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Journal articles on the topic 'Azidoketones'

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

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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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11

MARCO, J. L., A. MARTINEZ-GRAU, N. MARTIN та C. SEOANE. "ChemInform Abstract: Reaction of α-Azidoketones with Highly Stabilized Michael Acceptors: A New Synthesis of Densely Functionalized Pyrroles." ChemInform 26, № 44 (2010): no. http://dx.doi.org/10.1002/chin.199544123.

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12

Yadav, J. S., P. Thirupathi Reddy, S. Nanda, and A. Bhaskar Rao. "Stereoselective synthesis of (R)-(−)-denopamine, (R)-(−)-tembamide and (R)-(−)-aegeline via asymmetric reduction of azidoketones by Daucus carota in aqueous medium." Tetrahedron: Asymmetry 12, no. 24 (2002): 3381–85. http://dx.doi.org/10.1016/s0957-4166(02)00024-1.

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13

REDDY, M. V. R., R. KUMARESWARAN та Y. D. VANKAR. "ChemInform Abstract: General Synthetic Methods. Part 3. A One-Step Conversion of Olefins into α-Azidoketones Using Azidotrimethylsilane-Chromium Trioxide Reagent System." ChemInform 26, № 52 (2010): no. http://dx.doi.org/10.1002/chin.199552100.

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14

Freifeld, Ilia, Heydar Shojaei та Peter Langer. "Synthesis of 2-Alkylidenepyrrolidines and Pyrroles by Condensation of 1,3-Dicarbonyl Dianions with α-Azidoketones and Subsequent Intramolecular Staudinger−Aza-Wittig Reaction". Journal of Organic Chemistry 71, № 13 (2006): 4965–68. http://dx.doi.org/10.1021/jo060593h.

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15

Yadav, J. S., P. Thirupathi Reddy, S. Nanda, and A. Bhaskar Rao. "ChemInform Abstract: Stereoselective Synthesis of (R)-(-)-Denopamine, (R)-(-)-Tembamide, and (R)-(-)-Aegeline via Asymmetric Reduction of Azidoketones by Daucus carota in Aqueous Medium." ChemInform 33, no. 34 (2010): no. http://dx.doi.org/10.1002/chin.200234260.

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16

Chandra, Ajeet, Keshaba Nanda Parida та Jarugu Narasimha Moorthy. "One-pot synthesis of α-bromo- and α-azidoketones from olefins by catalytic oxidation with in situ-generated modified IBX as the key reaction". Tetrahedron 73, № 40 (2017): 5827–32. http://dx.doi.org/10.1016/j.tet.2017.08.019.

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17

Varma, Rajender S., Kannan P. Naicker та Dalip Kumar. "Can ultrasound substitute for a phase-transfer catalyst? Triphase catalysis and sonochemical acceleration in nucleophilic substitution of alkyl halides and α-tosyloxyketones: synthesis of alkyl azides and α-azidoketones". Journal of Molecular Catalysis A: Chemical 149, № 1-2 (1999): 153–60. http://dx.doi.org/10.1016/s1381-1169(99)00168-5.

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18

Kumar, Dalip, Swapna Sundaree та V. S. Rao. "Facile One‐Step Conversion of Ketones into α‐Azidoketones using [Hydroxy(tosyloxy)iodo]benzene and Sodium Azide in the Presence of a Phase‐Transfer Catalyst under Solvent‐Free Conditions". Synthetic Communications 36, № 13 (2006): 1893–96. http://dx.doi.org/10.1080/00397910600602644.

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19

Procopiou, Panayiotis A., Gillian E. Morton, Martin Todd, and Graham Webb. "Enantioselective synthesis of (S)-salmeterol via asymmetric reduction of azidoketone by Pichia angusta." Tetrahedron: Asymmetry 12, no. 14 (2001): 2005–8. http://dx.doi.org/10.1016/s0957-4166(01)00350-0.

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20

Effenberger, Franz, Thomas Beisswenger, and Rainer Az. "Zersetzung von 2-Azidoketonen zu 2-(Acetylamino)-2-alken-1-onen unter Perrhenat-Katalyse." Chemische Berichte 118, no. 12 (1985): 4869–76. http://dx.doi.org/10.1002/cber.19851181221.

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21

Chou, Chin-Hsing, Li-Tse Chu, I.-Ying Chen, and Bo-Jian Wu. "ChemInform Abstract: Pyrolytic Study of Cyclic 2-Azidoketones." ChemInform 39, no. 26 (2008). http://dx.doi.org/10.1002/chin.200826030.

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22

VAULTIER, M., P. H. LAMBERT та R. CARRIE. "ChemInform Abstract: Reaction of ω-Azidoketones with Triphenylphosphine: General Approach to Cyclic Imines." Chemischer Informationsdienst 17, № 27 (1986). http://dx.doi.org/10.1002/chin.198627096.

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23

Yadav, J. S., V. B. Subba Reddy та M. Srinivas. "A Novel and Efficient Method for the Synthesis of α-Azidoketones and α-Ketothiocyanates." ChemInform 35, № 49 (2004). http://dx.doi.org/10.1002/chin.200449050.

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24

Langer, Peter, та Ilia Freifeld. "Efficient and Regioselective Synthesis of Functionalized Pyrroles by Cyclocondensation of 1,3-Dicarbonyl Dianions with α-Azidoketones." ChemInform 34, № 12 (2003). http://dx.doi.org/10.1002/chin.200312108.

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25

"Efficient Preparations of α-Azidoketones and α-Thiocyanatoketones via α-Sulfonyloxy Aryl Ketone Intermediates in Ionic Liquid". Bulletin of the Korean Chemical Society 26, № 10 (2005): 1493–94. http://dx.doi.org/10.5012/bkcs.2005.26.10.1493.

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26

Kumar, Anil, Israr Ahmed, M. Sudershan Rao, Gautam Patel та Dalip Kumar. "ChemInform Abstract: A Simple and Efficient PTT-Mediated Synthesis of α-Azidoketones in [bmim][BF4] Ionic Liquid." ChemInform 40, № 31 (2009). http://dx.doi.org/10.1002/chin.200931042.

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27

Lee, Jong Chan, та Jin Seo Lee. "Efficient Preparations of α-Azidoketones and α-Thiocyanatoketones via α-Sulfonyloxy Aryl Ketone Intermediates in Ionic Liquid." ChemInform 37, № 10 (2006). http://dx.doi.org/10.1002/chin.200610105.

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28

Freifeld, Ilia, Heydar Shojaei та Peter Langer. "Synthesis of 2-Alkylidenepyrrolidines and Pyrroles by Condensation of 1,3-Dicarbonyl Dianions with α-Azidoketones and Subsequent Intramolecular Staudinger—Aza-Wittig Reaction." ChemInform 37, № 45 (2006). http://dx.doi.org/10.1002/chin.200645102.

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29

Kumar, Dalip, Swapna Sundaree та V. S. Rao. "Facile One-Step Conversion of Ketones into α-Azidoketones Using [Hydroxy(tosyloxy)iodo]benzene and Sodium Azide in the Presence of a Phase-Transfer Catalyst under Solvent-Free Conditions." ChemInform 37, № 45 (2006). http://dx.doi.org/10.1002/chin.200645063.

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