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Synthesis 2003(10): 1569-1573
DOI: 10.1055/s-2003-40511
DOI: 10.1055/s-2003-40511
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York
Poly(ethylene glycol) Supported Liquid-Phase Synthesis of 1,2,4-Oxadiazolines
Weitere Informationen
Received
24 March 2003
Publikationsdatum:
08. Juli 2003 (online)
Publikationsverlauf
Publikationsdatum:
08. Juli 2003 (online)
Abstract
The liquid-phase synthesis of oxadiazolines via 1,3-dipolar cycloaddition reaction on poly(ethylene glycol) support (PEG) is described. 1,3-Dipolar cycloadditions of nitrile oxide generated in situ on soluble polymer with a variety of imines provided a library of 1,2,4-oxadiazolines in good yields and purity. The reactions were run in the homogeneous phase and the synthetic sequences were performed in parallel one-pot fashion. Quantitative conversion in the 1,3-dipolar cycloaddition reaction was verified by 1H NMR analysis. The polymer bound products were isolated in excellent yields by simple precipitation of the soluble support.
Key words
1,3-dipolar cycloaddition - soluble polymer - liquid-phase synthesis - oxadiazolines - poly(ethylene glycol)
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