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Journal articles on the topic 'Liebeskind-Srogl'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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1

Schaaf, Patricia, Thomas Bayer, Moumita Koley, et al. "Biocompatible metal-assisted C–C cross-coupling combined with biocatalytic chiral reductions in a concurrent tandem cascade." Chemical Communications 54, no. 92 (2018): 12978–81. http://dx.doi.org/10.1039/c8cc05304a.

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We present a concurrent chemo/biocatalytic one pot reaction cascade by combining a metal (Pd/Cu) assisted Liebeskind–Srogl coupling with an enantioselective enzymatic reduction for the production of chiral amines and alcohols.

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2

Yang, Quanlu, Zhengjun Quan, Baoxin Du, et al. "Wool-anchored Pd(OAc)2 complex: a highly active and reusable catalyst for desulfurative coupling reactions." Catalysis Science & Technology 5, no. 9 (2015): 4522–31. http://dx.doi.org/10.1039/c5cy00802f.

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A biomacromolecule-anchored palladium complex, wool-Pd(OAc)<sub>2</sub>, was used as a catalyst for the Liebeskind–Srogl desulfurative coupling reactions of pyrimidin-yl thioether derivatives with terminal alkynes and arylboronic acids.

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3

Dandepally, Srinivasa Reddy, and Alfred L. Williams. "Liebeskind–Srogl cross coupling mediated synthesis of verbenachalcone." Tetrahedron Letters 51, no. 44 (2010): 5753–56. http://dx.doi.org/10.1016/j.tetlet.2010.08.073.

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4

Prokopcová, Hana, and C. Oliver Kappe. "Die C-C-Kreuzkupplung nach Liebeskind und Srogl." Angewandte Chemie 121, no. 13 (2009): 2312–22. http://dx.doi.org/10.1002/ange.200802842.

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5

Prokopcová, Hana, and C. Oliver Kappe. "The Liebeskind-Srogl CC Cross-Coupling Reaction." Angewandte Chemie International Edition 48, no. 13 (2008): 2276–86. http://dx.doi.org/10.1002/anie.200802842.

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6

Ma, Yuanhong, Jose Cammarata, and Josep Cornella. "Ni-Catalyzed Reductive Liebeskind–Srogl Alkylation of Heterocycles." Journal of the American Chemical Society 141, no. 5 (2019): 1918–22. http://dx.doi.org/10.1021/jacs.8b13534.

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7

Piqani, Bruno, and Wei Zhang. "Synthesis of diverse dihydropyrimidine-related scaffolds by fluorous benzaldehyde-based Biginelli reaction and post-condensation modifications." Beilstein Journal of Organic Chemistry 7 (September 16, 2011): 1294–98. http://dx.doi.org/10.3762/bjoc.7.150.

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Dihydropyrimidinones and dihydropyrimidinethiones generated from the Biginelli reactions of perfluorooctanesulfonyl-attached benzaldehydes are used as common intermediates for post-condensation modifications such as cycloaddition, Liebeskind–Srogl reaction and Suzuki coupling to form biaryl-substituted dihydropyrimidinone, dihydropyrimidine, and thiazolopyrimidine compounds. The high efficiency of the diversity-oriented synthesis is achieved by conducting a multicomponent reaction for improved atom economy, under microwave heating for fast reaction, and with fluorous solid-phase extractions (F

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8

Sun, Qi, Franck Suzenet, and Gérald Guillaumet. "Optimized Liebeskind–Srogl coupling reaction between dihydropyrimidines and tributyltin compounds." Tetrahedron Letters 53, no. 22 (2012): 2694–98. http://dx.doi.org/10.1016/j.tetlet.2012.03.067.

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9

Fujii, Tomohiro, Yuta Oki, and Masahisa Nakada. "Research on Liebeskind-Srogl coupling/intramolecular Diels-Alder reaction cascade." Tetrahedron Letters 59, no. 10 (2018): 882–86. http://dx.doi.org/10.1016/j.tetlet.2018.01.046.

