Relevant bibliographies by topics / Copper catalyzed cascade reaction

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Academic literature on the topic 'Copper catalyzed cascade reaction'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Copper catalyzed cascade reaction"

1

Liang, Lei, Guanyu Yang, Wei Wang, et al. "A Copper-Catalyzed Aerobic Cascade Dehydrogenative- Dehalogenative Reaction." Advanced Synthesis & Catalysis 355, no. 7 (2013): 1284–90. http://dx.doi.org/10.1002/adsc.201300026.

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2

Li, Zhengning, Chongnian Wang та Zengchang Li. "Copper-catalyzed cascade reactions of α,β-unsaturated esters with keto esters". Beilstein Journal of Organic Chemistry 11 (6 лютого 2015): 213–18. http://dx.doi.org/10.3762/bjoc.11.23.

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A copper-catalyzed cascade reaction of α,β-unsaturated esters with keto esters is reported. It features a copper-catalyzed reductive aldolization followed by a lactonization. This method provides a facile approach to prepare γ-carboxymethyl-γ-lactones and δ-carboxymethyl-δ-lactones under mild reaction conditions.
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3

Wang, Lifeng, Qingshan Tian, Chen Bin, and Guozhu Zhang. "Copper-catalyzed radical cascade reaction of isocyanate and ethers." Tetrahedron Letters 60, no. 31 (2019): 2084–87. http://dx.doi.org/10.1016/j.tetlet.2019.07.013.

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4

Zhao, Mi-Na, Zhi-Jing Zhang, Zhi-Hui Ren, De-Suo Yang, and Zheng-Hui Guan. "Copper-Catalyzed Oxidative Cyclization/1,2-Amino Migration Cascade Reaction." Organic Letters 20, no. 10 (2018): 3088–91. http://dx.doi.org/10.1021/acs.orglett.8b01139.

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5

Wen, Qiaodong, Ping Lu, and Yanguang Wang. "Copper-mediated three-component synthesis of 3-cyanoimidazo[1,2-a]pyridines." Chemical Communications 51, no. 84 (2015): 15378–81. http://dx.doi.org/10.1039/c5cc05821j.

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A copper-mediated three-component approach towards the synthesis of 3-cyanoimidazo[1,2-a]pyridines from 2-aminopyridines, acetophenones and benzyl cyanide was developed. This cascade reaction proceeds through a copper-mediated oxidative release of cyanide from benzyl cyanide, a copper-mediated Ortoleva–King reaction, and a copper-catalyzed cyanation.
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6

Zhang, Hong-Yu, Liu-Liang Mao, Bin Yang, and Shang-Dong Yang. "Copper-catalyzed radical cascade cyclization for the synthesis of phosphorated indolines." Chemical Communications 51, no. 19 (2015): 4101–4. http://dx.doi.org/10.1039/c4cc10267c.

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7

Feng, Shangbiao, Jinlai Li, Feifei He та ін. "A copper-catalyzed radical coupling/fragmentation reaction: efficient access to β-oxophosphine oxides". Organic Chemistry Frontiers 6, № 7 (2019): 946–51. http://dx.doi.org/10.1039/c9qo00006b.

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8

Jeyachandran, Rajkumar, Harish Kumar Potukuchi, and Lutz Ackermann. "Copper-catalyzed CuAAC/intramolecular C–H arylation sequence: Synthesis of annulated 1,2,3-triazoles." Beilstein Journal of Organic Chemistry 8 (October 16, 2012): 1771–77. http://dx.doi.org/10.3762/bjoc.8.202.

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Step-economical syntheses of annulated 1,2,3-triazoles were accomplished through copper-catalyzed intramolecular direct arylations in sustainable one-pot reactions. Thus, catalyzed cascade reactions involving [3 + 2]-azide–alkyne cycloadditions (CuAAC) and C–H bond functionalizations provided direct access to fully substituted 1,2,3-triazoles with excellent chemo- and regioselectivities. Likewise, the optimized catalytic system proved applicable to the direct preparation of 1,2-diarylated azoles through a one-pot C–H/N–H arylation reaction.
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9

Huang, Yuanqiong, Zhonglin Guo, Hongjian Song, Yuxiu Liu, and Qingmin Wang. "Silver–copper co-catalyzed cascade intramolecular cyclization/desulfinamide/dehydrogenation: one-pot synthesis of substituted carbazoles." Chemical Communications 54, no. 52 (2018): 7143–46. http://dx.doi.org/10.1039/c8cc03600d.

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10

Zhu, Shangrong, Xuechen Lu, Qiuneng Xu, Jian Li, and Shenghu Yan. "Cu-Catalyzed Cascade Reaction of Isoxazoles with Diaryliodonium Salts for the Synthesis of Acridines." Letters in Organic Chemistry 17, no. 12 (2020): 944–50. http://dx.doi.org/10.2174/1570178617666200225125427.

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A straightforward and efficient synthesis of acridine derivatives via a copper-catalyzed cascade reaction among isoxazoles and diaryliodonium salts is achieved. Various mono-, multi-substituted and 9-substituted acridine derivatives could be obtained in moderate to good yields. The process has gone through tandem double arylation and Friedel-Crafts reactions.
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