Relevant bibliographies by topics / Cyclic α-Aminophosphonates

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  1. Journal articles

Academic literature on the topic 'Cyclic α-Aminophosphonates'

Author: Grafiati
Published: 6 September 2023

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Journal articles on the topic "Cyclic α-Aminophosphonates"

1

Odinets, Irina L., Oleg I. Artyushin, Konstantin A. Lyssenko, Nikolay E. Shevchenko, Valentin G. Nenajdenko, and Gerd-Volker Röschenthaler. "Facile synthesis of cyclic α-perfluoroalkyl-α-aminophosphonates." Journal of Fluorine Chemistry 130, no. 7 (July 2009): 662–66. http://dx.doi.org/10.1016/j.jfluchem.2009.05.002.

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2

Odinets, Irina, Oleg Artyushin, Nikolay Shevchenko, Pavel Petrovskii, Valentin Nenajdenko, and Gerd-Volker Röschenthaler. "Efficient Synthesis of Substituted Cyclic α-Aminophosphonates." Synthesis 2009, no. 04 (February 2009): 577–82. http://dx.doi.org/10.1055/s-0028-1083349.

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3

Sobhani, Sara, Elham Safaei, Mozaffar Asadi, Fariba Jalili, and Zahra Tashrifi. "Efficient synthesis of secondary and primary dialkyl α-aminophosphonates catalyzed by tetramethyl-tetra-3,4-pyridinoporphyrazinato copper(II) methyl sulfate under solvent-free conditions." Journal of Porphyrins and Phthalocyanines 12, no. 07 (July 2008): 849–56. http://dx.doi.org/10.1142/s1088424608000248.

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An efficient method for the synthesis of secondary and primary dialkyl α-aminophosphonates under solvent-free conditions by one-pot reaction of aldehydes/ketones, amines/ammonium acetate and trialkyl/diethyl phosphite in the presence of a low catalytic amount of [ Cu (3,4-tmtppa)]( MeSO 4)4(0.16 mol%) as a highly stable and reusable catalyst, is described. By this method, aromatic, aliphatic, cyclic and heterocyclic aldehydes, hindered and cage ketones are converted into their corresponding α-aminophosphonates in good to excellent yields.
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4

Ray Choudhury, Abhijnan, and Santanu Mukherjee. "Enantioselective dearomatization of isoquinolines by anion-binding catalysis en route to cyclic α-aminophosphonates." Chemical Science 7, no. 12 (2016): 6940–45. http://dx.doi.org/10.1039/c6sc02466a.

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Abstract:
An enantioselective dearomatization of isoquinolines has been developed using chiral anion-binding catalysis. This transformation makes use of silyl phosphite as a nucleophile and generates cyclic α-aminophosphonates.
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5

Yan, Zhong, Bo Wu, Xiang Gao, and Yong-Gui Zhou. "Enantioselective synthesis of quaternary α-aminophosphonates by Pd-catalyzed arylation of cyclic α-ketiminophosphonates with arylboronic acids." Chemical Communications 52, no. 72 (2016): 10882–85. http://dx.doi.org/10.1039/c6cc04096a.

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6

Xu, Bo, Gerald Hammond, Junbin Han, and Robert Paton. "Synthesis of Cyclic α-Aminophosphonates through Copper-Catalyzed Enamine Activation." Synthesis 45, no. 04 (January 17, 2013): 463–70. http://dx.doi.org/10.1055/s-0032-1317984.

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7

Yuan, Chengye, Qianyi Chen, and Jinfeng Li. "Sulfinimine-Mediated Asymmetric Synthesis of Acyclic and Cyclic α-Aminophosphonates." Synthesis 2008, no. 18 (September 2008): 2986–90. http://dx.doi.org/10.1055/s-2008-1067247.

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8

Han, Junbin, Robert S. Paton, Bo Xu, and Gerald B. Hammond. "ChemInform Abstract: Synthesis of Cyclic α-Aminophosphonates Through Copper-Catalyzed Enamine Activation." ChemInform 44, no. 26 (June 6, 2013): no. http://dx.doi.org/10.1002/chin.201326176.

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9

Yan, Zhong, Xiang Gao, and Yong-Gui Zhou. "Enantioselective synthesis of quaternary α-aminophosphonates by organocatalytic Friedel–Crafts reactions of indoles with cyclic α-ketiminophosphonates." Chinese Journal of Catalysis 38, no. 5 (May 2017): 784–91. http://dx.doi.org/10.1016/s1872-2067(17)62804-3.

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10

Liu, Yong-Jie, Jin-Shan Li, Jing Nie, and Jun-An Ma. "Organocatalytic Asymmetric Decarboxylative Mannich Reaction of β-Keto Acids with Cyclic α-Ketiminophosphonates: Access to Quaternary α-Aminophosphonates." Organic Letters 20, no. 12 (May 31, 2018): 3643–46. http://dx.doi.org/10.1021/acs.orglett.8b01422.

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