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10

Han, Junyan, Oswaldo Gonzalez, Angelica Aguilar-Aguilar, Eduardo Peña-Cabrera, and Kevin Burgess. "3- and 5-Functionalized BODIPYs via the Liebeskind-Srogl reaction." Org. Biomol. Chem. 7, no. 1 (2009): 34–36. http://dx.doi.org/10.1039/b818390b.

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11

Cheng, Hong-Gang, Han Chen, Yue Liu, and Qianghui Zhou. "The Liebeskind-Srogl Cross-Coupling Reaction and its Synthetic Applications." Asian Journal of Organic Chemistry 7, no. 3 (2018): 490–508. http://dx.doi.org/10.1002/ajoc.201700651.

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12

Tatibouët, Arnaud, Sandrine Gosling, and Patrick Rollin. "Thiohydantoins: Selective N- and S-Functionalization for Liebeskind-Srogl Reaction Study." Synthesis 2011, no. 22 (2011): 3649–60. http://dx.doi.org/10.1055/s-0030-1260259.

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13

Sun, Qi, Franck Suzenet, and Gerald Guillaumet. "ChemInform Abstract: Optimized Liebeskind-Srogl Coupling Reaction Between Dihydropyrimidines and Tributyltin Compounds." ChemInform 43, no. 36 (2012): no. http://dx.doi.org/10.1002/chin.201236164.

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14

Kappe, C., Hana Prokopcová, and Leonardo Pisani. "Synthesis of 5-Aroyldihydropyrimidinones via Liebeskind-Srogl Thiol Ester-Boronic Acid Cross-Couplings." Synlett 2007, no. 1 (2007): 0043–46. http://dx.doi.org/10.1055/s-2006-958443.

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15

Lambert, William D., Yinzhi Fang, Subham Mahapatra, Zhen Huang, Christopher W. am Ende, and Joseph M. Fox. "Installation of Minimal Tetrazines through Silver-Mediated Liebeskind–Srogl Coupling with Arylboronic Acids." Journal of the American Chemical Society 141, no. 43 (2019): 17068–74. http://dx.doi.org/10.1021/jacs.9b08677.

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16

Betancourt-Mendiola, Lourdes, Ismael Valois-Escamilla, Teresa Arbeloa, et al. "Scope and Limitations of the Liebeskind–Srogl Cross-Coupling Reactions Involving the Biellmann BODIPY." Journal of Organic Chemistry 80, no. 11 (2015): 5771–82. http://dx.doi.org/10.1021/acs.joc.5b00731.

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17

Kokate, Siddhant V., Angélica Aguilar-Aguilar, Miguel A. Vázquez-Guevara, Gabriel Luna-Bárcenas, Alejandro J. Gimenez, and Eduardo Peña-Cabrera. "Synthesis bis-thienyl-substituted cyclobutenedione via the Liebeskind-Srogl and Stille cross-coupling reactions." Arkivoc 2021, no. 3 (2021): 76–84. http://dx.doi.org/10.24820/ark.5550190.p011.459.

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18

Pérez-Venegas, Mario, Miriam N. Villanueva-Hernández, Eduardo Peña-Cabrera, and Eusebio Juaristi. "Mechanochemically Activated Liebeskind–Srogl (L-S) Cross-Coupling Reaction: Green Synthesis of meso-Substituted BODIPYs." Organometallics 39, no. 14 (2020): 2561–64. http://dx.doi.org/10.1021/acs.organomet.0c00037.

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19

Břehová, Petra, Michal Česnek, Martin Dračínský, Antonín Holý, and Zlatko Janeba. "The efficient synthesis of 2-arylpyrimidine acyclic nucleoside phosphonates using Liebeskind–Srogl cross-coupling reaction." Tetrahedron 67, no. 38 (2011): 7379–85. http://dx.doi.org/10.1016/j.tet.2011.07.040.

