Abstract
Synthesis of α-aminophosphonate derivatives via the Kabachnik–Fields reaction is described using 1-(6-hydroxy-2-isopropenyl-1-benzofuran-yl)-1-ethanone, extracted from rhizomes of Petasites hybridus, primary amines and trialkyl phosphites in the presence of ZnO nanoparticles in water at room temperature. This procedure has advantages such as using natural products as precursors, employing water as a green solvent, good yields and easy separation of products.
Acknowledgment
We gratefully acknowledge financial support from the Islamic Azad University of Ardabil.
References
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Supplemental Material:
The online version of this article offers supplementary material (https://doi.org/10.1515/znb-2017-0177).
©2018 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
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Articles in the same Issue
- Frontmatter
- In this Issue
- Does Lewis basicity correlate with catalytic performance in zerovalent group 8 complexes?
- Crystal structure and luminescence properties of a new dinuclear bismuth(III) coordination polymer containing three types of ligands
- Syntheses, structures, and catalytic properties of two arene-ruthenium(II) complexes bearing N-(2-pyridinyl)aminodiphenylphosphine sulfide ligands
- Synthesis, characterization, anticancer and antimicrobial study of arene ruthenium(II) complexes with 1,2,4-triazole ligands containing an α-diimine moiety
- Green synthesis of α-aminophosphonates using ZnO nanoparticles as an efficient catalyst
- Nano-NiZr4(PO4)6 as a superior catalyst for the synthesis of propargylamines under ultrasound irradiation
- Efficient pseudo five-component synthesis of 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1H-pyrazol-5-ol) derivatives promoted by a novel ionic liquid catalyst
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