formation of α-enaminoketones from α-azidoketones: An elimination of molecular nitrogen from α-azidoketones". Tetrahedron Letters 28, № 48 (1987): 6019–20. http://dx.doi.org/10.1016/s0040-4039(00)96852-7.

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3

Chou, Chin-Hsing, Li-Tse Chu, I.-Ying Chen, and Bo-Jian Wu. "Pyrolytic Study of Cyclic 2-Azidoketones." HETEROCYCLES 75, no. 3 (2008): 577. http://dx.doi.org/10.3987/com-07-11239.

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4

Wang, Huey-Min, Rei-Sheu Hou, Jian-Long Wu та Ling-Ching Chen. "Polymer-Supported Hypervalent Iodine Reagent Mediated Synthesis of α-Azidoketones". Journal of the Chinese Chemical Society 54, № 5 (2007): 1333–35. http://dx.doi.org/10.1002/jccs.200700188.

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5

Yadav, J. S., B. V. Subba Reddy та M. Srinivas. "A Novel and Efficient Method for the Synthesis of α-Azidoketones and α-Ketothiocyanates". Chemistry Letters 33, № 7 (2004): 882–83. http://dx.doi.org/10.1246/cl.2004.882.

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6

Reddy, M. "A One Step Conversion of Olefins into α-Azidoketones using Azidotrimethylsilane-Chromium Trioxide Reagent System." Tetrahedron Letters 36, no. 3 (1995): 6751–54. http://dx.doi.org/10.1016/0040-4039(95)01332-c.

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7

Venkat Ram Reddy, M., R. Kumareswaran та Yashwant D. Vankar. "A one step conversion of olefins into α-Azidoketones using azidotrimethylsilane-chromium trioxide reagent system". Tetrahedron Letters 36, № 37 (1995): 6751–54. http://dx.doi.org/10.1016/00404-0399(50)1332-c.

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8

Langer, Peter, та Ilia Freifeld. "Efficient and regioselective synthesis of functionalized pyrroles by cyclocondensation of 1,3-dicarbonyl dianions with α-azidoketones". Chem. Commun., № 22 (2002): 2668–69. http://dx.doi.org/10.1039/b207840f.

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9

Marco, J. "Reaction of α-Azidoketones with Highly Stabilized Michael Acceptors: A New Synthesis of Densely Functionalized Pyrroles". Tetrahedron Letters 36, № 30 (1995): 5393–96. http://dx.doi.org/10.1016/00404-0399(50)0988o-.

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10

Chang, Ya-Li, Chi-Lin Chung, Fang-Wen Wu та ін. "Iodobenzene-Catalyzed Synthesis of α-Azidoketones and α-Thiocyanatoketones from Aryl Ketones with MCPBA as a Cooxidant". Journal of the Chinese Chemical Society 57, № 2 (2010): 149–52. http://dx.doi.org/10.1002/jccs.201000023.

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Dissertations / Theses on the topic "Azidoketones"

1

Wu, Jian-Long, та 吳建隆. "Ionic liquid promoted synthesis of α-azidoketones and quinoline derivatives". Thesis, 2007. http://ndltd.ncl.edu.tw/handle/16603925226947001269.

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碩士<br>高雄醫學大學<br>藥學研究所碩士班<br>95<br>Room temperature ionic liquids (RTIL) are liquids that are composed entirely of ions. In fact, ionic liquids can now be produced which remain liquid at room temperature and below (even as low as -90℃) and can be appeared to be undemanding and inexpensive to manufacture. Ionic liquids offer an attractive alterative to conventional organic liquids for clean synthesis, as they are recycling easily, lacking flammability, and possessing no vapour pressure effectively. Comparing with classical molecular solvents, the ionic liquids are environmentally benign reaction
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2

Chang, Ya-Li, and 張雅琍. "Hypervalent Iodine(III) Reagent Mediated Synthesis of Benzofurans, Imidazo[1,2-a]pyridines and a-Azidoketones." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/46710823878918386427.

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碩士<br>高雄醫學大學<br>藥學研究所<br>98<br>Recently, utilization of hypervalent iodine compounds in oxidative reactions has received great attention for their low toxicity compared with heavy metal oxidants, mild reaction conditions, special reactivity, and easy handling. In continuation of our efforts to develop greener organic reaction procedures, we report stoichiometric and catalytic oxidations with hypervalent iodine(III) reagent to prepare benzofurans, imidazo[1,2-a]pyridines and a-azidoketones. The method is simple, rapid and practical, the most valuable is benign to environment and generating targ
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3

Tichá, Iveta. "Využití B-H karbonátů v organokatalytických transformacích." Master's thesis, 2014. http://www.nusl.cz/ntk/nusl-333190.

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This diploma thesis is focused on the preparation of enantiomerically pure compounds based on organocatalytic allylic substitution using Baylis-Hillman carbonates. As selected substrates for the allylic substitution were chosen α-azidoketones such as azidoacetophenone, 2-azido-1-indanone and then heterocyclic compounds (N-phenylrhodanine and its derivate) belonging to the pharmaceutical privileged compounds. Other substrate for allylic substitution was allylmalononitrile. In addition, this thesis includes with synthesis of cyclic compounds based on the reaction of products of allylmalononitril
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