Chiral Bifunctional Ferrocenylphosphine‐Catalyzed Enantioselective Allylic Alkylation of Morita−Baylis−Hillman Carbonates with Pyrazolin‐5‐ones

A chiral bifunctional ferrocenylphosphine catalyzed asymmetric allylic alkylation of Morita−Baylis−Hillman (MBH) carbonates with pyrazolin‐5‐ones was developed. The reaction afforded the desired pyrazolone derivatives in moderate to good yields (up to 80%), and with high enantioselectivities (up to...

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Veröffentlicht in:Asian journal of organic chemistry 2018-12, Vol.7 (12), p.2417-2421
Hauptverfasser: Luo, Wenjun, Song, Dingguo, Fang, Lu, Nian, Sanfei, Hou, Huacui, Ling, Fei, Zhong, Weihui
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Sprache:eng
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Zusammenfassung:A chiral bifunctional ferrocenylphosphine catalyzed asymmetric allylic alkylation of Morita−Baylis−Hillman (MBH) carbonates with pyrazolin‐5‐ones was developed. The reaction afforded the desired pyrazolone derivatives in moderate to good yields (up to 80%), and with high enantioselectivities (up to 98% ee). Enantioselective ironing: A chiral bifunctional ferrocenylphosphine‐catalyzed asymmetric allylic alkylation of Morita−Baylis−Hillman (MBH) carbonates with pyrazolin‐5‐ones was developed. It afforded the desired pyrazolone derivatives in satisfactory yields with high enantioselectivities.
ISSN:2193-5807
2193-5815
DOI:10.1002/ajoc.201800547