Phosphine-Catalyzed Asymmetric Tandem Isomerization/Annulation of Allyl Amines with Allenoates: Enantioselective Annulation of a Saturated C–N Bond

Under catalysis by chiral phosphine, an asymmetric isomerization/annulation cascade reaction of allylamines with allenoates was realized. A wide range of γ-substituted allenoates were tolerated to afford chiral pyrroline derivatives in high yields with excellent enantioselectivities. In the reaction...

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Veröffentlicht in:Organic letters 2021-12, Vol.23 (23), p.9173-9178
Hauptverfasser: Zhou, Leijie, Zhang, Xue, Wang, Qijun, Liu, Min, Wang, Wei, Wu, Yongjun, Chen, Liezhong, Guo, Hongchao
Format: Artikel
Sprache:eng
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Zusammenfassung:Under catalysis by chiral phosphine, an asymmetric isomerization/annulation cascade reaction of allylamines with allenoates was realized. A wide range of γ-substituted allenoates were tolerated to afford chiral pyrroline derivatives in high yields with excellent enantioselectivities. In the reaction, isomerization of readily available N-allylamines to reactive aliphatic imines through a 1,4-proton shift is a key step, which circumvents the isolation of highly unstable alkyl N-sulfonylimines.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.1c03483