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Relevant bibliographies by topics / Liebeskind-Srogl coupling

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Journal articles

Academic literature on the topic 'Liebeskind-Srogl coupling'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Liebeskind-Srogl coupling"

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. "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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5

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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6

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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7

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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8

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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9

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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10

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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