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Stereoselective Synthesis of Polysubstituted Cyclopropanes from Poly(ethylene glycol) Supported Pyridinium Ylide

Stereoselective Synthesis of Polysubstituted Cyclopropanes from Poly(ethylene glycol) Supported Pyridinium Ylide
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摘要 Polysubstituted cyclopropanes were efficiently prepared with poly(ethylene glycol)(PEG) as soluble support. The reaction of PEG-supported pyridinium ylide with arylidenemalononitrile(R=CN) or ethyl arylidenecyanoa-cetate(R=COOEt) in the presence of triethylamine(TEA) afforded PEG-supported cyclopropanecarboxylates, which were cleaved by 1% KCN/EtOH to obtain polysubstituted cyclopropanes with exclusive trans-selectivity and good yields. Polysubstituted cyclopropanes were efficiently prepared with poly(ethylene glycol)(PEG) as soluble support. The reaction of PEG-supported pyridinium ylide with arylidenemalononitrile(R=CN) or ethyl arylidenecyanoa-cetate(R=COOEt) in the presence of triethylamine(TEA) afforded PEG-supported cyclopropanecarboxylates, which were cleaved by 1% KCN/EtOH to obtain polysubstituted cyclopropanes with exclusive trans-selectivity and good yields.
出处 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2011年第6期984-987,共4页 高等学校化学研究(英文版)
基金 Supported by the National High Technology Research and Development Program of China(No.2009AA03Z420) the Natural Science Foundation of Hubei Province of China(Nos.2007ABA031,2008CDA078)
关键词 Poly(ethylene glycol) Pyridinium ylide Synthesis CYCLOPROPANE Poly(ethylene glycol) Pyridinium ylide Synthesis Cyclopropane
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