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Merck
CN
  • Efficient synthesis of multicyclic spirooxindoles via a cascade Michael/Michael/oxa-Michael reaction of curcumins and isatylidene malononitriles.

Efficient synthesis of multicyclic spirooxindoles via a cascade Michael/Michael/oxa-Michael reaction of curcumins and isatylidene malononitriles.

Organic & biomolecular chemistry (2012-01-11)
Xiao-Gang Yin, Xin-Yun Liu, Zhi-Peng Hu, Ming Yan
摘要

A cascade Michael/Michael/oxa-Michael reaction between curcumins and isatylidene malononitriles has been developed. Multicyclic spirooxindoles were prepared in excellent yields and diastereoselectivities. DMAP was found to catalyze this transformation efficiently under mild reaction conditions.

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Sigma-Aldrich
丙二腈, ≥99%
Sigma-Aldrich
丙二腈, Arxada quality, ≥99.0% (calculated, GC, KF)