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Combinatorial Chemistry. Synthesis, Analysis, Screening. Edited by Günther Jung (guenther.jung@uni-tuebingen.de). Wiley-VCH: Weinheim. 1999. XXXII+602 pp. 268 DM. ISBN 3-527-29869-X
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Molecules 2000, 5(3), 200-207; doi:10.3390/50300200

Chemistry of Pyrones, Part 3: New Podands of 4H-Pyran-4-ones

Department of Organic Chemistry, Faculty of Chemistry, Tabriz University, Tabriz 51664, Iran
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Author to whom correspondence should be addressed.
Received: 2 February 2000 / Accepted: 14 February 2000 / Published: 1 March 2000
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Abstract

New derivatives of 3,5-disubstituted 4H-Pyran-4-one podands (9-15) were prepared by transesterification reaction of dimethyl or diethyl 2,6-dimethyl-4H-pyran-4-one-3,5-dicarboxylate with some glycol, glycol ethers or by nucleophilic substitution of some phenols or glycol ethers with 3,5-bis (bromomethyl)-2,6-diphenyl-4H-pyran-4-one.
Keywords: Podands; 4H-Pyran-4-one; Open-chain crown; Transesterification reaction; Nucleophilic substitution Podands; 4H-Pyran-4-one; Open-chain crown; Transesterification reaction; Nucleophilic substitution
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Shahrisa, A.; Banaei, A. Chemistry of Pyrones, Part 3: New Podands of 4H-Pyran-4-ones. Molecules 2000, 5, 200-207.

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