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20

Tsuna, Kazuhiro, Naoyoshi Noguchi, and Masahisa Nakada. "Synthesis of medium-sized carbocyclic ketones via the intramolecular B-alkyl Liebeskind–Srogl coupling reaction." Tetrahedron Letters 52, no. 52 (2011): 7202–5. http://dx.doi.org/10.1016/j.tetlet.2011.10.148.

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21

Ábrányi-Balogh, Péter, Péter Slégel, Balázs Volk, László Pongó, and Mátyás Milen. "New Synthetic Approach for the Preparation of 1-Aryl-3,4-dihydroisoquinolines by Liebeskind–Srogl Reaction." Synlett 25, no. 18 (2014): 2574–78. http://dx.doi.org/10.1055/s-0034-1379109.

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22

Aguilar-Aguilar, Angélica, and Eduardo Peña-Cabrera. "Selective Cross-Couplings. Sequential Stille−Liebeskind/Srogl Reactions of 3-Chloro-4-arylthiocyclobutene-1,2-dione." Organic Letters 9, no. 21 (2007): 4163–66. http://dx.doi.org/10.1021/ol701628z.

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23

Murata, Yuki, Aki Terazoe, Misato Kiba, Yuki Kitamura, Mio Matsumura, and Shuji Yasuike. "Liebeskind-Srogl-type cross-coupling reaction of azole-2-thiones with triarylbismuthines: Synthesis of 2-arylazoles." Tetrahedron Letters 61, no. 30 (2020): 152152. http://dx.doi.org/10.1016/j.tetlet.2020.152152.

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24

Pena-Cabrera, Eduardo, and et al. "ChemInform Abstract: Scope and Limitations of the Liebeskind-Srogl Cross-Coupling Reactions Involving the Biellmann BODIPY." ChemInform 46, no. 43 (2015): no. http://dx.doi.org/10.1002/chin.201543053.

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25

Abranyi-Balogh, Peter, Peter Slegel, Balazs Volk, Laszlo Pongo, and Matyas Milen. "ChemInform Abstract: New Synthetic Approach for the Preparation of 1-Aryl-3,4-dihydroisoquinolines by Liebeskind-Srogl Reaction." ChemInform 46, no. 17 (2015): no. http://dx.doi.org/10.1002/chin.201517212.

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26

Brehova, Petra, Michal Cesnek, Martin Dracinsky, Antonin Holy, and Zlatko Janeba. "ChemInform Abstract: The Efficient Synthesis of 2-Arylpyrimidine Acyclic Nucleoside Phosphonates Using Liebeskind-Srogl Cross-Coupling Reaction." ChemInform 43, no. 6 (2012): no. http://dx.doi.org/10.1002/chin.201206200.

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27

Peng, Yang-Qiu, Lai-Chun Luo, Jiao Gong, Jian Huang, and Qi Sun. "New synthetic approach for the preparation of 2-aryl-thiazolo[4,5-b]pyridines via Liebeskind–Srogl reaction." Chinese Chemical Letters 26, no. 8 (2015): 1016–18. http://dx.doi.org/10.1016/j.cclet.2015.05.012.

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28

Fenneteau, Johan, Sara Vallerotto, Laurent Ferrié та Bruno Figadère. "Liebeskind–Srogl cross-coupling on γ-carboxyl-γ-butyrolactone derivatives: application to the side chain of amphidinolides C and F". Tetrahedron Letters 56, № 24 (2015): 3758–61. http://dx.doi.org/10.1016/j.tetlet.2015.04.035.

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29

Krömer, Matouš, Martin Klečka, Lenka Slavětínská, Blanka Klepetářová, and Michal Hocek. "Chemoselective Synthesis of 4,5-Diarylpyrrolo[2,3-d]pyrimidines (6,7-Diaryl-7-deazapurines) by Consecutive Suzuki and Liebeskind-Srogl Cross-Couplings." European Journal of Organic Chemistry 2014, no. 32 (2014): 7203–10. http://dx.doi.org/10.1002/ejoc.201402882.

