## Abstract magnified image A library of 1,2,3,7‐tetrasubstituted indolizines has been synthesized using poly(ethylene glycol) (PEG) as soluble polymer support. The PEG‐bound pyridinium salts reacted with alkenes or alkynes in the presence of Et~3~N __via__ 1,3‐dipolar cycloaddition to give PEG‐bo
A facile synthesis of tetrasubstituted 2,3-dihydrofuran derivatives using poly(ethylene glycol) as soluble support
✍ Scribed by Chun Feng; Cuifen Lu; Zuxing Chen; Nianguo Dong; Jiawei Shi; Guichun Yang
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2010
- Tongue
- English
- Weight
- 247 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.372
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✦ Synopsis
Abstract
magnified image
A facile synthesis of tetrasubstitude 2,3‐dihydrofurans has been conducted using poly(ethylene glycol) (PEG) as a soluble polymer support. The PEG‐supported pyridinium ylides react with 3‐arylidene‐2,4‐pentanedione in the presence of triethylamine (TEA) via conjugate addition to form PEG‐supported dihydrofuran derivatives, being cleaved by 1% KCN/EtOH to afford trans‐tetrasubstitude‐2,3‐dihydrofurans, varying from good to excellent yields. J. Heterocyclic Chem., (2010).
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