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Highly Chemoselective Rauhut–Currier Reaction between Maleimides and Enones and Dual Phosphine-Mediated One-Pot Synthesis of Bicyclic and Polycyclic Skeletons

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NIAID Data Ecosystem2026-03-08 收录
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https://figshare.com/articles/dataset/Highly_Chemoselective_Rauhut_Currier_Reaction_between_Maleimides_and_Enones_and_Dual_Phosphine_Mediated_One_Pot_Synthesis_of_Bicyclic_and_Polycyclic_Skeletons/2360947
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A highly chemoselective phosphine-catalyzed Rauhut–Currier reaction between maleimides and enones has been realized under very mild conditions, affording the corresponding cross-coupling products in moderate to excellent yields. On the basis of this reaction, an efficient dual phosphine-mediated one-pot synthesis of bicyclic and polycyclic compounds containing a cyclopenta­[c]­pyrrole skeleton has been accordingly developed, which features a tandem sequence of intermolecular Rauhut–Currier reaction and intramolecular Wittig reaction.
创建时间:
2016-02-18
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