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30

Riadi, Yassine, Mohammed H. Geesi, Oussama Ouerghi, Rachid Azzallou, Oussama Dehbi, and Saïd Lazar. "Sol-gel TiO2 nanostructures single doped with copper and nickel as nanocatalysts for enhanced performance for the Liebeskind–Srogl reaction." Materials Chemistry and Physics 267 (July 2021): 124607. http://dx.doi.org/10.1016/j.matchemphys.2021.124607.

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31

Zhang, Ze-Ting, Yue Ma, Nai-Li Fan, and Xiang-Guo Hu. "Synthesis of (non-classical) C-acyl-glycosides via Liebeskind–Srogl coupling: Scope, limitation, improved synthesis and antioxidant activity of scleropentaside A." Tetrahedron 92 (July 2021): 132255. http://dx.doi.org/10.1016/j.tet.2021.132255.

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32

Kroemer, Matous, Martin Klecka, Lenka Slavetinska, Blanka Klepetarova, and Michal Hocek. "ChemInform Abstract: Chemoselective Synthesis of 4,5-Diarylpyrrolo[2,3-d]pyrimidines (6,7-Diaryl-7-deazapurines) by Consecutive Suzuki and Liebeskind-Srogl Cross-Couplings." ChemInform 46, no. 16 (2015): no. http://dx.doi.org/10.1002/chin.201516252.

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33

Koley, Moumita, Laurin Wimmer, Michael Schnürch, and Marko D. Mihovilovic. "Pd(0)-Catalyzed Cu(I)-Thiophene-2-carboxylate-mediated Cross-Coupling of Heteroaromatic Thioethers and Boronic Acids-First Liebeskind-Srogl Reaction in Water." Journal of Heterocyclic Chemistry 50, no. 6 (2013): 1368–73. http://dx.doi.org/10.1002/jhet.2005.

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34

Liu, Zheng, Seth G. Thacker, Sara Fernandez-Castillejo, Edward B. Neufeld, Alan T. Remaley, and Robert Bittman. "Synthesis of Cholesterol Analogues Bearing BODIPY Fluorophores by Suzuki or Liebeskind-Srogl Cross-Coupling and Evaluation of Their Potential for Visualization of Cholesterol Pools." ChemBioChem 15, no. 14 (2014): 2087–96. http://dx.doi.org/10.1002/cbic.201402042.

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35

Koley, Moumita, Laurin Wimmer, Michael Schnuerch, and Marko D. Mihovilovic. "ChemInform Abstract: Pd(0)-Catalyzed Cu(I)-Thiophene-2-carboxylate-Mediated Cross-Coupling of Heteroaromatic Thioethers and Boronic Acids - First Liebeskind-Srogl Reaction in Water." ChemInform 45, no. 18 (2014): no. http://dx.doi.org/10.1002/chin.201418152.

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36

Prokopcova, Hana, and C. Oliver Kappe. "ChemInform Abstract: The Liebeskind-Srogl C-C Cross-Coupling Reaction." ChemInform 40, no. 23 (2009). http://dx.doi.org/10.1002/chin.200923248.

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37

Prokopcova, Hana, Leonardo Pisani, and C. Oliver Kappe. "Synthesis of 5-Aroyldihydropyrimidinones via Liebeskind—Srogl Thiol Ester—Boronic Acid Cross-Couplings." ChemInform 38, no. 19 (2007). http://dx.doi.org/10.1002/chin.200719147.

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38

Aguilar-Aguilar, Angelica, and Eduardo Pena-Cabrera. "ChemInform Abstract: Selective Cross-Couplings. Sequential Stille—Liebeskind/Srogl Reactions of 3-Chloro-4-arylthiocyclobutene-1,2-dione." ChemInform 39, no. 12 (2008). http://dx.doi.org/10.1002/chin.200812065.

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